Clinical Research Associate
4 days ago
We are seeking a highly skilled Clinical Research Coordinator to support our team in managing and coordinating clinical trials and research studies. The ideal candidate will have a strong understanding of regulatory guidelines and protocols, as well as excellent communication and organizational skills.
Key Responsibilities:- Coordinate and oversee all aspects of clinical trials, including participant recruitment, enrollment, and follow-up.
- Assist in the development of study protocols, consent forms, and data collection tools.
- Ensure all research activities comply with ethical standards, institutional policies, and regulatory requirements.
- Collect, manage, and analyze clinical data; maintain accurate and organized records.
- Communicate with study sponsors, monitor study progress, and resolve any issues that arise.
- Schedule and conduct participant visits, ensuring compliance with study protocols.
- Assist with the preparation of regulatory documents and reports.
- Maintain confidentiality and protect the integrity of participant data.
Requirements:
- Strong understanding of clinical research principles and regulatory guidelines.
- Excellent communication and organizational skills.
- Ability to work independently and as part of a team.
- Strong attention to detail and ability to maintain accurate records.
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