Clinical Data Specialist
Posted 1 week ago by Cpl Life Sciences
£19 Per hour
Inside
Remote
United Kingdom
Summary: CPL Life Sciences is seeking a Clinical Scientific Expert/Clinical Data Expert for a 6-month remote contract with a global pharmaceutical company. The role involves supporting the Clinical Data team by reviewing clinical data for accuracy and scientific plausibility, as well as identifying trends to enhance decision-making and patient safety. This position is a response to increased workload due to ongoing research development. The role requires a strong background in clinical data review and analysis.
Key Responsibilities:
- Perform in-depth patient-level clinical data review and trend analysis to ensure data quality and scientific integrity
- Assess clinical data for scientific plausibility, highlighting any possible discrepancies in the data
- Support Interim Analyses, Database Lock, and Post-Lock activities
- Contribute to the optimisation of data review processes
- Ensure adherence to study protocols and Good Clinical Practice (GCP) guidelines
- Escalation of concerns for medical review
- Collaborate with Pharmacovigilance and Medical Information teams when required
- Present findings and updates at study meetings
- Use clinical data systems and tools for data collection, validation, analysis, and reporting
Key Skills:
- Proven experience in clinical data review or analysis
- Scientific background
- An understanding of clinical trial processes, GCP, and regulatory standards
- Experience with data management systems and reporting tools
- Excellent communication and issue-resolution skills
Salary (Rate): £19.00/hr
City: undetermined
Country: United Kingdom
Working Arrangements: remote
IR35 Status: inside IR35
Seniority Level: undetermined
Industry: Other
CPL Life Sciences are working with a well-established, innovative global pharmaceutical company seeking a Clinical Scientific Expert/ Clinical Data Expert to support their Clinical Data team across all phases of clinical trials on an interim basis. The role is required due to increased workload within the team, with new research in on-going development. 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
- Assess clinical data for scientific plausibility, highlighting any possible discrepancies in the date
- Support Interim Analyses, Database Lock, and Post-Lock activities
- Contribute to the optimisation of data review processes
- Ensure adherence to study protocols and Good Clinical Practice (GCP) guidelines
- Escalation of concerns for medical review
- Collaborate with Pharmacovigilance and Medical Information teams when required
- 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
- An understanding of clinical trial processes, GCP, and regulatory standards
- Experience with data management systems and reporting tools
- Excellent communication and issue-resolution