37 Jobs für Clinical Data Coordinator
Stellenangebote Clinical Data Coordinator Jobs
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Senior Clinical Trial Assistant
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate (CRA I) / Senior
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 7 Tagen bei Jooble gefunden
Abb Vie
• Wiesbaden
Work-Life-Balance
[. .. ] visit us at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in accordance with local regulations, Good Clinical Practices [. .. ] equivalent work experience. One year of clinically-related experience in a medical profession, pharmaceutical, or diagnostic company is preferred. Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. with a diverse work environment where you can have a real impact with an attractive [. .. ]
Job vor 8 Tagen bei Jooble gefunden
Abb Vie
Clinical Research Associate I
• Wiesbaden
Work-Life-Balance
[. .. ] at. Follow abbvie on X, Facebook, Instagram, You Tube, Linked In and Tik Tok. Job Description Supports in the in-house organization, management and execution of projects to [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] ensure the clinical trials are conducted, recorded, and reported in accordance with the protocol, federal regulations and applicable local regulations, Good Clinical Practices (GCPs) , ICH Guidelines, Abb Vie Standard Operating Procedures (SOPs) , Monitoring Plans, and to quality standards in conducting clinical research. Participates in the study startup activities and site opening activities as well as study conduct and site closure tasks. Manages the activities of clinical investigative sites across multiple protocols and multiple therapeutic areas, with appropriate supervision. Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Ensures safety and protection of study subjects. Supports and/or conducts (accompanied) site qualification, initiation, interim monitoring and study closeout visits for Phase 1-4 studies in [. .. ] Current knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials is preferred Knowledge of conducting industry-sponsored clinical research (e. g. Clinical study coordinator/ data manager, clinical trial assistant (or equivalent) , regulatory document specialist) is preferred. Knowledge related to ICH/ GCP Guidelines and applicable local regulations is preferred. Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Ability to work, [. .. ]
Job vor 14 Tagen bei Jooble gefunden
Thermo Fisher Scientific
• Karlsruhe
[. .. ] safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future. Location/ Division Specific Information Our clinical department defines, develops and delivers clinical programmes. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants. Discover Impactful Work: PPD clinical research services mission is to improve health. It starts as an idea to cure. It becomes a [. .. ]
Job vor 14 Tagen bei Jooble gefunden
rockITdata
Regional Education Coordinator-Traumatic Brain Injury
• Landstuhl
[. .. ] by Innovation and built on Trust, rock ITdata is a unique SDVOSB services company that partners with leading commercial healthcare/ life sciences organizations on cutting edge innovations-think [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] AI, automation and data transformation. We then bring those commercially tested solutions to government entities to deliver predictable, measurable impact for the American taxpayer and consumer. rock ITdata is seeking a Regional Education Coordinator to join our team to support brain health and traumatic brain injury (TBI) education initiatives across a healthcare-focused environment. This role is ideal for an experienced healthcare educator who is passionate about advancing awareness, prevention, treatment, and rehabilitation of traumatic brain injury. The Regional Education Coordinator will be an onsite position. Key Responsibilities: Assist in the development and delivery of traumatic brain injury (TBI) educational initiatives for healthcare teams. Ensure healthcare providers are informed of and understand current clinical standards of care and best practices related to TBI. Collaborate closely with multidisciplinary clinical teams to provide educational opportunities supporting coordinated care for individuals with TBI. Deliver education programs and informational sessions on TBI to patients, families, caregivers, healthcare professionals, and community audiences. Assist in the design and implementation of [. .. ]
Job am 23.01.2026 bei Jooble gefunden
University of Maryland Global Campus
• Homeoffice
Werkstudenten
Student Wellness Basic Needs
Coordinator (Non-
