Freelance Clinical Oversight Monitor - Switzerland & Italy

Proclinical are seeking for a talented and experienced Clinical Oversight Monitor to join a global, mid-sized pharmaceutical organisation specialised in Rare Diseases. The successful candidate will be responsible for ensuring data accuracy and integrity during clinical trials and will be responsible for monitoring in accordance with all applicable regulations.

Responsibilities

• Monitor clinical studies to ensure compliance with applicable regulations and standards.
• Perform co-monitoring quality-led, on-site visits with the assigned monitoring team.
• Provide support to CRAs and investigational site personnel to ensure data integrity is maintained during all facets of the study maintenance.
• Develop and maintain relationships with key stakeholders including CRO, principal investigators, and other external parties.
• Undertake motivational calls to support patient recruitment boosting activity.
• Analyse data from clinical trials and ensure accuracy and integrity.
• Provide guidance and support to study teams as needed.

Requirements

• Bachelor's Degree in a scientific discipline (e.g. biology, chemistry).
• 5+ years of experience in clinical research.
• 9+ years of experience in site management and on-site monitoring (CRA experience).
• Strong understanding of Good Clinical Practices (GCP) and the EMA.
• Excellent interpersonal, communication, and problem-solving skills.
• Ability to work independently and as part of a team.
• Ability to multi-task and manage multiple projects.
• Proficiency in MS Office Suite.
• Willing to travel regionally up to 40%.

If you are having difficulty in applying or if you have any questions, please contact Roy Nelson at +44 203 148 8373.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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