Clinical Project Associate
4 weeks ago
25 GBP - 25 GBP
- Uxbridge, United Kingdom
- Contract
**Freelance Clinical Trial Associate Opportunity with Leading Global Pharma - UK Based**
**Company Overview**: Join a dynamic and innovative global pharmaceutical company committed to advancing healthcare through groundbreaking research and development. We are seeking a highly motivated and experienced Freelance Clinical Trial Associate to contribute to our cutting-edge clinical trials.
- **Position: Freelance Clinical Trial Associate**
**Location: West London - hybrid (3 days per week)**
**Responsibilities**:
- Collaborate with cross-functional teams to support the planning, execution, and closure of clinical trials.
- Assist in the preparation and maintenance of essential trial documentation, ensuring compliance with regulatory standards and company procedures.
- Coordinate with investigative sites, vendors, and study personnel to facilitate smooth trial operations.
- Conduct site qualification, initiation, monitoring, and close-out visits as needed.
- Ensure timely collection and review of study data, resolving data discrepancies and issues as they arise.
- Support the preparation of regulatory submissions and responses to health authorities.
- Strong with Word, PowerPoint, and Excel. Knowledge of FDA and or EMEA Regulations, ICH Guidelines, GCPs, and/or familiarity with standard clinical operating procedures is a plus.
**Qualifications**:
- Bachelor's degree in a relevant scientific discipline.
- Proven experience as a Clinical Trial Associate in the pharmaceutical industry.
- Strong understanding of GCP, ICH guidelines, and regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to work independently and collaboratively in a fast-paced environment.
- Proficient in the use of clinical trial management systems and other relevant software.
**Duration**:
- 12 months
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