Data Investigator

Principal Investigator – Clinical Development (Contract) Location: Munich, Germany Employment type: Contract / Freelance ~ 12-month contract (possibility of extension) We are seeking a highly skilled and motivated Principal Investigator (PI) to join a leading clinical research organization dedicated to advancing innovative medical treatments. This role offers the opportunity to be at the forefront of clinical development, working alongside an experienced research team to deliver high-quality data and exemplary patient care. As a Principal Investigator, you will be entrusted with the conduct, oversight, and medical leadership of clinical trials at a site level. You will play a pivotal role in ensuring participant safety, maintaining compliance with Good Clinical Practice (GCP) guidelines, and driving the successful execution of studies. This position is ideal for physicians, scientists and pharmacists with a passion for clinical research who want to contribute directly to the progress of new therapies that have the potential to improve patient outcomes worldwide. Key Responsibilities: Provide overall medical leadership and direction for assigned studies, ensuring strict adherence to study protocols and regulatory requirements. Safeguard the rights, safety, and well-being of all trial participants. Evaluate participant eligibility, conduct physical assessments, and perform study-specific procedures. Review and interpret diagnostic data, including lab work, ECGs, and imaging, as required. Oversee the administration of investigational products and ensure compliance with study protocols. Maintain accurate, complete, and timely documentation of study data and source records. Act as primary liaison with sponsors, monitors, and regulatory bodies, participating in audits and inspections as required. Report adverse events promptly in compliance with study-specific and regulatory reporting requirements. Provide scientific and medical input for new study feasibility assessments. Guide and support clinical research staff to ensure quality standards are consistently met. Qualifications: M.D. or D.O. with active, unrestricted medical license in the state where research will be conducted. Board certification (or board eligibility) in a relevant specialty. Training and certification in Good Clinical Practice (GCP). Strong knowledge of clinical trial protocols, regulatory requirements, and biomedical research ethics. Excellent communication skills with the ability to collaborate cross-functionally. Demonstrated ability to critically evaluate clinical data and resolve challenges with sound judgment. Willingness to travel occasionally (up to 10%) for sponsor meetings, trainings, or professional conferences. Tangible Benefits: Competitive compensation package with performance-based incentives. Medical, dental, and vision coverage. Retirement savings plan with employer contributions. Generous paid time off and recognized company holidays. Ongoing opportunities for career development, training, and advancement within clinical research.