Medical Equipment Coordinator Stellenangebote


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Stellenangebote Medical Equipment Coordinator Jobs


Neu Job vor 4 Std. bei Mindmatch.ai gefunden International Atomic Energy Agency

Food Irradiation Specialist (P4)

• AT- 9 Wien [. .. ] safety, the development of standards and guidelines, and the management of nuclear emergency preparedness affecting food and agriculture. Role The Food Irradiation Specialist acts as a technical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] adviser and research coordinator, ensuring the efficient development and implementation of research and training, advising the Section, Division and other IAEA staff on programmatic, scientific and technical matters, and serving as a liaison to provide public outreach on the transfer of irradiation technologies to Member States. Functions/ Key Results Expected Plan and implement coordinated [. .. ] serve in scientific missions and represent the IAEA at relevant meetings. Service the technical cooperation programme by evaluating project requests and assisting with expert assignments, training and the purchase of equipment. Competencies Communication: communicates orally and in writing in a clear, concise and impartial manner, listens and understands others and proposes solutions. Achieving Results: takes initiative in defining realistic outputs and clarifying roles, evaluates results realistically, drawing conclusions from lessons learned. Teamwork: actively contributes to achieving team results and supports team [. .. ] Evaluation may include an assessment exercise followed by a competencybased interview. Candidates seriously considered may be subject to reference and background checks. Appointment Information Appointment is subject to a satisfactory medical report. Staff members may be assigned to any location. Appointees to Professional and higher categories are subject to the IAEA rotation policy; maximum tour of service normally seven years. The IAEA reserves discretion not to make any appointment to this vacancy, to make an appointment at a lower grade, a [. .. ]

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Job am 08.11.2025 bei Mindmatch.ai gefunden Healthcare Businesswomens Association Associate Director-Medical Device Analytical Representative (f/m/d) • AT- 7 Schaftenau Führungs-/ Leitungspositionen [. .. ] Technology Location: Schaftenau, Austria #LI-Hybrid Key Responsibilities As a member of global CMC analytical subteam and device subteam for your project (s) , you are the contact [...]
MEHR INFOS ZUM STELLENANGEBOT[...] person coordinator for all projectspecific analytical tasks related to functional attributes of drugdevice combination products at all levels (from component to drug product to final product) ; plan resource budget for your project (s) Select testing laboratory inline with resource availability, capability and in/ outsourcing strategy, e. g. GDPD, QC, CRO; lead [. .. ] experience, qualifications and individual competencies. We are open for parttime and jobsharing models and support flexible and remote working where possible. Adjustments for Applicants with Disabilities If because of a medical condition, physical disability or a neurodiverse condition you require an adjustment during the recruitment process, please reach out to and let us know the nature of your request as well as your contact information. The support which we can provide will include advice on suitable positions as well as guidance [. .. ] like to request this, please let us know in advance as a note on your CV. Skills Desired Coaching Skills Data Science Environment Experiments Design Health And Safety (Ehs) Laboratory Equipment Manufacturing Process Materials Science Process Simulation Sop (Standard Operating Procedure) Technical Writing Waterfall Model J-18808-Ljbffr 68755897 [. .. ]

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Job am 02.11.2025 bei Mindmatch.ai gefunden International Atomic Energy Agency (IAEA)

Executive Assistant (G5)

• AT- 9 Wien [. .. ] information for nuclear facilities in over 180 States; and technical staff responsible for a wide range of activities including: developing concepts and approaches for implementing safeguards; developing [...]
MEHR INFOS ZUM STELLENANGEBOT[...] and maintaining safeguards equipment; providing analytical and laboratory services for sample analysis; collecting, evaluating and analysing safeguards-relevant information; providing information and communication technology infrastructure and services; and providing programme coordination support. Operations Divisions and the Office for Verification in Iran perform and document safeguards verification activities and conduct analysis and evaluations aimed at [. .. ] prepare meeting minutes and type reports and documents as required. Ensure the Divisions records of all media are maintained, stored and accessible according to corporate standards. As the Records Office Coordinator (ROC) , assign and coordinate Records Office responsibilities, identify and recommend to ARMS (Archives and Records Management Section) process improvements relating to correspondence and records management, liaise with ARMS staff on records management issues, provide information to colleagues on records management standards and practices, facilitate electronic and paper file transfers [. .. ] competencybased interview. Candidates under serious consideration for selection may be subject to reference and background checks as part of the recruitment process. Appointment information Appointment is subject to a satisfactory medical report. Staff members may be assigned to any location. The IAEA retains the discretion not to make any appointment to this vacancy, to make an appointment at a lower grade or with a different contract type, or to make an appointment with a modified job description or for shorter duration [. .. ]

