Sr. Clinical Research Associate Contractor (Iceland)
72% Flex
Offer summary
Qualifications: At least 4 years of clinical monitoring experience or relevant clinical trial experience, Relevant life science, medical, nursing degree or equivalent education and experience, Strong oncology therapeutic background and CRO industry knowledge.
Key responsabilities:
- Independently control and monitor investigational sites ensuring compliance with protocols and regulations
- Assist in developing trial processes and documents, conduct feasibility assessments
- Track study data, ensure punctual reporting, supervise quality standards for trial monitoring activities
Job description
Required profile
Experience
Level of experience :
Mid-level (2-5 years)Industry :
Spoken language(s)
Check out the description to know which languages are mandatory.
Soft Skills
- Excellent team player with strong building abilities
- Proactive problem solver with analytical mindset
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