Freelance Clinical Oversight Monitor

Vor 5 Tagen

Lugano, Schweiz Proclinical Vollzeit

**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%.

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.

LI-RN1

Clinical

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