Clinical) Office of Student Affairs Part Time (19hrs a week) , Non-Exempt Contingent 1 Remote UMGC seeks a compassionate, solution-focused professional to serve [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as Coordinator of Wellness Basic Needs within Global Student Support Services. This role supports a global population of adult learners by reducing barriers related to wellness, [. .. ] Build and maintain partnerships with Financial Aid, Global Military Operations, Title IX, Accessibility Services, the Behavioral Intervention Team, and other student support units. Collect and analyze student feedback and service data to drive continuous improvement and surface actionable trends. Support department-wide initiatives advancing equity, belonging, and student success. Required Education Experience Bachelor s degree from a regionally accredited institution in a related field. One (1) year of experience in student support, wellness coordination, or related roles. Strong communication, organizational, and [. .. ]
Job am 20.01.2026 bei Jooble gefunden
KBR
Special Operations Physical Therapist (Baumholder, Germany)
• Stuttgart
[. .. ] following services in support of POTFFs HP program for SOF personnel, with the priority on SOF Operators and Direct Combat Support personnel: Provide neuro-musculoskeletal injury care, utilizing [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] approved supplemental clinical privileges including the ordering of images, laboratory tests, pharmaceuticals, dry needling, acupuncture, joint injections and aspirations, and referrals to specialty providers. If directed by HP Program Manager and/or Coordinator, directly supervise the PT Tech, PT Assistant, and/or Certified Athletic Trainer (ATC) within their scope of practice. Participate in periodic meetings with HP and POTFF for reasons such as, but not limited to, reviewing care provided to patients. Identify opportunities for improvement. Serve as an advisor to the HP [. .. ] scope of the PT position description, as assigned by the HP program Manager and/or Coordinator and/or required by USSOCOM HQ and its POTFF staff. Collect and report all data as requested by the HP program Manager and/or Coordinator and required by USSOCOM HQ and its POTFF staff. Proficiently utilize computers, software, and technologies as required and requested by the HP program Manager and/or Coordinator and required by USSOCOM HQ and its POTFF staff. Required Education/ Experience/ Skills/ [. .. ]
Job am 17.01.2026 bei Jooble gefunden
Alira Health
• München
[. .. ] team dedicated to innovation and initiative, where physical walls and different time zones dont limit, but encourage, collaboration. The Project Manager (PM) is an important member of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the Alira Health Clinical team. Manages clinical study functions, which may include investigational supply, IWRS/ IXRS, data management, biostatistics, pharmacovigilance, and central laboratory. Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates. Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/ form templates, study manuals and plans, site binders, etc. Presents [. .. ]
Job am 21.01.2026 bei Jooble gefunden
Doctolib GmbH
Talent Acquisition Coordination Intern (x/ f/m)
• Berlin
[. .. ] the Netherlands, we re reinventing how care is delivered through a new generation of AI-powered technologies and services. Our Operating System supports health professionals in all their [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] activities, from clinical, financial, to admin and care cooperation. Our Health Companion helps people prevent health problems, detect risks earlier, access care faster, and better follow treatments. Today, over 90 million people use Doctolib to manage their health and find care, while 420K health professionals use Doctolib to focus on what matters most: caring for patients. Your tasks What you ll do We are looking for a Talent Acquisition Coordinator to join the Tech Product Recruiting Team in our Berlin office. As a Coordinator, you ll focus on three essential areas: delivering exceptional candidate experience, mastering complex tech product interview scheduling, and continuously improving our interview processes. In this role, you ll gain comprehensive insight into recruitment while applying your [. .. ] let us know for support during the hiring process. Join us in building the healthcare we all dream of All information provided is processed by Doctolib for application management. For data processing details, click here. Please contact hr. dataprivacy (at) doctolib. com for inquiries or to exercise your rights. The interview process Before you read on if you don t have the exact profile described below, but you feel this job description matches your skill set, we still encourage you to [. .. ]
