Site Oversight Consultant

Hobson Prior; Köln; Remote; EUR 40.000 - 60.000; Teilzeit

Zusammenfassung

A clinical research organization is seeking a Site Oversight Consultant to work remotely across Europe. The role involves approximately 15 site visits per year to ensure compliance with study protocols. Ideal candidates should have significant clinical research experience and strong knowledge of GCP. This part-time position will require travel for oversight visits and ensuring sponsor obligations are met.

Qualifikationen

• Experience in clinical research, CRA, monitor, or site management.
• Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
• Excellent communication and documentation skills.

Aufgaben

• Visit investigational sites to assess operations and compliance.
• Document findings and actions after site visits.
• Ensure documentation aligns with study protocols.

Kenntnisse

Clinical research experience

Knowledge of Good Clinical Practice (GCP)

Excellent communication skills

Jobbeschreibung

Site Oversight Consultant (Remote, Europe)

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.