Clinical Data Coordinator Stellenangebote


+ Suchfilter (0 aktiv)

27 Jobs für Clinical Data Coordinator


Stellenangebote Clinical Data Coordinator Jobs


Neu Job vor 4 Std. bei Jobware gefunden TRB Chemedica AG

Produktmanager Healthcare (m/w/d) Marketing

• Feldkirchen bei München Homeoffice möglich 30+ Urlaubstage [. .. ] (m/w/d) Digital Marketing Manager Healthcare (m/w/d) Marketing Communications Manager Healthcare (m/w/d) Content Manager Healthcare/ Pharma (m/w/d) Commercial Product Specialist (m/w/d) Clinical Product Manager (m/w/d) Medical Affairs Manager [...]
MEHR INFOS ZUM STELLENANGEBOT[...] (m/w/d) Scientific Product Specialist (m/w/d) Medical Science Liaison (m/w/d) (mit leichter Marketingnähe) Medical Content Specialist (m/w/d) Event Congress Manager Healthcare (m/w/d) Healthcare Communications Manager (m/w/d) Education Training Manager Medical Devices [. .. ] Manager Healthcare UX Content Manager Med Tech Healthcare E-Commerce Manager Digital Communications Manager Pharma Marketing Automation Specialist Healthcare Scientific Affairs Specialist Clinical Research Associate (mit Produktfokus) Medical Information Specialist Evidence Data Manager Healthcare Clinical Evidence Manager Med Tech Regulatory Product Communication Specialist Medical Event Manager Healthcare Training Coordinator Medical Congress Coordinator Education Specialist Medical Devices Health Communications Specialist Corporate Communications Manager Healthcare 71621652 [. .. ]

▶ Zur Stellenanzeige
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 [. .. ]

▶ Zur Stellenanzeige
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 [. .. ]

▶ Zur Stellenanzeige
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 accelerate [...]
MEHR INFOS ZUM STELLENANGEBOT[...] the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all [. .. ] 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 [. .. ] 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 with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]

▶ Zur Stellenanzeige
Job am 14.10.2025 bei Jobleads gefunden

Head of Scientific Platforms and Core Facilities (80-100)

• Allschwil, Basel- Landschaft Führungs-/ Leitungspositionen [. .. ] facilities such as BSL 1, 2 and 3 lab infrastructure (including teaching lab) , vector lab, central lab and animal facilities, imaging and sequencing and biobanks Knowledge [...]
MEHR INFOS ZUM STELLENANGEBOT[...] hubs such as data analytics, datamanagement, Research IT, bioinformatics, health social sciences and projects and grantssupport Set departmental goals, steer key initiatives and allocate resources to build a strong, purpose-driven service portfolio that supports research excellence across the institute Advance scientific methodologies and drive innovation by integrating new technologies (e. g. AI, remote [. .. ] of Department In their native language, Swiss TPH employees talk about what motivates them in their daily work. Scientific Project Leader Sonia Borrell, Scientific Project Leader Study Nurse Main Secretary Coordinator Saskia Strasser, Main Secretary Coordinator Ph D Student Scientific Collaborator Clinical Consultant How to apply: Please submit your application online. CV Motivational letter including names and contact information (email or phone number) of 1 2 references Reference letters and diploma Swiss TPH is committed to fostering an inclusive and diverse workplace that values and respects differences across gender, race, ethnicity, disability, [. .. ]

▶ Zur Stellenanzeige
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 [. .. ]

▶ Zur Stellenanzeige
Button Jobabo Nichts verpassen: Jobs per eMail
► Speichern Sie jetzt Ihre Jobsuche!

