Local Clinical Trial Manager – Single Sponsor

This is a fully remote position, open to applicants in Germany.

📋 Description

• Accountable for overseeing site management, clinical monitoring, and central monitoring deliverables with an emphasis on patient safety, adherence to protocols/GCP/regulatory standards, and ensuring data integrity.

• Manages site interactions from the time of activation through to site closure.

• This includes tasks such as patient recruitment, facilitating investigator payments, and other associated activities.

• Alerts the project manager to any risks that may impact clinical trial management deliverables (including timeline, quality, and budget) as well as any activities and requests that exceed the contracted scope.

• Works in collaboration with other functional leaders like Study Start Up, Patient Recruitment, and Data Management to ensure smooth delivery handovers and achieve anticipated study milestones such as site activation goals, enrollment objectives, and database lock timelines.

⛳️ Requirements

• Bachelor’s degree or RN in a relevant field or a suitable combination of education, training, and experience.

• Proven ability to lead and align teams towards achieving project milestones.

• A minimum of 4-6 years of experience in the pharmaceutical industry or clinical research.

• Ideally, 2-3 years of monitoring experience along with trial management experience.

• Proven capability to operate effectively in an international setting.

• Demonstrated expertise in site management and monitoring (clinical or central).

• Experience with risk-based monitoring is preferred.

• Solid understanding of clinical trial management financial principles and budget oversight.

• Familiarity with Good Clinical Practice/ICH Guidelines and other relevant regulatory requirements.

• Must exhibit strong computer skills.

• Experience with start-up activities is preferred.

• Experience in Neurology, Immuno-Inflammation (Respiratory/Dermatology), Rare Diseases, and/or Vaccines is desired.

• Proficient in both English and German.

• Proven ability to apply problem-solving techniques to address complex issues, and a risk management approach to identify and mitigate potential challenges in the successful execution of a clinical research project.

• Moderate travel may be necessary, approximately 25%.

🏝️ Benefits

• We are dedicated to fostering the growth of our employees through career development and advancement; providing supportive and engaged line management; offering technical and therapeutic area training; recognizing peer contributions; and implementing a total rewards program.

• We are committed to cultivating an inclusive culture where you can genuinely be yourself.