Medical Research Professional
Há 6 dias
The primary focus of this role is to guarantee the integrity and quality of clinical trials from initiation to completion.
Key Responsibilities:- Conduct thorough site assessments, ensure protocol adherence, and verify data accuracy throughout the trial process.
- Maintain a strong working relationship with investigators and site staff to facilitate efficient study conduct.
- Perform in-depth data review, identify discrepancies, and resolve queries to maintain high-quality clinical data.
- Collaborate with cross-functional teams to develop and review study-related documentation.
- Relevant degree in a scientific or healthcare field.
- Minimum 2 years of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial procedures, regulations, and ICH-GCP guidelines.
- Excellent organizational, communication, and problem-solving skills.
- Ability to work independently and collaboratively in a fast-paced environment.
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Medical Research Professional
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