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Responsibilities:
- Coordinate clinical research studies from start to finish
- Recruit and screen potential participants for eligibility
- Obtain informed consent from participants and ensure compliance with ethical standards
- Collect and analyze data, including blood samples, using appropriate clinical laboratory techniques
- Monitor participants' progress throughout the study and address any concerns or adverse events
- Collaborate with healthcare professionals, including nurses and physicians, to ensure proper care and treatment of participants
- Maintain accurate and up-to-date documentation of study activities and participant records
- Adhere to regulatory standards and guidelines for clinical research, including Good Clinical Practice (GCP) standards
Skills:
- Strong knowledge of clinical research principles, practices, and regulations
- Proficiency in statistical software for data analysis
- Experience in clinical development and conducting clinical trials
- Ability to perform blood sampling and other clinical procedures as required
- Excellent organizational skills with attention to detail
- Strong analytical skills to research, analyze, and interpret complex data sets
- Effective communication skills to collaborate with multidisciplinary teams and communicate study findings
Please note that this job description is not exhaustive and additional responsibilities may be assigned as needed.
Job Type: Full-time
Pay: $23.00 - $25.00 per hour
Benefits:
Location:
Ability to Relocate:
Work Location: In person
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