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 [. .. ] 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 [. .. ] 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 with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]

▶ Zur Stellenanzeige
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 [...]
MEHR INFOS ZUM STELLENANGEBOT[...] biotechnology, 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 [. .. ] 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 with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]

▶ Zur Stellenanzeige
Job am 28.08.2025 bei Jobleads gefunden

Projektmitarbeiter der Geschäftsführung (all genders) Vollzeit in München

• München, Bayern Führungs-/ Leitungspositionen Homeoffice möglich Abgeschlossenes Studium [. .. ] Get notified about new Project Associate jobs in Munich, Bavaria, Germany. Junior Project Manager/ PMO (all genders) Tester for a car voice assistant project-English (Australian) speaker Team [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Assistant Project Coordinator (m/f/x) Corporate Communications Europe Team Supply Chain Project Coordinator (m/f/d) Product Process Support Greater Munich Metropolitan Area 4 weeks ago Project Assistant-Clinical Safety Pharmacovigilance (office based in Munich) Junior Program Manager/ Junior Projektmanager Automotiv (all gender) Hallbergmoos, Bavaria, Germany 1 month ago Client Success Project Business Coordinator (m/f/x) Tester for a car voice assistant project-Spanish (Spain) speaker JUNIOR PROJEKT LEITER/in (m/w/d) Event Promotion Working Student Smart Site Operations Strategy (m/f/d) Junior Projektmanager Elektrotechnik (all gender) Project Manager-Employee Research/ Surveys Working Student: Product Management and Data Analyst Associate (f/m/div) Tester for a car voice assistant project-French (France) speaker Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 60156860 [. .. ]

▶ Zur Stellenanzeige
Job am 03.07.2025 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 [. .. ]

▶ Zur Stellenanzeige
Job am 01.07.2025 bei Jobleads gefunden

Clinical Trial Site Relationship Coordinator

• München, Bayern Clinical Trial Site Relationship Coordinator Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Operations team in Munich. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our [. .. ] Coordinator Sponsor Dedicated Clinical Trial Assistant in Munich area Senior Clinical Research Associates (experienced) - Germany (Senior) Research Manager-Spine Neurosurgery Expert Clinical Trials Statistics and Programming Working Student-Clinical Data Processing (m/f/d) Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr 53524867 [. .. ]

▶ Zur Stellenanzeige
Neu Job vor 4 Std. bei Neuvoo gefunden Sanofi Clinical Operations Study Country Lead I-all genders • Frankfurt, Hessen Führungs-/ Leitungspositionen Clinical Operations Study Country Lead I (COSCL) - all genders Join the engine of Sanofis mission where deep immunoscience meets bold, AI-powered research. In the Clinical Study Unit, youll [...]
MEHR INFOS ZUM STELLENANGEBOT[...] drive breakthroughs that could turn the impossible into possible for millions. About Sanofi: Were an R D-driven, AI-powered biopharma [. .. ] drive quality and study KPIs Coordinate with Medical Advisors, Site Engagement Leads, and other key stakeholders Establish productive partnerships with Medical Affairs for trial conduct activities Quality Compliance Assurance Ensure data quality, patient safety, and compliance with study metrics Oversee appropriate data collection and query resolution processes Collaborate on audit and inspection activities Maintain system readiness (PAI, TMF, CTMS) and ensure CRA training compliance Required Qualifications and Experience: Bachelors or Masters degree (or higher) in medicine, pharmacy, biology, biochemistry, or related natural science Mandatory: Clinical Research experience Preferred: Project management experience combined with field monitor or site-coordinator background Solid knowledge of clinical development processes and relevant therapeutic areas Core Competencies: Strong project management skills with proven ability to manage complex timelines Excellent problem-solving and risk-management capabilities in clinical study environments Proficiency in data analytics and digital tools, platforms, and systems Change management skills with adaptability [. .. ]

