Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham.
Job Summary
The Mapping & Engineering Neural Dynamics (MEND) Lab (https://www.rolstonlab.com/) within the Department of Neurosurgery at Brigham & Women’s Hospital is a human neural engineering laboratory that uses electrophysiological recordings and advanced imaging to understand the brain. We are particularly focused on diseases where brain activity is changed, like epilepsy, tremor, pain, and psychiatric disorders. Our research in understanding brain activity is combined with methods of changing brain dynamics, like electrical stimulation, to better treat these disorders with or without neurosurgical interventions. The laboratory, led by Dr. John Rolston MD, PhD is seeking a motivated and talented individual to serve as the Clinical Research Program Manager for our dynamic team.The Clinical Research Program Manager is responsible for the administrative management and support of all research projects conducted within the clinical and research practice of the PI, Dr. John Rolston.
The MEND Lab is involved with multiple NIH, foundation and industry-sponsored studies. The Clinical Research Program Manager will support multiple active human protocols at any given time, will maintain standard operating procedures, and train new staff members to ensure compliance. The incumbent will have the lead administrative role in preparing/submitting new grant proposals (in conjunction with the department’s Grant Administrator) coordinating Data Use and Confidentiality Agreements as well as coordinating the development of IRB protocols and amendments.
With oversight by the department Research Administrator, the Clinical Research Program Manager will manage project budgets throughout the project lifecycle. The Clinical Research Manager also oversees the development and refinement of the lab’s Standard Operating Procedures, ensuring adherence to regulatory requirements, including Good Clinical Practices (GCP), 21 CFR Part 11, HIPAA, etc.
Qualifications
PRINCIPAL DUTIES AND RESPONSIBILITIES
Interface with multiple research groups from various clinical departments within BWH and Mass General Brigham and external academic collaborators, as well as sponsors, clinical sites, central laboratories and third-party vendors, and other groups involved in clinical trials.Organize project team meetings and prepares the agenda under direction of the PI.Serve as primary liaison with the IRB, ancillary research committees, and Human Research Compliance Office.Serve as primary liaison with regulatory offices, oversee audits, and work with study staff to address findings.Assist with grant proposals, just-in-time submissions, and clinical trial agreements.Prepare and monitor project budgets and sponsor invoices.Serve as primary liaison with departmental staff for onboarding interns, student trainees, research staff, associates, and collaborators.Manage and oversee the trial lifecycle and clinical trial operations, including site feasibility questionnaires, evaluation and initiation, subject visits, and study closeout. Serve as primary point of contact for IRB, ancillary review committees, and sponsor and affiliated contract research organizations.Receive, negotiate, and execute nondisclosure/confidentiality agreements, in collaboration with institutional financial analysts, research directors, legal counsel, and principal investigator.Maintain Standard Operating Procedures (SOPs) for the research program, including the modification of existing SOPs and development of new SOPs.Enter non-clinical trial data in functional neurosurgery research databases created and maintained by the lab.Overseeing procurement of lab equipment and supplies.Train new staff as necessary on study protocols and standard operating procedures.Edit and submit manuscripts in collaboration with the Principal Investigator.Work with investigators and research staff to ensure clinical trials are conducted in accordance with all SOPs, GCP, GLP and FDA regulations.Assist in the preparation and hosting of monitoring visits, Sponsor audits and FDA inspections.Perform electronic data capture (EDC) entry, resolve EDC queries, and manage clinical trials documentation such as subject records and correspondence, essential documents, trial operations manuals, and Instructions for Use.Work with PI and physician assistant to identify and screen appropriate candidates for trial participation and evaluate inclusion/exclusion criteria, per study protocol. Obtain necessary approvals, patient informed consent, and demographic and screening information required for patient enrollment. Contact patients and/or families via written and telephone communications for the purpose of explaining the nature of studies and setting up visits and interviews.Arrange and coordinate scheduling of initial assessment and subsequent assessments as outlined in study protocols.Monitor study by gathering information and reviewing materials, visiting patients in the study, discussing problems, and exchanging information with clinical team.Function as liaison between research participants and other members of the team during the study; assess learning needs and educate patients and family as appropriate. Document study visits, submit expense reports for subject payments/stipends and reimbursement, and prepare and submit Sponsor invoices.Represent the PI and lab at meetings when needed.SKILLS/ABILITIES/COMPETENCIES REQUIRED
Experience with, or desire to obtain working knowledge of diseases treated by functional neurosurgery (including epilepsy, Parkinson’s disease, dystonia, essential tremor, psychiatric diseases) and strong desire to contribute to translational neuroscience.Demonstrated understanding and knowledge of the methods, materials, and equipment used in research laboratory activities.Exceptional organizational and time management skillsAbility to track project milestones/progress digitally, on a daily, weekly, monthly basisAbility to apply the same level of effort to remote work as to onsite workSuperb interpersonal skillsStrong ability to interact effectively with many different people and levels throughout the institution and within as well as outside the hospital setting, including patients, doctors, nurses, grant administrators, researchers, etc. Excellent written grammarWillingness to pick up the phone and call someoneto interact with colleagues, patients and families, other clinical and academic sites, NIH, sponsors, CROs, vendors, etc.Ability to work independently and as a member of a team.Excellent Analytical skills and ability to problem-solve.Flexibility to meet the demands of the work and the lab.Flexibility to accommodate shifting priorities and changes in the PI’s scheduleto effectively manage team tasks and urgent timelinesUnderstanding of REDCap system – Research Electronic Data CaptureUnderstanding of laws, regulations, and standards governing clinical trial conduct, Standard Operating Procedures, regulatory audits, and clinical trials documentation requirementsEfficient use of software programs such as MS Office Suite, Google docs, Dropbox, etc.Ability to prepare/monitor budgetsAbility to work independently, introduce innovations, identify problems, and develop solutionsEDUCATION
MA/MS degree is required, PhD in neuroscience, biomedical engineering, or a closely related field preferred.WORKING CONDITIONS
The Research Program Manager will collaborate with a team of postdoctoral fellows, graduate students, physician-scientists, administrators, clinical research coordinators. Work will be performed in both the laboratory setting and clinical facilities within the hospital. The ability to work a remote/on-site hybrid schedule is offered with supervisor approval. There must be a willingness to work at night and occasionally work on weekends as required.EEO Statement
BWH is an Affirmative Action 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.
Additional Job Details (if applicable)
Remote Type
Hybrid
Work Location
60 Fenwood Road
Scheduled Weekly Hours
40
Employee Type
Regular
Work Shift
Day (United States of America)
Pay Range
$62,004.80 - $90,750.40/Annual
Grade
7
EEO Statement:
The Brigham and Women's Hospital, Inc. is an Equal Opportunity Employer. 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. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran’s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources at (857)-282-7642.
At Mass General Brigham, our competency framework defines what effective leadership “looks like” by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.