Centessa Pharmaceuticals plc is seeking a Sr. Clinical Trial Associate (Contract) to support the planning and execution of clinical studies across one or more clinical trials. The role will work closely with the Clinical Trial Manager to ensure site start-up through close-out activities are conducted in accordance with SOPs, GCP and regulatory guidelines.
Requirements
- B.A. or B.S. degree required
- 4+ years' experience within a biotech or pharmaceutical organization
- Experience working with clinical sites, principal investigators, clinical operations staff and CROs a plus
- Knowledge and training on Good Clinical Practice (GCP) for clinical research studies
- Computer skills including proficiency with Microsoft Office software
- Independently motivated, detail oriented and good problem-solving ability
- Excellent written and verbal communication skills
- Flexible and able to adapt to new situations as the business demands
- Ability to work effectively from a virtual home office setting