▶ Zur Stellenanzeige
Neu Job vor 4 Std. bei Neuvoo gefunden Sanofi

Clinical Operations Study Country Lead I-all genders

• Berlin Führungs-/ Leitungspositionen Clinical Operations Study Country Lead I (COSCL) - all genders Join the engine of Sanofis mission where deep immunoscience meets bold, AI-powered research. In the Clinical Study Unit, youll [...]
MEHR INFOS ZUM STELLENANGEBOT[...] drive breakthroughs that could turn the impossible into possible for millions. About Sanofi: Were an R D-driven, AI-powered biopharma [. .. ] drive quality and study KPIs Coordinate with Medical Advisors, Site Engagement Leads, and other key stakeholders Establish productive partnerships with Medical Affairs for trial conduct activities Quality Compliance Assurance Ensure data quality, patient safety, and compliance with study metrics Oversee appropriate data collection and query resolution processes Collaborate on audit and inspection activities Maintain system readiness (PAI, TMF, CTMS) and ensure CRA training compliance Required Qualifications and Experience: Bachelors or Masters degree (or higher) in medicine, pharmacy, biology, biochemistry, or related natural science Mandatory: Clinical Research experience Preferred: Project management experience combined with field monitor or site-coordinator background Solid knowledge of clinical development processes and relevant therapeutic areas Core Competencies: Strong project management skills with proven ability to manage complex timelines Excellent problem-solving and risk-management capabilities in clinical study environments Proficiency in data analytics and digital tools, platforms, and systems Change management skills with adaptability [. .. ]

▶ Zur Stellenanzeige
Job gestern bei Neuvoo gefunden Georgetown University in Qatar Clinical Research Coordinator I • Ingelheim am Rhein, Rhineland- Palatinate Work-Life-Balance [. .. ] close-knit group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world. Requirements Job [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Overview The Clinical Research Coordinator serves as clinical research coordinator for phase I, II, and III oncology clinical trials conducted in the Clinical Research Management Office (CRMO) of Lombardi Comprehensive Cancer Center. Incumbent duties include, but are not limited to: Responsible for overall coordination of assigned clinical trials throughout the trial lifecycle. Interface with study [. .. ] appropriate staff on assigned clinical trials. Regularly update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials. Collaborate with Data Manager (s) to assure documentation for the clinical trial is complete and accurate; assist with query resolution in a timely manner. Schedule/ facilitate sponsor meetings including PSV, SIV, MV Document and report serious adverse events per protocol and institutional policy, with input from PI or senior member of clinical research [. .. ]

▶ Zur Stellenanzeige
Job vor 2 Tagen bei Neuvoo.com gefunden R D Partners

Clinical Research Coordinator/ / Essen, Germany

• Essen Advance oncology research at the frontline-freelance CRC needed in Essen to support Multiple Myeloma studies. R D Partners is seeking a Clinical Research Coordinator to join a hospital [...]
MEHR INFOS ZUM STELLENANGEBOT[...] site in Essen, Germany, on a freelancing basis. This role focuses on supporting oncology studies, specifically in the area of Multiple Myeloma. Please note that to be considered for this role you must have the right to work in this location. Responsibilities: Perform data entry and resolve queries in the e CRF system (Inform) . Provide support for oncology studies with a focus on Multiple Myeloma. Key Skills and Requirements: Experience with data entry and query resolution in oncology studies. Proficiency in using the e CRF Inform system. Native German language skills are required. Experience with [. .. ]

▶ Zur Stellenanzeige
Job vor 5 Tagen bei Neuvoo gefunden GULP experts united Employee as study coordinator (m/f/d) • Hamburg [. .. ] being taken on by our business partners Tailored further training opportunities and free language courses A wide range of employee benefits Your tasks Management of the Teamcenter [...]
MEHR INFOS ZUM STELLENANGEBOT[...] software for study data and documentation Booking test rooms and scheduling test subjects Procurement and provision of study materials and equipment Carrying out the studies: Application of products to subjects skin according to study requirements Carrying out measurements and other tests to evaluate the skin care products Ensuring compliance with safety and ethical guidelines [. .. ] the antiperspirant effect under warm conditions Your profile Completed training or studies in the field of natural sciences, cosmetic sciences or a related field Experience in conducting volunteer studies or clinical trials, ideally in the field of skin care or cosmetics Good knowledge in the use of database software and Microsoft Office applications Willingness to be present during ongoing studies Very good written and spoken German and English skills Careful way of working and attention to detail Team and communication skills [. .. ]

