Research Coordinator, Obstetrics and Gynecology (OBGYN)
$66,300–$69,300 year
On-siteNew York, United States
Job Summary
Maintain awareness of study regulatory status, assist with informed consent processes, and follow up with patients to ensure adherence to study requirements. Collect patient information through chart abstraction and data collection tools, then compile and analyze data for presentations to regulatory agencies and sponsors. Screen potential subjects for eligibility, schedule visits, and manage biospecimen inventory, tracking, and storage logistics. Prepare grant applications, draft study budgets, and generate preliminary measurement reports for Principal Investigators. Update Institutional Review Board documents and coordinate with the Office of Clinical Trials to maintain research approvals. Manage competing priorities across multiple studies while balancing operational demands and participant needs.
Required Qualifications
- Bachelor's degree in life sciences, allied health or equivalent in a related discipline
- 0-1 years experience or an equivalent combination of education and experience
- Effective oral, written, communication, interpersonal skills
- Ability to work under the direction of supervision
- Ability to operate research related equipment
- Proficiency in using various Microsoft Office applications such as Word, Excel, Access, Power Point and Outlook
- Familiarity with Internet applications
- Ability to identify, analyze and solve problems
- Time management skills and ability to work well under pressure
- Ability to effectively communicate with all levels of the organization
Desired Qualifications
- Prior experience working with research protocols, human subjects research, clinical research operations, or academic medical center research
- Experience with OBGYN, women's health, reproductive health, fertility, reproductive endocrinology, maternal-fetal medicine, or biospecimen-related research
- Familiarity with EPIC, REDCap, Qualtrics, institutional IRB systems, research tracking tools, EMR abstraction, consent documentation, and specimen tracking
- Ability to work collaboratively with faculty, clinical teams, research staff, patients, and external collaborators
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