Lead impactful clinical research projects with a focus on innovation and compliance. Collaborate with professionals in a dynamic, regulated environment. Opportunity for growth and potential permanent conversion.
Clinical Research Coordinator
in Healthcare + Life Sciences ContractJob Detail
Job Description
Overview
- Coordinate and oversee clinical research studies ensuring compliance with protocols and regulations.
- Develop and author clinical protocols and patient record forms for research studies.
- Manage operational aspects of clinical trials, including site and vendor selection.
- Interpret results of clinical investigations for drug, device, or consumer applications.
- Ensure adherence to Good Clinical Practice (GCP) and Standard Operating Procedures (SOP).
- Collaborate with project teams to achieve study objectives and milestones.
- Provide mentorship to junior professionals and contribute to cross-functional assignments.
- Deliver projects from design to implementation while adhering to policies and regulations.
Key Responsibilities & Duties
- Design, plan, and oversee clinical evaluation research studies ensuring compliance with regulatory standards.
- Prepare and author clinical protocols and patient record forms for study documentation.
- Conduct registered and nonregistered clinical studies for product evaluation.
- Interpret clinical investigation results for new applications and commercial potential.
- Resolve operational aspects of clinical trials in collaboration with project teams.
- Ensure compliance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOP).
- Manage clinical supply operations, site, and vendor selection processes.
- Provide guidance to entry-level professionals and support career stream employees.
Job Requirements
- Bachelor’s degree in engineering, life sciences, or related medical/scientific field required.
- Minimum of 2 years of experience in clinical research or related field.
- Knowledge and experience with CTMS, EDC, and TMF systems preferred.
- Proficiency in Good Clinical Practice (GCP) and regulatory compliance.
- Strong site management experience, either at site or sponsor level.
- Ability to work full-time on-site for a 40-hour workweek.
- Effective communication and collaboration skills within cross-functional teams.
- Potential for contract conversion to permanent position.
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