Job am 14.01.2026 bei Jooble gefunden
IQVIA
• Frankfurt am Main
Führungs-/ Leitungspositionen
JOIN US ON OUR EXCITING JOURNEY IQVIA is The Human
Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. This Clinical Data Team Lead will be responsible for managing end-to-end delivery of data management services for single/ multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products [. .. ] g. , timelines, financial, process, resource Maintain strong customer relationships Ensure open communications with customer and Quintiles management to manage and meet contractual obligations Service Management Meet with Data Operations Coordinator (DOC) and/or Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders Support DM service delivery with comprehensive DM process and technical expertise in executing projects Serve [. .. ]
Job vor 3 Tagen bei Mindmatch.ai gefunden
Residential Transitions
Program Manager-Waiver Case Management (Ramsey County)
• AT- 4 Berg
[. .. ] a closely related field. Be a graduate from an accredited fouryear college with a major in any field and 2000 hours of experience as a social worker/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] case manager/ care coordinator in a public or private social service agency. A public health or registered nurse providing case management must be licensed under Minn. Stat. 148.171148.285. At least two (2) years of management experience. A background in Waivered Case Management. Knowledge of community resources and how to access them. Willingness [. .. ] Holidays : 7 companypaid holidays + 1 floating holiday. Retirement : 401 (k) with company matching contribution. Health Benefits : Medical, dental, and vision insurance. Professional Growth : CEU courses, clinical supervision, and monthly paid trainings relevant to services provided. Career Advancement Opportunities : Grow within RTI. Compensation 55, 000.00-70, 000.00 per year Type Full Time Location: Ramsey County Physical Mental Requirements Walk, stand, sit, bend, climb stairs, and perform crisis prevention/ intervention techniques. Use hands for writing, typing, data entry. Lift up to 40 lbs. and occasionally exert physical effort during duties. Maintain vision and hearing necessary for reading charts, operating office equipment, using a computer, and driving a vehicle. Be the difference by making a difference. Advance your career in mental health today and change someones life tomorrow [. .. ]
Job vor 3 Tagen bei Jobleads gefunden
• Berg, Oberösterreich Oberoesterreich
[. .. ] a closely related field. Be a graduate from an accredited fouryear college with a major in any field and 2000 hours of experience as a social worker/ [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] case manager/ care coordinator in a public or private social service agency. A public health or registered nurse providing case management must be licensed under Minn. Stat. 148.171148.285. At least two (2) years of management experience. A background in Waivered Case Management. Knowledge of community resources and how to access them. Willingness [. .. ] Holidays : 7 companypaid holidays + 1 floating holiday. Retirement : 401 (k) with company matching contribution. Health Benefits : Medical, dental, and vision insurance. Professional Growth : CEU courses, clinical supervision, and monthly paid trainings relevant to services provided. Career Advancement Opportunities : Grow within RTI. Compensation 55, 000.00-70, 000.00 per year Type Full Time Location: Ramsey County Physical Mental Requirements Walk, stand, sit, bend, climb stairs, and perform crisis prevention/ intervention techniques. Use hands for writing, typing, data entry. Lift up to 40 lbs. and occasionally exert physical effort during duties. Maintain vision and hearing necessary for reading charts, operating office equipment, using a computer, and driving a vehicle. Be the difference by making a difference. Advance your career in mental health today and change someones life tomorrow [. .. ]
Job vor 7 Tagen bei Jobleads gefunden
Clinical Research Associate-Pathology
• Mannheim, Baden- Württemberg
Ready to be the heartbeat of medical research? Join our client as a Study