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Neu Job vor 4 Std. bei Jobleads gefunden Food Irradiation Specialist (P4) • Wien [. .. ] safety, the development of standards and guidelines, and the management of nuclear emergency preparedness affecting food and agriculture. Role The Food Irradiation Specialist acts as a technical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] adviser and research coordinator, ensuring the efficient development and implementation of research and training, advising the Section, Division and other IAEA staff on programmatic, scientific and technical matters, and serving as a liaison to provide public outreach on the transfer of irradiation technologies to Member States. Functions/ Key Results Expected Plan and implement coordinated [. .. ] serve in scientific missions and represent the IAEA at relevant meetings. Service the technical cooperation programme by evaluating project requests and assisting with expert assignments, training and the purchase of equipment. Competencies Communication: communicates orally and in writing in a clear, concise and impartial manner, listens and understands others and proposes solutions. Achieving Results: takes initiative in defining realistic outputs and clarifying roles, evaluates results realistically, drawing conclusions from lessons learned. Teamwork: actively contributes to achieving team results and supports team [. .. ] Evaluation may include an assessment exercise followed by a competencybased interview. Candidates seriously considered may be subject to reference and background checks. Appointment Information Appointment is subject to a satisfactory medical report. Staff members may be assigned to any location. Appointees to Professional and higher categories are subject to the IAEA rotation policy; maximum tour of service normally seven years. The IAEA reserves discretion not to make any appointment to this vacancy, to make an appointment at a lower grade, a [. .. ]

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Job am 08.11.2025 bei Jobleads gefunden

Associate Director-Medical Device Analytical Representative (f/m/d)

• Schaftenau, Tirol Führungs-/ Leitungspositionen [. .. ] Technology Location: Schaftenau, Austria #LI-Hybrid Key Responsibilities As a member of global CMC analytical subteam and device subteam for your project (s) , you are the contact [...]
MEHR INFOS ZUM STELLENANGEBOT[...] person coordinator for all projectspecific analytical tasks related to functional attributes of drugdevice combination products at all levels (from component to drug product to final product) ; plan resource budget for your project (s) Select testing laboratory inline with resource availability, capability and in/ outsourcing strategy, e. g. GDPD, QC, CRO; lead [. .. ] experience, qualifications and individual competencies. We are open for parttime and jobsharing models and support flexible and remote working where possible. Adjustments for Applicants with Disabilities If because of a medical condition, physical disability or a neurodiverse condition you require an adjustment during the recruitment process, please reach out to and let us know the nature of your request as well as your contact information. The support which we can provide will include advice on suitable positions as well as guidance [. .. ] like to request this, please let us know in advance as a note on your CV. Skills Desired Coaching Skills Data Science Environment Experiments Design Health And Safety (Ehs) Laboratory Equipment Manufacturing Process Materials Science Process Simulation Sop (Standard Operating Procedure) Technical Writing Waterfall Model #J-18808-Ljbffr 68845948 [. .. ]

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Job am 06.11.2025 bei Jobleads gefunden Principal Customer Success Manager, DACH • München, Bayern [. .. ] Proactively identify risks and new opportunities for product crosssell and upsell, leveraging your deep understanding of the customers business and industry. Cross Functional Orchestration: Act as the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] internal champion and coordinator for the customer, mobilizing and leading extended teams (Sales, Solutions Engineers, Product, Support, and Engineering) to ensure seamless delivery, issue resolution, and a consistently highquality experience. Product Expertise: Maintain a strong understanding of the Cloudflare Connectivity Cloud, confidently discussing technical solutions around Security (DDo S, WAF, Zero Trust) and Performance (CDN, [. .. ] regard to their, or any other persons, perceived or actual race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, national origin, ancestry, citizenship, age, physical or mental disability, medical condition, family care status, or any other basis protected by law. We are an AA/ Veterans/ Disabled Employer. Cloudflare provides reasonable accommodations to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job. Examples of reasonable accommodations include, but are not limited to, changing the application process, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. If you require a reasonable accommodation to apply for a job, please contact us via email at or via mail at 101 Townsend St. San Francisco, CA 94107. #J-18808-Ljbffr 68619515 [. .. ]

