Site Oversight Consultant

R&D Partners; Essen; Remote; EUR 60.000 - 80.000; Teilzeit

Zusammenfassung

A leading life sciences recruiter is seeking a Site Oversight Consultant to support clinical research activities. This part-time remote role requires conducting oversight visits at investigational sites worldwide, ensuring compliance with study protocols and regulatory requirements. Ideal candidates will have clinical research experience, strong knowledge of GCP, and completion of approximately 15 site visits per year.

Qualifikationen

• Experience in roles like Clinical Research Associate (CRA), monitor, or site management.
• Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
• Excellent communication and documentation skills.

Aufgaben

• Visit investigational sites approximately 15 times per year for compliance.
• Document findings and actions after site visits.
• Collaborate with internal teams to ensure follow-up actions.

Kenntnisse

Experience in clinical research

Strong knowledge of Good Clinical Practice (GCP)

Excellent communication skills

Familiarity with ICH guidelines

Willingness to travel internationally

Jobbeschreibung

R&D Partners 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, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

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

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