Coordinator and assist in turning innovative science into life-changing care R D Partners is seeking [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] a Clinical Research Associate to support the planning, coordination, and execution of clinical research studies. You will work closely with study sites to ensure compliance with protocols, regulations, and best practices. This role involves collaboration with cross-functional teams and offers an opportunity to contribute to impactful research projects. Please note that [. .. ] Review and develop study-related documents, such as protocols and site-specific templates. Collaborate with internal teams to ensure smooth study execution. Conduct site visits to monitor progress and validate data. Ensure compliance with regulations, guidelines, and standard procedures. Build strong relationships with team members and stakeholders. Key Skills and Requirements: Bachelors degree in a scientific field or equivalent education and experience. Knowledge of clinical research processes and regulatory requirements. Strong organizational and communication skills. Ability to work collaboratively in diverse [. .. ]
Job vor 8 Tagen bei Jobleads gefunden
• Stein, Baden- Württemberg
[. .. ] too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together. We [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] are hiring a Clinical Research Associate III (m/f/d) Location: EMEA (Flexible) . Your Strength Minimum of 4 years of advanced experience in clinical research monitoring In-depth knowledge of regulations and guidelines related to clinical trials on human subjects (e. g. , ISO 14155, GCP, MDR, EU, FDA) Ability to manage 1015 [. .. ] closure Excellent communication skills for site interaction, training, and issue resolution Strong collaboration and mentorship abilities CRA IIIs are expected to guide junior team members Handson experience with monitoring systems, data verification, and compliance tracking Strong organizational skills and the ability to manage multiple priorities Willingness to travel for site visits and meetings Fluency in German and English is required. Proficiency in the language of one of Germanys neighboring countries is an advantage, to support potential cross-border monitoring activities. Your [. .. ] safety and protocol adherence Conduct site training, initiate visits, and support audit/ inspection readiness Collaborate with other departments such as Data Management, Clinical Operations, and Medical Affairs Support investigator and coordinator meetings, and provide training or presentations as needed Mentor junior CRAs and contribute to continuous process improvement Participate in CAPA execution, audits, and ongoing quality assurance activities Our Strength A purpose-driven Clinical Affairs team committed to quality and patient safety Onboarding and development in a structured, supportive environment Exposure [. .. ]
Job vor 11 Tagen bei Jobleads gefunden
Clinical Research Associate III (m/f/d)
• Hechingen, Baden- Württemberg
[. .. ] too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together. We [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] are hiring a Clinical Research Associate III (m/f/d) Location: EMEA (Flexible) Your Strength Minimum of 4 years of advanced experience in clinical research monitoring In-depth knowledge of regulations and guidelines related to clinical trials on human subjects (e. g. , ISO 14155, GCP, MDR, EU, FDA) Ability to manage 1015 study [. .. ] closure Excellent communication skills for site interaction, training, and issue resolution Strong collaboration and mentorship abilities CRAs are expected to guide junior team members Hands-on experience with monitoring systems, data verification, and compliance tracking Strong organizational skills and the ability to manage multiple priorities Willingness to travel for site visits and meetings Fluency in German and English is required. Proficiency in the language of one of Germanys neighboring countries is an advantage, to support potential cross-border monitoring activities. Your [. .. ] safety and protocol adherence Conduct site training, initiate visits, and support audit/ inspection readiness Collaborate with other departments such as Data Management, Clinical Operations, and Medical Affairs Support investigator and coordinator meetings, and provide training or presentations as needed Mentor junior CRAs and contribute to continuous process improvement Participate in CAPA execution, audits, and ongoing quality assurance activities Our Strength A purpose-driven Clinical Affairs team committed to quality and patient safety Onboarding and development in a structured, supportive environment Exposure [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Düsseldorf, Nordrhein- Westfalen
Freiberuflich
Overview Are you looking to drive groundbreaking medical research and make a real impact? Join our client and lead the way in advancing
