10,296 clinical study manager remote-Jobs in ganz Deutschland.

Beliebte Städte

Top 5

Berlin11746 Hamburg6018 Muenchen5630 Franckfurt3073 Stuttgart2846

Alle Standorte anzeigen

Stellenangebote werden angezeigt

Subject Well Inc.

Freelance Study Coordinator (Oncology / Clinical Trials)

Vor 8 Tagen

Remote
Vertrag

... boundaries and patient autonomy. Benefits - Remote freelance opportunity. - Competitive project-based compensation. - Meaningful work supporting cancer patients and clinical research. - Exposure to innovative oncology clinical trials. Interested? If you are a medical professional with oncology or clinical research experience and ...

Deutschland

IQVIA

Clinical Interview Rater (CIR) - German Speaking

Vor 1 Tag

Remote

Clinical Interview Rater (CIR) – German Speaking Study: M26-298 Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Interview Rater (CIR) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We ...

Hamburg, Deutschland

IQVIA

Clinical Interview Rater (CIR) - German Speaking

Vor 5 Tagen

Remote
Teilzeit

Heidelberg, Deutschland

Astrum

Clinical Research Associate - Central or East regions Germany

Vor 12 Tagen

Remote
Hybrid
Vor Ort

Project Management
Biomedicine

... Associate to plan, execute and monitor clinical trials from site initiation through close-out. You will ensure compliance with regulatory requirements, ICH-GCP and study protocols, while prioritising patient safety, data integrity and timelines. As the primary link between the Project Manager, study sites and sponsor, you will ...

Muenchen, Deutschland

Thermo Fisher Scientific

Assistant CRA - FSP (m/f/d)

Vor 12 Tagen

Remote
Vertrag

... seeks an Assistant CRA for a 2-year fixed-term remote contract to support clinical trial site management and monitoring across global studies. The role involves remote data review, site communication, protocol compliance assessment, and regulatory documentation under ICH GCP guidelines. Responsibilities - Conduct remote site ...

Deutschland

Indero

Project Manager II, Early Phase (Germany)

Vor 11 Tagen

Vertrag

Project Management

... monitoring, controlling and closure of assigned clinical trials. The Project Manager II, EPTR oversees and coordinates study resources to ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs), good clinical practices, regulatory and study-specific ...

Deutschland

AstraZeneca

Clinical Research Associate (CRA) (m/w/d) - Zelltherapie

Vor 2 Tagen

Remote

Biomedicine

AstraZeneca seeks a Clinical Research Associate to monitor cell therapy trials in Hamburg, Germany. The role involves overseeing study data integrity, site management, recruitment tracking, and regulatory compliance across all trial phases. Responsibilities - Monitor cell therapy clinical studies and ensure accurate, complete, ...

Hamburg, Deutschland

Assistant CRA - FSP (m/f/d)

Vor 3 Tagen

Remote
Vollzeit
Vertrag

... monitoring activities on assigned project(s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and company procedural documents by reviewing study data from various sources remotely. You will contact study sites to collect study documentation, resolve issues and request outstanding information. What you'll ...

Deutschland

Indero

Project Manager (Germany)

Vor 11 Tagen

Vertrag

Project Management

... initiation, planning, execution, monitoring, controlling and closure of assigned clinical research projects. The Project Manager I must ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs), good clinical practices, regulatory and study-specific ...

Deutschland

TFS HealthScience

Senior Clinical Research Associate (m/f/d)

Vor 2 Tagen

Remote
Hybrid
Vor Ort
Vertrag

Project Management
Biomedicine

... accurate site level information - Participate in audit and/or inspection, it’s preparation and follow-up activities, as needed. - Order, ship, and reconcile clinical investigative supplies for study sites, if applicable. - May assist the Clinical Research Manager or Project Manager in certain aspects of project activities ...

Hamburg, Deutschland

AstraZeneca

Local Study Associate Director (LSAD) / Clinical Project Lead (m/w/d)

Vor 12 Tagen

Vor Ort
Vollzeit

... Teamarbeit und kompetente Spezialist:innen gleichermaßen ankommt. Wenn Sie jetzt denken " Hier ist meine Zukunft! ", dann freuen wir uns auf Ihre Bewerbung als Local Study Associate Director (LSAD) / Clinical Project Lead (m/w/d), Office-based. Finden auch Sie einen Arbeitsplatz mit hervorragenden Perspektiven, bei dem Sie Ihr ...

