Clinical Research Specialist
1 week ago
Drive innovation in clinical research as a Clinical Research Associate, contributing to the design and analysis of trials, interpreting complex medical data.
A successful candidate will have in-depth knowledge of trial processes, regulations, and guidelines. They should be able to work independently and collaboratively, with excellent organizational and communication skills.
Key Responsibilities- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborate with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation.
- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 4 years of experience as a Clinical Research Associate.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
The ideal candidate will be detail-oriented, proactive, and results-driven, with the ability to work in a fast-paced environment.
They should possess strong organizational skills, with the ability to prioritize tasks and manage multiple projects simultaneously.
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