Clinical Trial Associate
Job Summary
Supporting the design and management of clinical trials, the full-time remote Clinical Trial Associate will assist in planning, execution, and monitoring of trials while ensuring adherence to protocols and regulatory guidelines.
Key responsibilities
- Assist in planning, execution, and monitoring of clinical trials to ensure compliance with protocols and regulations
- Coordinate study activities including site initiation, patient recruitment, and data collection
- Maintain comprehensive study documentation and support study close-out activities, including data cleaning and report preparation
Required qualifications
- Bachelor's or advanced degree in Life Sciences, Health Sciences, or a related field
- Previous experience in clinical research or healthcare, preferably in the pharmaceutical, biotechnology, or CRO industry
- Strong organizational and time management skills with the ability to prioritize tasks
- Excellent attention to detail and problem-solving abilities
- Effective communication and interpersonal skills for cross-functional collaboration
Complete Job Description
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