CPL Life Sciences is working with a well-established, supportive global pharmaceutical company seeking a Clinical Scientific Expert to support their Clinical Data team across all phases of clinical trials on an interim basis due to increased workload. This role is focused on clinical data review, ensuring data accuracy, scientific plausibility, and identifying trends to support decision-making and patient safety.
- 6 month contract
- Fully remote
- £18-19 per hour (PAYE)
Key Responsibilities:
- Perform in-depth patient-level clinical data review and trend analysis to ensure data quality and scientific integrity
- Support key milestones, including Interim Analyses, Database Lock, and Post-Lock activities
- Identify data discrepancies and assess clinical plausibility, escalating issues as needed
- Contribute to the development and improvement of data review strategies and processes
- Ensure adherence to study protocols and Good Clinical Practice (GCP) guidelines
- Identify and escalate subjects or data requiring medical review
- Collaborate with Pharmacovigilance teams and participate in safety monitoring meetings
- Assist in creating clinical sections of study-level and regulatory documents
- Present findings and updates at study meetings
- Use clinical data systems and tools for data collection, validation, analysis, and reporting
Requirements:
- Proven experience in clinical data review or analysis
- Scientific background
- Good understanding of clinical trial processes, GCP, and regulatory standards
- Familiarity with data management systems and reporting tools
- Excellent communication and issue-resolution skills
- Detail-oriented, with a focus on data quality and patient safety
If you have a background in clinical data analysis and scientific plausibility, apply now or send your CV to [email protected] for more information.