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Clinical Research Coordinator
A Clinical Research Coordinator manages and coordinates clinical trials, ensuring compliance with protocols and regulatory requirements
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Job Description
As a Clinical Research Coordinator, you will be responsible for coordinating and overseeing clinical trials, ensuring compliance with protocols, and facilitating communication between research teams and participants.
Purpose
To support and facilitate the execution of clinical research studies, contributing to medical advancements and patient care.
Duties and Responsibilities
- Coordinate and oversee clinical trials.
- Ensure compliance with study protocols and regulations.
- Recruit and screen research participants.
- Collect and manage study data.
- Communicate with study sponsors, investigators, and participants.
Qualifications
- Bachelor's degree in a healthcare or science-related field.
- Certification as a Clinical Research Professional (CCRP) or equivalent.
- Knowledge of clinical research regulations and protocols.
- Strong organizational and communication skills.
Experience
- Entry-level positions may require clinical research experience or internships.
- Mid-level roles typically require 2-4 years of clinical research coordination.
Preferred Qualifications
- Advanced certification in clinical research coordination.
- Continued education in clinical research.
Working Conditions
- Office-based work with occasional site visits.
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