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Project Manager

vor 3 Monaten


Munich, Deutschland EPM Scientific Vollzeit

Job Title: Freelance Project Manager for Clinical Trials

Location: Germany or Remote EU

About Us: We are a privately-owned Clinical Research Organization (CRO) specializing in clinical trials. Our services encompass study design, regulatory communication, site selection and qualification, monitoring, safety management, clinical data management, statistical analysis, and study report writing. We collaborate with small to medium-sized pharmaceutical companies across Europe, North America, and Australasia, with our headquarters located in Germany.

Job Description: We are looking for a Freelance Project Manager to join our team in Germany or the EU. This role offers the chance to be a key player in a growing organization that focuses on radiology imaging and nuclear medicine. The Project Manager will oversee clinical trials, manage projects from start to finish, and serve as a primary contact for study sites and clients.

Key Responsibilities:

  • Act as the main contact for study sites and clients
  • Coordinate and manage clinical trials, ensuring projects stay on schedule and within budget.
  • Work with a multidisciplinary team to meet project goals.
  • Oversee the selection and qualification of hospital departments as trial sites.
  • Manage study-related documentation and regulatory submissions.
  • Monitor safety, data management, and statistical analysis processes.
  • Ensure compliance with relevant regulatory guidelines and standards (e.g., ICH-GCP, FDA Guidelines).
  • Handle both administrative and project management tasks as required.

Preferred Qualifications:

  • Strong communication skills and a team-oriented mindset.
  • Excellent project and time management skills.
  • Proficiency in MS Office.
  • Medical or scientific background; experience in clinical trials is a plus.
  • Willingness to take on both administrative and managerial responsibilities.

Recommended Qualifications:

  • Master’s degree (or equivalent) in natural sciences, medical/life sciences, or related fields.
  • Understanding of scientific research and clinical trial data.
  • Knowledge of clinical trial regulations and guidelines.
  • Ability to work effectively in a global setting, appreciating cultural differences.
  • Proven problem-solving abilities and the capability to simplify complex tasks.

What We Offer:

  • Flexible working hours with options for remote work.
  • Competitive hourly rates
  • A supportive international team and the opportunity to work with international clients.


If you are enthusiastic about clinical research and looking to join a dynamic team, this role offers an exciting opportunity for professional growth and development. Apply today