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Clinical Research Coordinator


PayCompetitive
LocationRichmond/Virginia
Employment typeFull-Time

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  • Job Description

      Req#: req7107_78wOjNxvg6Au
      Employer Industry: Healthcare Research

      Why consider this job opportunity:
      - Up to 5 remote days per month upon successful completion of training and leadership approval
      - Continuing education support for undergraduate and graduate tuition for a maximum of 6 credits per semester
      - Professional development opportunities encouraged, including certifications, seminars, and conferences
      - Generous leave policy: 28 vacation days, 12+ state holidays, and 4 days for volunteering
      - Comprehensive medical, dental, and vision benefits for employees and their eligible family members
      - Participation in the Virginia Retirement System (VRS) and other retirement saving options

      What to Expect (Job Responsibilities):
      - Support Principal Investigators in daily activities for clinical research studies, including feasibility assessments and participant eligibility
      - Recruit and educate participants about clinical trials and related patient care
      - Manage the collection, documentation, and analysis of clinical research data
      - Ensure compliance with federal and state regulations, as well as institutional policies
      - Maintain current certifications and training related to clinical research and human subjects protections

      What is Required (Qualifications):
      - Must have an understanding of clinical research management duties from initiation to closeout
      - Experience with data collection, processing, and management in clinical research
      - Current CITI credentials for Human Subjects Protections and Good Clinical Practice (GCP)
      - Familiarity with federal and state laws and regulations related to clinical research
      - Ability to work both collaboratively and independently in a research setting

      How to Stand Out (Preferred Qualifications):
      - Experience with electronic clinical research charts and data management systems
      - Previous involvement in patient recruitment and retention for clinical trials
      - Knowledge of IRB requirements and human subjects protection regulations
      - Additional certifications in clinical research management or related fields
      - Familiarity with community engagement strategies for research studies

      #HealthcareResearch #ClinicalResearch #CareerDevelopment #RemoteWork #HealthEquity

      "We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately. We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer."
  • About the company

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