New

Senior Clinical Research Coordinator - OUD Genomics

Massachusetts General Hospital
United States, Massachusetts, Somerville
335 Revolution Drive (Show on map)
Apr 21, 2026
The Brain Bioethics Lab in the Department of Neurosurgery is seeking a full-time Senior Clinical Research Coordinator (CRC-Senior) to join our team. The CRC-Senior will oversee regulatory and operational needs for an NIH-funded study examining the ethical, clinical and legal challenges associated with the use of genetic tests for substance use disorders in clinical care. The CRC-Senior will help develop and implement the study's standard operating procedures, assist with onboarding and training of junior clinical research coordinators (CRCs), and ensure high-quality study execution and compliance. The CRC-Senior will also contribute to project execution, including employing qualitative and survey methods to collect and analyze data, and assist with manuscript preparation. This position is ideal for candidates with prior research experience who are ready to take on higher-level, independent, program development responsibilities. Summary Following established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, etc.; maintaining and updating data generated by the study. Additionally, it provides input into determining study subject suitability and input into recruitment strategy. Performs data analysis, interpretation, QA/QC, and assists in completing reports and presentations. Does this position require Patient Care? No Essential Functions -Assists with determining the suitability of study subjects and acts as a resource for patients and families. -Has input into recruitment strategies and may contribute to protocol recommendations. -Administers scores and evaluates study questionnaires. -Maintains research data, patient files, regulatory binders, and study databases. -Performs data analysis and QA/QC checks and organizes and interprets data. -Assists with preparation for annual review and assists PI in completing study reports and presentations. -May assist with training and orientation of new staff members. Education Bachelor's Degree Science required Can this role accept experience in lieu of a degree? Yes Licenses and Credentials Experience Related post-bachelor's degree research experience 1-2 years required Knowledge, Skills and Abilities - Ability to work more independently and as a team member. - Computer literacy, analytical skills, and ability to resolve technical problems. - Ability to interpret the acceptability of data results. - Working knowledge of data management programs. Key Responsibilities Leadership, Training, and Program Development Oversee study operations and assist with coordinating all study activities between the Brain Bioethics lab and external collaborators. Assist with development of standard operating procedures and quality assurance systems for study Contribute to creation of study templates, database management, and training materials for new study staff Train and mentor entry-level CRCs and study interns, ensuring adherence to the lab's standard operating procedures and best practices. Study Coordination and Execution Work with study PIs to manage day-to-day study activities, including study recruitment, coordination and scheduling of study interviews, and coordination of team meetings. Develop and maintain project timelines, recruitment benchmarks, and operational workflows. Assist with data collection (semi-structured interviews, surveys, chart reviews) and quality control checks, using REDCap, EPIC, and other programs. Assist with data analysis (qualitative interview data and quantitative survey data) using Dedoose, Excel, R, and other programs. Assist with preparation of manuscripts and presentations to disseminate study findings. Regulatory and Compliance Prepare and maintain Institutional Review Board (IRB) protocol submissions, amendments, and continuing reviews. Ensure compliance with study protocols, Human Subjects and Good Clinical Practice guidelines, and institutional policies. Prepare progress reports for key stakeholders and funders. Preferred Education & Experience Bachelor's degree required (genetics, health sciences, social sciences, psychology, public health, neuroscience, or related field preferred); Master's degree in one of the above areas is preferred. Minimum of 3-5 years of post-baccalaureate research experience in human subjects research including direct experience with IRB/regulatory documentation. Experience with building recruitment and data collection pipelines to execute both qualitative and quantitative data collection Experience analyzing and reporting findings from mixed-methods studies Skills & Competencies Ability to oversee and train others effectively. Strong organizational, time management, and problem-solving skills. Demonstrate a high degree of flexibility in accepting work assignments with the ability to effectively prioritize tasks, understand processes, and resolve issues Excellent interpersonal and written/verbal communication skills. Ability to work independently and collaboratively across multiple investigators and teams. The General Hospital Corporation is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.