Senior CRA
Reference:
Job Type: Permanent
Location: United Kingdom, United Kingdom_Home based,
Salary: Competitive
Start Date: ASAP
Duration: Permanent
Summary
Planning, implementation, monitoring and evaluating international multi-centre regulatory and PMS studies.
All studies performed to the highest ethical, clinical and scientific standards
Key Tasks:
- Management of junior clinical staff - CRA and CTA
- Preparation of Clinical Investigatior Brochures
- Writing of Protocols (CIP)
- Designing CRF
- Preparation of submission to CA and Ethics committees
- Site Initiation visits
- Monitoring studies to ISO 14155
- Management of Study Data
- Following company SOP
Specific Requirements
- Degree qualified in Life Sciences
- 2-3 years experience of monitoring clinical studies
- Will consider Pharma experience
- This role is office based
- European travel required
Apply for this job
Applications are handled online where you will be able to upload your CV.
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