CPL Life Sciences are actively hiring in collaboration with a market-leading global pharmaceutical company, seeking a Clinical Project Associate to provide operational and program-level support for clinical trials.
* Contract position until April 2027 initially
* £200-250 per day
This role plays an important part in ensuring clinical studies are conducted in compliance with internal policies, regulatory standards, and approved research protocols.
The successful candidate will work closely with the clinical research team to support documentation, reporting, and coordination activities that contribute to the successful execution of clinical trials.
Key Responsibilities
* Provide operational and administrative support for ongoing clinical trials and research programs.
* Assist the clinical research team with preparing, reviewing, and maintaining safety reports and related documentation for investigators and relevant stakeholders.
* Ensure accurate documentation and reporting in line with clinical trial protocols, regulatory requirements, and internal policies.
* Record and escalate technical complaints, adverse events, and special case scenarios related to pharmaceutical products in accordance with established procedures.
* Apply company policies and standard operating procedures to resolve routine operational issues.
* Collaborate with supervisors and cross-functional teams to support clinical research activities and project delivery.
* Maintain well-organized records, databases, and documentation related to clinical trials.
* Support the distribution and tracking of marketing samples where applicable.
* Follow established processes and detailed instructions to ensure tasks are completed accurately and on time.
About You
* Strong organisational and documentation skills
* Ability to follow structured processes and regulatory requirements
* Excellent attention to detail and accuracy
* Strong communication and collaboration skills