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Job am 26.10.2025 bei Jobleads gefunden

Special Operations Physical Therapist (Baumholder, Germany)

• Stuttgart, Baden- Württemberg [. .. ] injections, and referrals to specialty providers. Directly supervise the PT Tech, PT Assistant, and/or Certified Athletic Trainer within their scope of practice as directed by the HP [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Program Manager/ Coordinator. Participate in periodic meetings with HP and POTFF to review patient care and identify improvement opportunities. Serve as an advisor on sports medicine, injury prevention, rehabilitation, and human performance research for the HP Program Manager/ Coordinator. Serve as an advisor for administrative matters, purchasing supplies, equipment, and supplemental fiscal requests. Conduct equipment, product, and literature reviews to keep the HP program current. Provide input for developing and utilizing required databases. Conduct peer (record) reviews for HP staff as directed by governing credentialing bodies and local medical oversight processes. Assist in developing and updating criteriabased job descriptions and performance standards. Assist in developing and maintaining clinical practice guidelines across HP Training Centers and associated facilities. Assist with short and longterm fiscal planning and submit input to the HP Program Manager/ Coordinator. Attend and participate in meetings with [. .. ]

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Job am 25.10.2025 bei Jobleads gefunden Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience • Frankfurt, Hesse Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities [. .. ]

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Job am 19.10.2025 bei Jobleads gefunden

Principal Customer Success Manager, DACH

• München, Bayern [. .. ] Proactively identify risks and new opportunities for product crosssell and upsell, leveraging your deep understanding of the customers business and industry. Cross Functional Orchestration: Act as the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] internal champion and coordinator for the customer, mobilizing and leading extended teams (Sales, Solutions Engineers, Product, Support, and Engineering) to ensure seamless delivery, issue resolution, and a consistently highquality experience. Product Expertise: Maintain a strong understanding of the Cloudflare Connectivity Cloud, confidently discussing technical solutions around Security (DDo S, WAF, Zero Trust) and Performance (CDN, [. .. ] regard to their, or any other persons, perceived or actual race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, national origin, ancestry, citizenship, age, physical or mental disability, medical condition, family care status, or any other basis protected by law. We are an AA/ Veterans/ Disabled Employer. Cloudflare provides reasonable accommodations to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job. Examples of reasonable accommodations include, but are not limited to, changing the application process, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment. If you require a reasonable accommodation to apply for a job, please contact us via email at or via mail at 101 Townsend St. San Francisco, CA 94107. #J-18808-Ljbffr 66550843 [. .. ]

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Job am 02.10.2025 bei Jobleads gefunden Instructor Operator Team Lead • Vilseck, Bayern Führungs-/ Leitungspositionen [. .. ] cybersecurity, intelligence gathering and analysis, and simulation and exercise support, as well as aviation flight logistics support and unmanned aerial vehicle support. Summary: We are seeking a [...]
MEHR INFOS ZUM STELLENANGEBOT[...] dedicated and experienced Medical Instructor/ Operator Team Lead (I/ O-Team Lead) to join the Medical Simulation Training Center (MSTC) Instructor Operator Support Services (MIOSS) team. The I/ O-Team Lead role provides training support services for the Medical Simulation Training Center (MSTC) , which carries out medical instruction and skill validation for the [. .. ] MTN on schedule. Assist with and or complete administrative duties for all POIs as instructed by Nisgaa MOSTT. Conduct basic preventative maintenance on low and high-fidelity medical training manikins/ equipment task/ trainers. Perform PMCS (daily, weekly, monthly and annual maintenance) on all equipment and document it appropriately. Report any inoperable equipment to the TOR. Troubleshoot all high fidelity training manikins with the vendor (when under warranty) and send out for service when needed. Work with the appropriate ATMP contact for maintenance on out-of-warranty manikins/ task trainers. Conduct weekly Class VIII and durable item inventories and regularly report statuses to the Technical Office Representative (TOR) and Course Coordinator. Work with the training unit to assist the unit in preparing for training to include equipment use, preparation and clean up. Set up and breakdown all required training equipment for each POI instructed. Provide course rosters and sign in sheets to the Course Coordinator. Prepare all student course handouts. Provide [. .. ]

