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Clinical Research Specialist I - Gender Surgery

Boston, MA, United States

Posted on
Jan 05, 2021

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57231BRTitle:Clinical Research Specialist I - Gender SurgeryDepartment:Plastic SurgeryAutoReqId:57231BRStatus:Full-TimeStandard Hours per Week:40 Job Category:ResearchJob Posting Description:

At Boston Children’s Hospital, success is measured in patients treated, parents comforted, and teams taught. It’s in discoveries made, processes perfected, and technology advanced. In major medical breakthroughs and small acts of kindness. And in colleagues who have your back and patients who have your heart. As a teaching hospital of Harvard Medical School, our reach is global and our impact is profound. Join us and discover how your talents can change lives. Yours included.

The Center for Gender Surgery offers gender-affirming care to adolescents and young adults. Our research is focused on access issues for gender affirming surgery as well as surgical outcomes. We primarily do quantitative research, but also collaborate on qualitative and mixed methods studies.

The Clinical Research Specialist I will be responsible for:

Assisting Principal Investigators (PIs) in planning and implementing clinical research studies as assigned. Coordinating preparation of protocol applications for submission to the IRB, sponsor, or regulatory authority. Corresponding with the IRB, study sponsors, clinical research organizations, study participants and referring physicians.
Recruiting study participants for enrollment in clinical trials and other research studies. Following individual study protocols. Completing informed consent procedures as assigned. Organizing strategies for recruiting study participants, screening study participants for eligibility on the telephone, in the clinic and other settings as required. Completing follow up with study participants in prescribed settings as required.
Organizing study procedures and scheduling study participants for study visits. Assisting the PI during patient visits. Performing study procedures designated for the Study Coordinator.
Completing record abstraction of source documents, conducting required study measurements, and completing study Case Report Forms in accordance with best practice methods. Conducting a QC check of completed CRFs prior to submission for data entry; coordinating resolution of all data queries. Completing data entry.
Complying with all institutional policies and government regulations pertaining to human subjects protections. Maintaining regulatory binders, case report forms, source documents, and other study documents. Monitoring the occurrence of clinical adverse events, reporting any to the PI, the study sponsor and Committee on Clinical Investigations. Updating protocol and amendment changes.
Assisting investigators in preparing articles for journal publication. Performing literature searches. Attending applicable courses and meetings offered by Clinical Research Program.

To qualify, you must have:

Bachelor's degree, and a minimum three years of relevant work experience, or Masters of Science or Masters of Public Health and one year of relevant work experience.
The analytical skills to collect information from diverse sources, apply professional principles in performing various analyses, and summarize the information and data to solve problems.
Communication skills to effectively deal with conflicting views or issues and mediate fair solutions, and well-developed writing skills
Interest in, and ideally experience with, working with gender diverse study participants and staff.
Willingness to engage with training around cultural competence for working with diverse study participants and staff.

Please note: During a public health emergency, individuals in this role may be expected to take on additional duties to respond to organizational needs.

Boston Children’s Hospital is an Equal Opportunity / Affirmative Action Employer. Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, sexual orientation, gender identity, protected veteran status or disability.

Office/Site Location:BostonRegular, Temporary, Per Diem:Regular

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