clinical research Proclinical is supporting a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] client who is seeking an experienced Freelance Clinical Study Coordinator for an on-site assignment in North Rhine-Westphalia, Germany. This is a 6-month freelance contract, with the possibility of renewal, requiring 2-3 days per week on site, with an immediate start date. Responsibilities Clinical data entry Query resolution Management of patient travel cost reimbursement Key Skills and Requirements Proficiency in clinical data entry and query resolution processes. Strong organizational skills and attention to detail. Ability to manage patient-related financial processes effectively. Flexibility to work on-site 2-3 days per week. Application information If [. .. ]
Job am 21.01.2026 bei Jobleads gefunden
Field Data Collection Specialist Surveyor
• Hamburg
Field
Data Collection Specialist Surveyor Join to apply for the Field Data Collection Specialist Surveyor role at TSMG Holding Field Data Collection Specialist Surveyor 9 months ago Be among [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the first 25 applicants Join to apply for the Field Data Collection Specialist Surveyor role at TSMG Holding Company description: Terry Soot Management [. .. ] Management and Manufacturing Industries Outsourcing and Offshoring Consulting Referrals increase your chances of interviewing at TSMG Holding by 2x Sign in to set job alerts for Field Specialist roles. Field Clinical Specialist, Transcatheter Mitral Tricuspid Therapies OEM Field Support Integration Engineer Talent Pool: Field Service Engineer/ Technician (d/f/m) for Diagnostics and Life Sciences in DACH region Field Technical Engineer/ Applikationsspezialist (w/m/d) Elektrophysiologie-Region Hamburg/ Hannover Learning and Development Specialist (all genders) Sales Operations Field Force Coordinator (gn) Field Clinical Specialist Central Lower Saxony-Nurse Biomedical Full time/ Part time Account Leader Energy Resources (w/m/d) Clinical Specialist (m/w/d) VELYS Robotics-Location: Hessen/ NRW Technical Training Program Developer Wind Turbines (d/w/m) Zoiss Engineering Gmb H Senior Compensation Benefits Specialist (all genders) Claims Restructuring [. .. ]
Job am 21.01.2026 bei Jobleads gefunden
Data Team Lead/Senior Data Team Lead (m/w/D)
• Berlin
Führungs-/ Leitungspositionen
JOIN US ON OUR EXCITING JOURNEY IQVIA is The Human
Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward. This Clinical Data Team Lead will be responsible for managing end-to-end delivery of data management services for single/ multi-service projects, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products [. .. ] g. , timelines, financial, process, resource Maintain strong customer relationships Ensure open communications with customer and Quintiles management to manage and meet contractual obligations Service Management Meet with Data Operations Coordinator (DOC) and/or Data Operations team members on a regular basis to ensure milestones meet timelines and quality deliverables Establish strong communications with Data Operations team, functional leads, project managers and all other stake holders Support DM service delivery with comprehensive DM process and technical expertise in executing projects Serve [. .. ]
Job am 19.01.2026 bei Jobleads gefunden
Clinical Research Associate III
• Berlin
[. .. ] counts, too: As an important link in the chain, you make a contribution to saving lives together with us. Contribute your strengths and let us grow together. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] We are hiring Clinical Research Associate III (m/f/d) Location: EMEA (Flexible) Your strength Minimum of 4 years of advanced experience in clinical research monitoring In-depth knowledge of regulations and guidelines related to clinical trials on human subjects (e. g. , ISO 14155, GCP, MDR, EU, FDA) Ability to manage 1015 study [. .. ] closure Excellent communication skills for site interaction, training, and issue resolution Strong collaboration and mentorship abilities CRA IIIs are expected to guide junior team members Handson experience with monitoring systems, data verification, and compliance tracking Strong organizational skills and the ability to manage multiple priorities Willingness to travel for site visits and meetings Fluency in German and English is required. Proficiency in the language of one of Germanys neighboring countries is an advantage, to support potential crossborder monitoring activities. Your contribution [. .. ] safety and protocol adherence Conduct site training, initiate visits, and support audit/ inspection readiness Collaborate with other departments such as Data Management, Clinical Operations, and Medical Affairs Support investigator and coordinator meetings, and provide training or presentations as needed Mentor junior CRAs and contribute to continuous process improvement Participate in CAPA execution, audits, and ongoing quality assurance activities Our strength A purposedriven Clinical Affairs team committed to quality and patient safety Onboarding and development in a structured, supportive environment Exposure to [. .. ]
