Site Oversight Consultant

Hobson Prior; Deutschland; Remote; EUR 60.000 - 80.000; Teilzeit

Zusammenfassung

A leading life sciences recruitment agency is seeking a Site Oversight Consultant to support clinical research activities remotely from anywhere in Europe. This part-time role involves conducting oversight visits at investigational sites, ensuring compliance with protocols and reporting any risks. The ideal candidate will have experience in clinical research and knowledge of Good Clinical Practice. The position may require international travel for site visits.

Qualifikationen

• Experience in roles like Clinical Research Associate (CRA), monitor, or site management.
• Strong knowledge of ICH guidelines and regulatory requirements.
• Familiarity with sponsor oversight responsibilities.

Aufgaben

• Conduct oversight visits at investigational sites worldwide.
• Document findings and actions after site visits.
• Review site documentation and processes for compliance.
• Report compliance risks or deviations.
• Collaborate with internal teams for follow-up actions.
• Maintain auditable records of oversight activities.

Kenntnisse

Experience in clinical research

Knowledge of Good Clinical Practice (GCP)

Excellent communication skills

Strong documentation skills

Willingness to travel internationally

Jobbeschreibung

Hobson Prior is seeking a Site Oversight Consultant to support clinical research activities remotely from anywhere in Europe, with occasional travel. This part‑time role involves conducting oversight visits at investigational sites worldwide, ensuring compliance with study protocols and regulatory requirements. You will play a key role in maintaining sponsor oversight obligations and contributing to inspection readiness.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities

• Visit investigational sites (approximately 15 visits per year, each lasting 3-5 days) to assess operations and compliance.
• Use provided templates to document findings and actions after site visits.
• Review site documentation and processes to ensure they align with study protocols and standard procedures.
• Identify and report any compliance risks or deviations observed during visits.
• Collaborate with internal teams to ensure follow‑up actions are completed.
• Maintain clear and auditable records of all oversight activities.

Key Skills and Requirements

• Experience in clinical research, particularly in roles like Clinical Research Associate (CRA), monitor, or site management.
• Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements.
• Familiarity with sponsor oversight responsibilities and documentation standards.
• Excellent communication and documentation skills.
• Willingness to travel internationally for site visits as needed.

For more information, please contact Terrah‑Leigh Pietersen.

If you are interested in applying to this exciting opportunity, click “Apply” or to speak to one of our specialists visit the “Contact Us” page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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