Study Physician sponsor dedicated in Germany

Overview

Updated: February 6, 2026
Location: DEU-Remote
Job :

Study Physician sponsor dedicated in Germany

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE

Why Syneos Health

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture unites us globally, and we take care of our people.
• We are continuously building a diverse and inclusive culture where everyone belongs.

Job Responsibilities

• Study Physician:
  Medical Doctors with fellowship/residency/specialization in Internal Medicine, Oncology, Neurology, Immuno-oncology, Cardiology, Pediatrics, Emergency Medicine, etc. preferred.
• Global Medical Monitor / Study Physician / Clinical Trial Physician for phase I–IV trials in CRO/Pharma.
• Global Project Manager / Clinical Trial Leader / Project Manager managing multiple countries in CRO/Pharma.
• Country Trial Manager / Local Project Manager / Project Manager USA in CRO/Pharma.
• Global Safety Physician / Risk Management Physician in Pharmacovigilance in CRO/Pharma.

Additional points include clinical practice experience of a minimum of 4 years; typical candidates have 10–15 years of experience post residency/fellowship; licensing may not be required depending on local legal requirements; medical monitoring and pharma company experience preferred (CRO experience acceptable). If no industry experience, alternative roles in clinical trials for a reasonable amount of time may be considered. Travel: 15–20% depending on study requirements.

Key CV keywords include clinical trial protocol writing/reviewing, identifying medically relevant data, risk mitigation and monitoring, medical quality review/clinical quality monitoring, data listing review, medical plausibility checks, patient profile review, and trial document reviews (informed consent, monitoring manuals, training plans, etc.).

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 studies across 73,000 sites and 675,000+ trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo in a highly competitive and ever-changing environment. Learn more about Syneos Health.

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company may assign other tasks at its sole discretion. Equivalency of experience, skills or education will be considered. This description complies with local laws and the EU Equality Directive for recruitment and employment. The Company is committed to compliance with the Americans with Disabilities Act, including reasonable accommodations in the application process where appropriate.

Study Physician — Medical Doctors with specified specialties; diverse pathway for global trial leadership and safety roles, with travel and industry experience considerations. We encourage diverse and inclusive candidacies and value transferable skills.