{"id":1668104,"url":"https://alion.io/job/-goldbelt-senior-clinical-research-program-manager","title":"Senior Clinical Research Program Manager","company":{"id":1905594,"name":"Goldbelt","domain":"goldbelt.com","url":"https://alion.io/company/goldbelt","size_band":"501-1000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"iCIMS","truth_index":null},"role":"Management","role_family":"Management","seniority":"senior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Portsmouth, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":90000,"max_usd":168000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":4487},"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"HIPAA","optional":false},{"name":"Matter","optional":false}],"status":"live","first_seen_at":"2026-10-02T06:16:20Z","employer_posted_date":"2026-10-02","last_verified_at":"2026-10-20T09:11:58Z","board_verified":true,"closed_at":null,"days_open":18,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":18},"description":"Overview\nPlease note that this position is contingent upon the successful award of a contract currently under bid.\nGoldbelt Apex, a part of the Healthcare Technology Transformation Group, is a data-focused company dedicated to process and quality in every aspect. As experts in healthcare IT experts, Apex is committed to building systems for healthcare organizations to seamlessly communicate and exchange data across different systems and devices.\nSummary:\nPlease note that this position is contingent upon the successful award of a contract currently under bid.\nGoldbelt is seeking a Senior Clinical Research Program Manager to support the Naval Medical Center Portsmouth (NMCP) Clinical Investigation Department (CID) in Portsmouth, Virginia. This position serves as the Clinical Program Manager and Government-designated Key Personnel for the contract.\nThe Senior Clinical Research Program Manager provides scientific leadership, research regulatory expertise, personnel supervision, and overall program management for contractor-supported clinical research activities at NMCP.\nThis is a senior clinical/scientific research leadership position requiring demonstrated experience with IRB- and/or IACUC-regulated research. The Program Manager serves as a research Subject Matter Expert (SME), provides continuity and sustainability across clinical and combat casualty care research programs, supervises multidisciplinary contractor research personnel, and maintains day-to-day authority for contractor task order performance.\nThe position supports research and scholarly activities involving the Combat Trauma Research Group (CTRG), Otolaryngology, Pediatrics, Nursing Research, Orthopedics, Women's Health, Emergency Medicine, Graduate Medical Education (GME) programs, the CID Animal Facility (ANFAC), and other NMCP research stakeholders.\nThe research portfolio encompasses human-subject and animal research, Institutional Review Board (IRB) and Institutional Animal Care and Use Committee (IACUC) protocols, Quality Improvement (QI), Quality Assurance (QA), exempt and non-human-subject research, and related scholarly activities.\nThis is a full-time, primarily onsite position at Naval Medical Center Portsmouth. Telework may be authorized in accordance with contract requirements and Government approval.\nResponsibilities\nEssential Job Functions:\nProvides overall leadership, management, and supervision of contractor personnel supporting NMCP clinical and scientific research activities.\nServes as the contractor's primary day-to-day management representative and maintains authority to act for the contractor on operational contract matters.\nProvides continuity and sustainability for contractor-supported clinical and combat casualty care research programs.\nServes as a research Subject Matter Expert (SME) supporting investigators conducting IRB- and IACUC-regulated studies.\nProvides scientific and regulatory research guidance to NMCP departments and research personnel.\nSupports Government Principal Investigators (PIs) and Clinical Protocol Developers in the formulation of research concepts, conceptual frameworks, study objectives, research strategies, and related scientific activities, subject to final Government approval.\nSupports research activities across the lifecycle from research concept and protocol development through execution, regulatory compliance, data collection, reporting, presentation, publication, and dissemination.\nMaintains and monitors research regulatory documentation, approval requirements, and associated timelines.\nMonitors protocol deviations and associated corrective actions.\nSupports research portfolio prioritization and alignment with the NMCP mission.\nTracks research data deliverables, reporting requirements, contract deliverables, milestones, and schedules.\nSupervises multidisciplinary contractor personnel supporting clinical protocol development, clinical research coordination, human-subject research, animal research, bioengineering/biomechanics, simulation, and related research activities.\nEnsures qualified contractor personnel are assigned and maintained across the program and monitors staffing vacancies and continuity risks.\nCoordinates contractor employee onboarding, Common Access Card (CAC) and access requirements, mandatory training, and personnel readiness.\nMaintains appropriate contractor supervision and the non-personal services relationship required for contractor personnel.\nEnsures contractor personnel comply with applicable IRB/IACUC protocols, research procedures, privacy requirements, and DoD/DHA requirements.\nSupports investigator-initiated human and animal research, regulatory submissions and amendments, informed-consent documentation, scientific review, IRB/IACUC coordination, research databases, specimen activities, study reporting, and related research functions.\nConducts research seminars for contractor personnel and coordinates Government-approved research training when authorized.\nAttends research conferences and meetings and supports development of scientific presentations when required.\nCoordinates with the Contracting Officer's Representative (COR), Contracting Officer, NMCP CID leadership, Government PIs, and other authorized stakeholders.\nEnsures accurate and timely contract reporting and tracking of applicable PWS and contract deliverables.\nSupports implementation of the contractor Quality Control Plan and identification and correction of performance deficiencies.\nSupports transition-in and transition-out activities and continuity of research operations.