Clinical Project Manager

Carrot Recruitment; Leipzig; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

A leading medical technology company is seeking a Clinical Project Manager in Germany. The role involves managing clinical studies, ensuring compliance with regulations, and overseeing budgets. Ideal candidates will have a strong background in clinical research and oncology, with experience in medical device studies.

Qualifikationen

• Proven experience in Clinical Research and managing complex studies in Europe.
• Extensive experience in Oncology and/or radiation therapy.

Aufgaben

• Plan, manage, and execute clinical studies from concept through completion.
• Oversee study budgets, timelines, and resource allocation.
• Lead interactions with investigational sites and regulatory authorities.

Kenntnisse

Clinical Research

Project Management

Oncology

Regulatory Compliance

GCP

Ausbildung

BSc / MSc / PhD in Life Sciences

Tools

Veeva Vault Clinical Suite

Jobbeschreibung

Clinical Project Manager – Germany – Medical Devices

The Company

Carrot is partnering with a Global medical technology company focused on manufacturing medical devices, instrument systems and reagents. They are now looking for a Clinical Project Manager based in Germany but may also consider applicants from France, Ireland and the Netherlands. You will participate in cross functional teams working across clinical studies from initial set up to study completion ensuring successful planning and execution.

The Role

• Plan, manage, and execute clinical studies from concept through completion.
• Ensure compliance with GCP, industry regulations, and company global clinical procedures.
• Oversee study budgets, timelines, and resource allocation.
• Develop and manage essential clinical documents, including Clinical Investigation Plans, Informed Consent Forms, and Study Management Plans.
• Lead interactions with investigational sites, vendors, key opinion leaders (KOLs), and regulatory authorities.
• Monitor study progress and provide regular updates to Clinical Affairs leadership.
• Conduct site management, clinical product management, and field support activities as needed.
• Support internal and external audits, ensuring resolution of findings.
• BSc / MSc / PhD in Life Sciences, Biomedical Engineering, Medicine or similar background
• Proven experience in Clinical Research and managing complex studies in Europe
• Extensive experience in Oncology (Radioembolization preferable) and / or experience in radiation therapy pharma / device
• Experience with medical device studies (strongly preferred)
• Prior experience with Veeva Vault Clinical Suite (CTMS, CDMS and eTMF)
• Strong knowledge of clinical trial regulations, GCP, and industry best practices.

What should you do next?

This Clinical Project Manager role is one not to be missed; it encompasses the opportunity to work with a well-known Medical Technology company.

To discuss this role further or to find out about other roles I’m currently working on, please get in touch or hit apply to submit your current CV.

Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.

Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and / or expression.

If there are any arrangements or adjustments we can make to assist you at interview then please let us know and we'll be more than happy to assist.