Clinical Research Coordinator

in Healthcare + Life Sciences Contract

Job Detail

  • Experience Level Mid Level
  • Degree Type Bachelor of Science (BS)
  • Employment Part Time
  • Working Type On Site
  • Job Reference 0000014223
  • Salary Type Hourly
  • Industry Medical Devices
  • Selling Points

    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.

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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