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Senior Clinical Research Coordinator
Medix™ • Pearland, TX 77588 • Posted 1 day ago via LinkedIn
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In-person • Full-time • Senior Level
Job Highlights
Using AI ⚡ to summarize the original job post
We are seeking a Senior Clinical Research Coordinator with phlebotomy experience to oversee and coordinate clinical trials. The role involves managing study activities, ensuring protocol compliance, performing blood draws and specimen collection, and maintaining accurate study documentation. The ideal candidate will have excellent organizational skills, strong attention to detail, and experience in clinical research and phlebotomy.
Responsibilities
- Coordinate and manage the day-to-day operations of clinical trials
- Perform venipunctures and other specimen collection procedures
- Ensure proper labeling, processing, and storage of biological samples
- Maintain accurate and up-to-date study documentation
- Monitor participant safety and report any adverse events
- Ensure compliance with study protocols, regulatory guidelines, and ethical standards
- Liaise between investigators, sponsors, and study participants
- Assist with participant recruitment, screening, and consent process
- Manage and enter data into electronic data capture (EDC) systems
Qualifications
Required
- Experience in clinical research
- Experience in phlebotomy
- Excellent organizational skills
- Strong attention to detail
- Ability to ensure compliance with study protocols, regulatory guidelines, and ethical standards
Full Job Description
We are looking for a dedicated Clinical Research Coordinator with phlebotomy experience to manage and oversee clinical trials. The candidate will be responsible for coordinating study activities, ensuring protocol compliance, and performing blood draws and specimen collection. This position requires excellent organizational skills, strong attention to detail, and experience in clinical research and phlebotomy.
Key Responsibilities:
- Coordinate and manage the day-to-day operations of clinical trials
- Perform venipunctures and other specimen collection procedures
- Ensure proper labeling, processing, and storage of biological samples
- Maintain accurate and up-to-date study documentation
- Monitor participant safety and report any adverse events
- Ensure compliance with study protocols, regulatory guidelines, and ethical standards
- Liaise between investigators, sponsors, and study participants
- Assist with participant recruitment, screening, and consent process
- Manage and enter data into electronic data capture (EDC) systems
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