Hamburg, Deutschland

TFS HealthScience

Clinical Research Associate (m/f/d)

Vor 12 Tagen

Remote
Hybrid
Vor Ort
Vertrag

Biomedicine

... their goals. The Clinical Research Associate will function operationally as a member of a Project Team and is responsible for the initiation, on–site and/or remote monitoring, close outof study sites during study conduct, according to company policies, SOPs and GCP and ICH guidelines and other regulatory requirements. Key ...

Cassel, Deutschland

PSI CRO

Clinical Research Associate I (CRA)

Vor 2 Tagen

Remote
Hybrid
Vor Ort
Vollzeit
Vertrag

Biomedicine

... with study protocols and regulatory requirements - Be responsible for site communication and management - Build effective relationships with investigators and study teams - Be involved in site identification process Qualifications - Completed advanced CRA/Clinical Monitoring training (e.g., mibeg, Pharmaakademie, or comparable) ...

Muenchen, Deutschland

LabConnect

Project Manager -Germany (Remote)

Vor 3 Tagen

Remote
Vollzeit
Vertrag

Project Management

... manager to ensure data is delivered on time per the SOW. - Review and analyze operational, quality, and performance related metrics to assess the success of study oversight activities. - Liaise with managers/supervisors in other departments to stay informed of operational changes. - Collaborate with project managers in ...

Köln, Deutschland

Vivalyx GmbH

Senior Clinical Research Associate (CRA II) (m/f/d)

Vor 12 Tagen

Remote
Hybrid
Vor Ort
Vertrag

Biomedicine

... Act as Vivalyx’s primary operational contact for investigators and study coordinators. - Prepare, conduct, and document site initiation, interim on-site and remote monitoring, and closeout visits. - Perform source data review and verification. - Track study progress enrollment, follow-up visits, data-entry status, queries, ...

Köln, Deutschland

IQVIA

(Senior) Clinical Trial Lead (m/w/d)

Vor 3 Tagen

Vollzeit

... Healthy Volunteer clinical trials, with demonstrated end-to-end accountability. - Essential: Early phase study-design expertise: In-depth knowledge of early phase study designs, protocol writing and clinical pharmacology. Experience should include several relevant study types, such as first-in-human, single- or multiple-ascending-dose, ...

Franckfurt, Deutschland

Edwards Lifesciences

Clinical Research Associate / Senior CRA

Vor 12 Tagen

Biomedicine

... adherence to study protocol at assigned clinical sites. This role will be to work on medical device trials in Cardiology. How you will make an impact: - Conducting Clinical Monitoring activities at sites across Germany - Serve as key contact to assigned clinical sites throughout the study process - Is accountable for achieving ...

Hamburg, Deutschland

IQVIA

Trainee Clinical Research Associate (m/w/d), Home-Office in Germany

Vor 12 Tagen

Remote
Vollzeit
Vertrag

Biomedicine

... - Complete therapeutic area, protocol-specific, and clinical research training required to perform assigned responsibilities. - Gain practical experience in study conduct and site management through collaboration with experienced clinical research professionals. - Conduct site qualification, initiation, monitoring, and ...

Franckfurt, Deutschland

Astrum

Senior Biostatistician

Vor 3 Tagen

... calculations - Randomization strategies - Estimand definitions - Author Statistical Analysis Plans (SAPs) and review tables, figures, and listings (TFLs). - Review Clinical Study Protocols (CSPs) and Clinical Study Reports (CSRs). - Review and approve programming specifications, statistical outputs, and analysis datasets prepared ...

Muenchen, Deutschland

ICON

CRA II FSP AZ program

Vor 2 Tagen

Biomedicine

... staff to facilitate study conduct - Perform data review and resolve queries to maintain high-quality clinical data - Contribute to preparation and review of study documentation and reports Requirements - Bachelor's degree in scientific or healthcare-related field - Minimum 2 years of Clinical Research Associate experience ...

Mannheim, Deutschland