Job am 31.10.2025 bei Jobleads gefunden
Associate Director, Global Regulatory Affairs, Advertising and Promotion
• Glattbrugg, Zürich
Führungs-/ Leitungspositionen
[. .. ] review, approval, and implementation of medical and commercial materials. You will be product or project business lead for global CMRP at Takeda CMRP Meeting Chair-pausing to communicate [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] comments to coordinator, diffusing team disputes, serving as a dependable negotiator, keeping team focus on our ultimate stakeholders which are the patients who trust us to do the right thing, and overseeing escalation steps if MLR cannot come to alignment or if there is new data or campaigns that require senior level management input or alignment. Strategic business partner from clinical trial development through the marketing maintenance phase of a product lifecycle Subject matter expert on EFPIA, IFPMA, and FDA code/ regs, guidance, industry standards, complaints/ violations, and innovative promotional platforms Act as a strategic partner spanning clinical trial development through the marketing and maintenance phases of the product lifecycle. Regulatory [. .. ]
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. [. .. ] 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 other POTFF staff and medical providers as required. Ensure safe and effective operation of patientcare equipment and contribute to [. .. ] (e. g. , AHLTA, MHS GENESIS) and/or HP Enterprisewide database (e. g. , Smartbase) as required by DODI 6040.45 and HP program directives. Collect and report all requested data to the HP Program Manager/ Coordinator and USSOCOM HQ/ its POTFF staff. Proficiently utilize computers, software, and technologies as required for the HP program. Perform other tasks within the scope of the PT position as assigned. Required Education/ Experience/ Skills/ Training U. S. Citizenship. Secret or Top Secret Clearance, or [. .. ]
Job am 14.10.2025 bei Jobleads gefunden
Projektmitarbeiter der Geschäftsführung (m/w/d) Vollzeit in München
• München, Bayern
Führungs-/ Leitungspositionen Homeoffice möglich Abgeschlossenes Studium
Betriebliche Altersvorsorge
[. .. ] chances of interviewing at BONAGO Incentive Marketing Group by 2x Get notified about new Project Associate jobs in Munich, Bavaria, Germany. Junior Project Manager/ PMO (all genders) [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Team Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Tester for a car voice assistant project-English (Australian) speaker Junior Program Manager/ Junior Projektmanager Automotiv (all gender) Team Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Project Assistant-Clinical Safety Pharmacovigilance (office based in Munich) Supply Chain Project Coordinator (m/f/d) Product Process Support Tester for a car voice assistant project-Spanish (Spain) speaker JUNIOR PROJEKT LEITER/in (m/w/d) Event Promotion Junior Projektmanager Elektrotechnik (all gender) Working Student Smart Site Operations Strategy (m/f/d) Intern Sustainability Management (f/m/d) Working Student Medical ML Data Management (f/m/x) Project Manager-Employee Research/ Surveys Tester for a car voice assistant project-French (France) speaker Strategic Project Assistant to CSMO (m/w/d) Working Student: Product Management and Data Analyst Associate (f/m/div) Were unlocking community knowledge in a new way. Experts add insights directly [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Clinical Data Coordinator pro Jahr?
Als Clinical Data Coordinator verdient man zwischen EUR 50.000,- bis EUR 75.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Data Coordinator Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 37 offene Stellenanzeigen für Clinical Data Coordinator Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Clinical Data Coordinator Jobs?
Aktuell suchen 14 Unternehmen nach Bewerbern für Clinical Data Coordinator Jobs.
Welche Unternehmen suchen nach Bewerbern für Clinical Data Coordinator Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Clinical Data Coordinator Stellenangebote:
- Abb Vie (6 Jobs)
- IQVIA (5 Jobs)
- Georgetown University in Qatar (3 Jobs)
- Thermo Fisher Scientific (2 Jobs)
- rockITdata (1 Job)
- University of Maryland Global Campus (1 Job)
In welchen Bundesländern werden die meisten Clinical Data Coordinator Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Data Coordinator Jobs werden derzeit in Baden-Württemberg (7 Jobs), Rheinland-Pfalz (7 Jobs) und Bayern (5 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Data Coordinator Jobs?
Clinical Data Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.
