Senior Clinical Research Associate
72% Flex
Offer summary
Qualifications: At least three years clinical monitoring experience and/or relevant clinical trial experience, Relevant life science degree or related field, Sound medical terminology knowledge, Strong communication and interpersonal skills.
Key responsabilities:
- Govern quality standards for trial monitoring activities
- Conduct site visits, ensure project guidelines and monitoring compliance
- Prepare regulatory documents, maintain Trial Master/File
- Provide in-house review of CRFs, assist with study audits and inspections
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
- Attention to detail, ability to prioritize tasks effectively
- Strong organizational and leadership qualities
- Excellent communication in English and local language
- Ability to work independently and collaborate within a team
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