\nPerforms other duties directly related to successful performance of the clinical research support program.\nQualifications\nNecessary Skills and Knowledge:\nAdvanced knowledge of clinical, biomedical, health science, translational, or related scientific research.\nStrong knowledge of IRB- and/or IACUC-regulated research and associated protocol requirements.\nKnowledge of research protocol development, regulatory review, study execution, compliance monitoring, reporting, and dissemination.\nKnowledge of human-subject protection, research ethics, and regulatory compliance principles.\nDemonstrated ability to provide scientific and technical guidance to investigators, clinicians, scientists, research coordinators, and multidisciplinary research teams.\nDemonstrated ability to manage clinical/scientific research activities across the research lifecycle.\nStrong personnel leadership and supervisory skills in a multidisciplinary scientific or clinical environment.\nAbility to manage multiple research priorities, protocols, milestones, schedules, and deliverables simultaneously.\nAbility to identify and address research, regulatory, staffing, schedule, and performance risks.\nAbility to communicate effectively with senior Government, clinical, scientific, contracting, and research stakeholders.\nExcellent scientific, technical, written, verbal, organizational, and interpersonal communication skills. \nMinimum Qualifications:\nCandidates must meet one of the following education and experience combinations:Post-doctoral or medical doctoral degree in a biological science, health science, physiology, veterinary medicine, or related field, with a minimum of 3 years of relevant research experience; or\nMaster's degree in a biological science, health science, physiology, veterinary medicine, or related field, with a minimum of 5 years of relevant research experience.\n\nFor candidates qualifying through the Master's degree pathway:Must possess at least 5 years of experience supporting IACUC- and/or IRB-approved research protocols from development through dissemination.\n\nAdditional minimum requirements:Demonstrated experience supporting IRB- and/or IACUC-regulated research.\nDemonstrated experience with research protocol development, execution, compliance, and/or reporting.\nDemonstrated ability to lead or supervise research personnel or multidisciplinary scientific teams.\nAbility to work primarily onsite at Naval Medical Center Portsmouth in Portsmouth, Virginia.\nMust be available during required Government coordination hours, including 0800-1630 Monday through Friday, except Federal holidays and Government administrative closures.\nMust be able to satisfy applicable DoD/DHA personnel security, background investigation, CAC, privacy, HIPAA, training, and installation access requirements.\nMust be able to provide a current resume/CV and signed Letter of Intent (LOI) for inclusion in the proposal as Key Personnel.\n\nPreferred Qualifications:\nDoctoral-level degree (PhD, MD, DVM, or equivalent) in a biological, biomedical, health science, physiology, veterinary medicine, or closely related field.\nExperience supporting clinical research within the Department of Defense (DoD), Defense Health Agency (DHA), Military Health System (MHS), Department of Veterans Affairs (VA), or another federal healthcare/research organization.\nPrevious experience within a Military Treatment Facility (MTF), academic medical center, clinical investigation program, or comparable complex research environment.\nExperience supporting investigator-initiated clinical research.\nExperience managing both human-subject and animal research portfolios.\nExperience with combat casualty care, trauma, emergency medicine, or military-relevant clinical research.\nExperience with clinical trials, clinical research operations, or clinical protocol development.\nExperience with research portfolio management and prioritization.\nExperience supporting scientific publications, presentations, or research dissemination.\nExperience with Graduate Medical Education (GME) research and scholarly activities.\nExperience supporting Quality Improvement (QI) and Quality Assurance (QA) research or scholarly projects.\nExperience with ClinicalTrials.gov, electronic IRB systems, or comparable research management platforms.\nPrevious experience managing multidisciplinary personnel under a federal Government services contract.\nPay and Benefits\nThe salary range for this position is $135,000.00 to $165,000.00 annually\nAt Goldbelt, we value and reward our team's dedication and hard work. We provide a competitive base salary commensurate with your qualifications and experience. As an employee, you'll enjoy a comprehensive benefits package, including medical, dental, and vision insurance, a 401(k) plan with company matching, tax-deferred savings options, supplementary benefits, paid time off, and professional development opportunities.","description_format":"text","description_chars":10489,"description_truncated":false,"requirements":{"experience_years_min":5,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"master","optional":true},"security_clearance":false,"languages":[]},"benefits":["Professional development","Vision insurance"],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Biomedical Engineering"],"lifecycle":[{"event":"open","at":"2026-10-02T06:16:20Z"}],"visa":[],"liveness":{"score":26,"band":"fade","label":"Fading","p_open":1,"p_active":0.752,"p_room":0.35,"age_days":17,"expected_fill_days":8,"reasons":["conf:1","velocity","win:tail"],"computed_at":"2026-10-20T05:45:00Z"},"pay":null,"html_url":"https://alion.io/job/-goldbelt-senior-clinical-research-program-manager","json_url":"https://alion.io/job/-goldbelt-senior-clinical-research-program-manager.json","meta":{"generated_at":"2026-10-20T11:23:01Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":12509,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-10-21T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":1905594},"rest":"https://alion.io/mcp/rest/get_company?id=1905594"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2F-goldbelt-senior-clinical-research-program-manager"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2F-goldbelt-senior-clinical-research-program-manager"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2F-goldbelt-senior-clinical-research-program-manager"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/-goldbelt-senior-clinical-research-program-manager\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2F-goldbelt-senior-clinical-research-program-manager"}]}