Clinical Research Coordinator na Boston Children's Hospital

Full-Time

40

Research

Department Summary:
This position will be housed in the Division of Gynecology. The Division sees a wide variety of pediatric and adolescent gynecology patients and research interest include health disparities, endometriosis diagnosis and treatment, intersex conditions, and gender affirming care. This role is the senior research coordinator role for the department, where you will be working with 5 gynecology attendings and one scientist on a variety of projects across the topics above.  This is a hybrid role involving some in person consenting (as needed).

Key Responsibilities:

• Assists Principal Investigators PIs in planning and implementing clinical research studies as assigned. Under the direction of the PI, coordinates preparation of protocol applications for submission to the IRB, sponsor, or regulatory authority. As directed by the PI corresponds with the IRB, study sponsors, clinical research organizations, study participants, and referring physicians.
• Recruits study participants for enrollment in clinical trials. Follows individual study protocols. Completes informed consent procedures as assigned. Organizes strategies for recruiting study participants and screens study participants for eligibility on the telephone, in the clinic, and other settings as required. Completes follow-up with study participants in prescribed settings as required.
• Organizes study procedures and schedules study participants for study visits. Assists the PI during patient visits. Performs study procedures designated for the Study Coordinator.
• Completes record abstraction of source documents, conducts required study measurements, and completes study Case Report Forms in accordance with best practice methods. Conducts a QC check of completed CRFs prior to submission for data entry; coordinates resolution of all data queries. Completes data entry as warranted.
• Complies with all institutional policies and government regulations pertaining to human subjects' protections. Maintains regulatory binders, case report forms, source documents, and other study documents. Monitors the occurrence of clinical adverse events, reporting any to the PI, the study sponsor, and Committee on Clinical Investigations IRB. Updates protocol and amendment changes.
• Assists investigators in data and/or document preparation for journal publication. Performs literature searches and pulls articles.

 
Minimum Qualifications
Education:

• Bachelor’s degree is required. Master’s degree preferred.

Experience:

• Bachelor’s with three years of relevant work experience OR Master’s degree and 1 year of relevant work experience.
• Comfort with reproductive and sexual health topics.
• Comfort with transgender health topics.
• Willingness to ask questions and openness to learning.

 
Boston Children’s Hospital offers competitive compensation and unmatched benefits including flexible schedules, affordable health, vision and dental insurance, child care and student loan subsidies, generous levels of time off, 403(b) Retirement Savings plan, Pension, Tuition and certain License and Certification Reimbursement, cell phone plan discounts and discounted rates on T-passes. Experience the benefits of passion and teamwork.

Boston

Regular

Part Remote/Hybrid