CLINICAL RESEARCH COORDINATOR III
General Responsibilities
To serve as a lead coordinator by providing oversight to less experienced staff to ensure quality and regulatory compliance with clinical research operations.
To coordinate and manage the research study lifecycle from start-up through close-out.
To coordinate and conduct all applicable clinical and administrative activities required by the protocol such as screening, scheduling, consenting, assessing, ordering, collecting, documenting and shipping under the auspices of Good Clinical Practice (GCP).
Requirements
Bachelor's degree in a related field and five (5) years of related experience required.
Work experience may NOT substitute for education requirement.
Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification preferred.
Preferences
- Experience working with or a strong demonstrated interest in sexual and gender health or related areas of health disparities.
- Experience working with community-based organizations, coalitions, or advocacy groups serving LGBTQ communities.
- Competence and experience in interpreting qualitative and quantitative research findings, and linking research or program data to written, oral, or visual products.
- Publishation record or contributions to research products (publications, reports, briefs, or other products) focused on sexual and gender health.
- Experience conducting statistical analyses with large or complex health datasets.
Qualifications
Excellent written and verbal communication skills, including the ability to summarize findings clearly and concisely for policy, community, and public audiences.
Strong organizational skills and ability to manage multiple rapid-turnaround projects and deadlines simultaneously.
Self-starter, ability to work independently.
Benefits
N/A
Pay
$60,835 - $75,000 Annual Salary Range
Schedule
Day/1st Shift
Hybrid Eligible