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Job am 26.09.2025 bei Jobleads gefunden

Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience

• Essen, Nordrhein- Westfalen Overview Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is [...]
MEHR INFOS ZUM STELLENANGEBOT[...] to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities [. .. ]

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Job am 20.09.2025 bei Jobleads gefunden Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, [...]
MEHR INFOS ZUM STELLENANGEBOT[...] pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, [. .. ] compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities [. .. ]

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Job gestern bei Neuvoo gefunden Maersk

Trainer Quality Coordinator

• Philippsburg, Baden- Württemberg Job Summary We are looking for a Trainer Quality Coordinator to help our warehouse teams grow their skills and ensure our daily operations run smoothly. In this role, you [...]
MEHR INFOS ZUM STELLENANGEBOT[...] will support training activities, help maintain high-quality standards, and contribute to continuous improvement initiatives across our contract logistics operations. This position is ideal for someone who enjoys working with people, has a good eye for detail, and wants to develop their career in logistics. Key Responsibilities Training Development Deliver onboarding and basic operational training (safety, equipment handling, receiving, picking, packing, inventory, shipping) . Help create and update training materials such as SOPs, work instructions, presentations, and job aids. Maintain training records, certifications (e. g. , forklift/ MHE) , and skill matrices. Support refresher training and day-to-day coaching on warehouse processes. Provide feedback on training [. .. ] is an equal opportunities employer and welcomes applicants without regard to race, colour, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, pregnancy or parental leave, veteran status, gender identity, genetic information, or any other characteristic protected by applicable law. We will consider qualified applicants with criminal histories in a manner consistent with all legal requirements. We are happy to support your need for any adjustments during the application and hiring [. .. ]

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Job vor 2 Tagen bei Neuvoo gefunden West Pharmaceutical Services Coordinator, Laboratory • Eschweiler, North Rhine- Westphalia [. .. ] with corrective action when necessary. Leads regular team meetings to resolve any obstacles or issues and to align on priorities. Is proficient in the use and maintenance [...]
MEHR INFOS ZUM STELLENANGEBOT[...] of laboratory test equipment necessary for conducting root-cause investigations. Provides training of new investigators/ analysts on the processes and use of laboratory equipment. Assists with the creation, review and approval of investigation reports. Creates a safe work environment through identifying and resolving potential safety hazards; maintaining a clean, neat, and safe work environment; [. .. ] project management organization. Self-reliant, diligent, flexible (with working time to fulfill requirements of a global role) . Clear communication (fluent in written and verbal English required) . Background in medical device or pharmaceutical industry. Knowledge of lean manufacturing and operational excellence concepts. Able to comply with the companys safety policy at all times. Able to comply with the companys quality policy at all times. Travel Requirements 5: Up to 13 business days per year Physical Requirements Sedentary-Exerting up to [. .. ]

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Job vor 11 Tagen bei Neuvoo.com gefunden PELI Products

HR Coordinator

• Crottendorf Were Hiring: Human Resources Coordinator Location : Crottendorf, Germany Company : Peli Who We Are At Peli, we engineer products that stand up to the worlds toughest conditionsbecause the [...]
MEHR INFOS ZUM STELLENANGEBOT[...] people who rely on us do too. For nearly 50 years, weve been a trusted partner for military personnel, first responders, outdoor adventurers, and innovators who [. .. ] 11 offices, 4 manufacturing facilities, and 4 custom case centers, we create high-performance protective solutions that ensure our customers can focus on what matters most. Whether its transporting critical medical supplies, securing mission-essential equipment, or keeping expedition gear safe, Peli products are Built to Protect to Equip for the Mission. At Peli, your work has a real-world impact. Youll be part of a team driven by innovation, craftsmanship, and the shared belief that when the mission is critical, failure isnt an option. If [. .. ]

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Job am 14.10.2025 bei Neuvoo.com gefunden Medpace Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience • Essen Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities [. .. ]

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Job am 14.10.2025 bei Neuvoo.com gefunden Medpace Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience • Stuttgart Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities [. .. ]

