Clinical Research Physician — Lead Patient Safety Oversight

ICON; Groningen; Vor Ort; EUR 80.000 - 110.000; Vollzeit

Benefits dieser Stelle

Annual leave entitlements

Health insurance offerings

Retirement planning options

LifeWorks EAP

Life assurance

Childcare vouchers

Zusammenfassung

ICON is a global healthcare intelligence and clinical research organisation driving faster access to medicines. We seek a qualified Keuringsarts/Physician Assistant to screen participants, monitor safety, and contribute to cutting-edge clinical studies.

The role focuses on safeguarding participant welfare, supporting site operations, and advancing research with a strong emphasis on independence and collaborative ethics. Dutch and English communication are essential.

Qualifikationen

• Work experience in a clinical setting as physician or PA or recently graduated in these roles.
• BIG registration is required for physicians and PAs; candidates without registration cannot be considered.
• Strong clinical assessment skills and a professional focus on patient safety and ethical research practices.
• Interest in and/or experience with clinical drug trials is a plus.
• Ability to work independently within a multidisciplinary team and contribute to study quality.

Aufgaben

• Screen healthy participants and patients for clinical studies.
• Provide medical support during study procedures.
• Ensure safety and well‑being of participants during trials.
• Contribute medically by reviewing study protocols and collaborating with the Site Study Team.
• Maintain the level of clinical expertise required for practice and research.

Kenntnisse

Clinical assessment skills

Patient safety focus

Team collaboration

Dutch and English communication

Ausbildung

BIG registration (Netherlands)

Jobbeschreibung

ICON is a global healthcare intelligence and clinical research organisation driving faster access to medicines. We seek a qualified Keuringsarts/Physician Assistant to screen participants, monitor safety, and contribute to cutting-edge clinical studies.

The role focuses on safeguarding participant welfare, supporting site operations, and advancing research with a strong emphasis on independence and collaborative ethics. Dutch and English communication are essential.