Clinical Scientist
CK Group have a fantastic opportunity for a Clinical Scientist to join an excellent pharmaceutical company on a full-time, contract basis (18 months).
Where:
Beerse, Belgium. Hybrid role.
The Role:
The Clinical Scientist will:
- Participate in adjudication committees to monitor patient adverse events.
- Be responsible for oversight and high-quality implementation and closure of the study, ensuring data integrity.
- Participate in vendor oversight focusing on the integration of data and technology in clinical trials.
- In concert with operational staff, acts as a liaison between the company and clinical investigators for overarching scientific guidance and other potential non-medical aspects.
- Be responsible for the TA review and sign off on various operational plans.
- Be Responsible for scientific input into HA and EC responses.
- Lead data visualization (DV) meetings and ensures decisions are documented and communicated internally and externally.
- Qualified CS may perform aspects of medical review under supervision of CL or SRP.
Requirements:
- Right to work in the EU is essential.
- PhD in relevant field (neuro, biology, chem, pharmacy,) PharmD or MD degree.
- Experience supporting clinical studies (later stage preferred Phase II - III).
- Experience in clinical research/drug development that has exposed the individual to the rigors of human trial conduct with pharmaceuticals, devices, basic clinical practice with the precepts of Good Clinical Practice.
Apply:
Right to work in the EU is essential. Please quote job reference T56732 in all correspondence.