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Job am 14.10.2025 bei Neuvoo.com gefunden Medpace Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience • Berlin Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities [. .. ]

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Job am 14.10.2025 bei Neuvoo.com gefunden Medpace Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience • Cologne Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities [. .. ]

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Job am 14.10.2025 bei Neuvoo.com gefunden Medpace Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities [. .. ]

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Job am 14.10.2025 bei Neuvoo.com gefunden Medpace Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience • Munich Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities [. .. ]

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Job am 14.10.2025 bei Neuvoo.com gefunden Medpace Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience • Düsseldorf Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities [. .. ]

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Job am 04.10.2025 bei Neuvoo.com gefunden Medpace Clinical Research Associate (Home-Based) - Clinical Research Coordinator Experience • Hamburg Medpace is a full-service clinical contract research organization (CRO) . We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to [...]
MEHR INFOS ZUM STELLENANGEBOT[...] accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, [. .. ] Research Coordinators wanted at Medpace Become a CRA and join our growing team This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a [. .. ] compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff; Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements; On-site and virtual/ remote monitoring activities [. .. ]

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Job vor 14 Tagen bei Europeanlanguagejobs.com gefunden SAP Administrative Coordinator-German Speaking (Entry level) • Budapest, Hungary Homeoffice möglich [. .. ] energy cleaner and better and how you can play your part in our world-class team? Join our Global Customer Care Team and advance your career as a [...]
MEHR INFOS ZUM STELLENANGEBOT[...] SAP Admin Coordinator German Speaking (Entry level) In this role You will: Review vendor proposals to extract data and build purchase requisitions in SAP Monitor purchase orders for accuracy and alignment with requisitions Verify invoices and goods receipts; coordinate timely invoice processing with BP Accenture Track vendor change orders and update change order [. .. ] reporting is good to have Offer: At bp, we provide the following environment benefits to you: Different bonus opportunities based on performance, wide range of cafeteria elements Life health insurance, medical care package Flexible working schedule: home office up to 2 days/ week, based on team agreement Opportunity to build up long term career path and develop your skills with wide range of learning options Family friendly workplace e. g. : Extended parental leave, Mother-baby room Employees wellbeing programs e. [. .. ] to join our social communities and networks Chill-out and collaboration spaces in our beautiful Budapest Agora and Szeged offices e. g. : Play Zones, Office massage, Sport and music equipment Assets like phone for private usage and company laptop are provided from the first day of employment with other equipment if requested bp Hungary won the Most Attractive Employer 2024 Award (SSC/ BSC sector) fourth time in a row at Pw Cs annual employer research. Come and join us 70118518 [. .. ]

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Häufig gestellte Fragen

Wieviel verdient man als Medical equipment coordinator pro Jahr?

Als Medical equipment coordinator verdient man zwischen EUR 45.000,- bis EUR 70.000,- im Jahr.


Wieviele offene Stellenangebote gibt es für Medical Equipment Coordinator Jobs bei unserer Jobsuche?

Aktuell gibt es auf JobRobot 24 offene Stellenanzeigen für Medical Equipment Coordinator Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Medical Equipment Coordinator Jobs?

Aktuell suchen 8 Unternehmen nach Bewerbern für Medical Equipment Coordinator Jobs.


Welche Unternehmen suchen nach Bewerbern für Medical Equipment Coordinator Stellenangebote?

Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Medical Equipment Coordinator Stellenangebote:


  • Medpace (8 Jobs)
  • International Atomic Energy Agency (1 Job)
  • Healthcare Businesswomens Association (1 Job)
  • Maersk (1 Job)
  • West Pharmaceutical Services (1 Job)


In welchen Bundesländern werden die meisten Medical Equipment Coordinator Jobs angeboten?

Die meisten Stellenanzeigen für Medical Equipment Coordinator Jobs werden derzeit in Nordrhein-Westfalen (4 Jobs), Bayern (3 Jobs) und Baden-Württemberg (3 Jobs) angeboten.


Zu welchem Berufsfeld gehören Medical Equipment Coordinator Jobs?

Medical Equipment Coordinator Jobs gehören zum Berufsfeld Medizintechnik.


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Dauer: 0.0417 s., Vers. V.2025-d-2008-Ind-141