▶ Zur Stellenanzeige
Job vor 8 Tagen bei Neuvoo gefunden AMBOSS

Marketing Engagement Coordinator (US Clinicians)

• Berlin [. .. ] are AMBOSS and we are looking for a Marketing Sales Representative to join our team, and shape the future of medical education with us About AMBOSSAMBOSS is [...]
MEHR INFOS ZUM STELLENANGEBOT[...] a dynamic learning and clinical decision support tool committed to empowering physicians globally to deliver optimal care. Since our inception in, weve harnessed cutting-edge technology to transform the way physicians acquire and apply scientific knowledge. Each AMBOS Sian is passionate about being the champion of clinicians today-this motivates and unites us each day [. .. ] platform. Assist in managing residency program group discounts, including communicating with interested residents, tracking participation, and ensuring timely delivery of materials or follow-ups. Collaborate with cross-functional teamsincluding Marketing, Data Analytics, Customer Support, and the U. S. Students Commercial teamto align outreach efforts and share learnings. Analyze engagement data and user feedback to evaluate the success of initiatives and identify opportunities to improve future events and campaigns. Contribute to new outreach experiments, bringing creativity and initiative to test new formats, [. .. ]

▶ Zur Stellenanzeige
Job vor 11 Tagen bei Neuvoo.com gefunden R D Partners Clinical Research Coordinator/ / Aachen, Germany • Aachen Join us as a Clinical Research Coordinator in Aachen and help shape the future of clinical development-freelance flexibility, hospital-based impact. R D Partners is seeking a Clinical Research [...]
MEHR INFOS ZUM STELLENANGEBOT[...] Coordinator to join a hospital site in Germany, on a freelancing basis. This role offers an exciting opportunity to contribute to clinical development within a CRO environment. [. .. ] Employment Agency in relation to this vacancy. By submitting this application, you confirm that youve read and understood our privacy policy, which informs you how we process and safeguard your data-https:/ / 70417157 [. .. ]

▶ Zur Stellenanzeige
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 [. .. ] 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 [. .. ] 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 with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]

▶ Zur Stellenanzeige
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 [. .. ] 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 [. .. ] 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 with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]

▶ Zur Stellenanzeige
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 [. .. ] 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 [. .. ] 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 with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]

▶ Zur Stellenanzeige
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 [. .. ] 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 [. .. ] 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 with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]

▶ Zur Stellenanzeige
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 [. .. ] 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 [. .. ] 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 with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]

▶ Zur Stellenanzeige
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 [. .. ] 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 [. .. ] 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 with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]

▶ Zur Stellenanzeige
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 [. .. ] 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 [. .. ] 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 with a risk-based monitoring approach (including centralized data review) through our integrated Clinical [. .. ]

▶ Zur Stellenanzeige
Jobs


1 von 2Weiter »   Weitere Suchergebnisse laden »  

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 27 offene Stellenanzeigen für Clinical Data Coordinator Jobs.


Wieviele Unternehmen suchen nach Bewerbern für Clinical Data Coordinator Jobs?

Aktuell suchen 8 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:


  • Medpace (8 Jobs)
  • TRB Chemedica AG (2 Jobs)
  • Sanofi (2 Jobs)
  • R D Partners (2 Jobs)
  • Georgetown University in Qatar (1 Job)
  • GULP experts united (1 Job)


In welchen Bundesländern werden die meisten Clinical Data Coordinator Jobs angeboten?

Die meisten Stellenanzeigen für Clinical Data Coordinator Jobs werden derzeit in Nordrhein-Westfalen (5 Jobs), Bayern (3 Jobs) und Niedersachsen (3 Jobs) angeboten.


Zu welchem Berufsfeld gehören Clinical Data Coordinator Jobs?

Clinical Data Coordinator Jobs gehören zum Berufsfeld Sozial- und Gesundheitswesen.


Jobs per Email


Verpassen Sie keine Jobs!
Wir informieren Sie kostenfrei über neue Jobangebote!


Datenschutzklärung lesen


Dauer: 0.049 s., Vers. V.2025-d-2007-Ind-141