{"id":1647307,"url":"https://alion.io/job/beaufort-clinical-project-manager","title":"Clinical Project Manager","company":{"id":3854241,"name":"Beaufort","domain":"beaufort.com","url":"https://alion.io/company/beaufort-3","size_band":null,"is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":null,"truth_index":null},"role":"Management","role_family":"Management","seniority":"senior","employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"inferred_payroll_markers","remote_working_hours":null,"hiring_geo_confidence":"inferred","locations":[],"countries":[],"hiring_countries":["US"],"hiring_countries_total":1,"salary":null,"salary_estimate":{"min_usd":89000,"max_usd":174000,"period":"year","method":"global_role_seniority_cell","sample_n":5925},"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Matter","optional":false},{"name":"Smartsheet","optional":false}],"status":"live","first_seen_at":"2026-10-01T22:45:31Z","employer_posted_date":null,"last_verified_at":"2026-10-01T22:45:31Z","board_verified":false,"closed_at":null,"days_open":16,"trust":{"level":"not_scored","repost_count":null,"flags":[],"days_open":16},"description":"Beaufort seeks a skilled Clinical Project Manager (CPM) to work alongside a top-notch team of clinical researchers. We participate in an exciting and growing industry and that growth fuels the need to continue to build our team and support our mission.\n\nThis is a unique opportunity to join a growing CRO where your leadership will directly impact trial success and client satisfaction.\n\nPosition Summary\nThe Clinical Project Manager (CPM) leads the end-to-end delivery of clinical trials across diverse therapeutic areas, ensuring strategic alignment, operational excellence, and regulatory compliance. This role serves as a cross-functional leader and primary liaison between sponsors, vendors, and internal teams to drive successful trial outcomes.\n\nKey Responsibilities\nClinical Trial Oversight & Leadership\n\nProvide strategic and operational oversight for assigned clinical studies from start-up through close-out.\n\nLead the cross-functional project team (e.g., clinical operations, data management, statistics, safety, and medical writing) to meet or exceed project goals.\n\nAct as primary contact for Sponsors and serve as a Subject Matter Expert (SME) for designated clinical programs.\n\nEnsure compliance with ICH-GCP, SOPs, protocols, and regulatory requirements.\n\nProject Management\n\nCreate, manage, and maintain detailed project plans including timelines, deliverables, KPIs, and milestones.\n\nTrack project performance using appropriate systems, tools, and techniques (e.g., project dashboards, risk logs, scope change trackers).\n\nIdentify project risks and develop proactive mitigation strategies in collaboration with sponsors and internal stakeholders.\n\nImplement structured change control processes to manage protocol amendments or scope changes.\n\nLead regular internal and sponsor-facing status meetings, ensuring clear communication of project progress, challenges, and action items.\n\nProject Financial Management\n\nMonitor and reconcile project budgets.\n\nCollaborate with finance teams to provide accurate forecasts and manage scope creep.\n\nSupport financial performance analysis.\n\nSite and Vendor Management\n\nOversee site selection activities and review feasibility data to make final recommendations.\n\nProvide oversight and guidance to CRAs regarding monitoring activities, site management, and issue resolution.\n\nParticipate in or lead site qualification visits, initiation visits, interim monitoring visits, and close-out visits as needed.\n\nManage vendor performance and coordinate outsourced service providers to ensure quality and timelines.\n\nDocumentation and Reporting\n\nReview and/or contribute to key study documents such as protocols, CRFs, monitoring plans, site manuals, and data management plans.\n\nEnsure timely development and delivery of study reports, metrics, and sponsor communications.\n\nSupport regulatory submissions and audit readiness activities.\n\nTeam Support and Organizational Collaboration\n\nMentor junior team members, support team knowledge sharing and contribute to performance feedback.\n\nAssist with onboarding, and training of new clinical operations staff.\n\nProvide support for business development activities, participate in bid defenses and potential client meetings as needed.\n\nQualifications\nEducation & Certifications\n\nBachelor’s degree in biological sciences, pharmacy, nursing, or a related health discipline required; advanced degree preferred.\n\nCertification(s) such as PMP, CCRP, CCRA, or equivalent highly preferred.\n\nExperience\n\nMinimum of 5 years’ experience in clinical research with at least 3 years in a project management role.\n\nProven history of leading complex global or domestic clinical trials within a CRO or sponsor environment.\n\nExperience managing clinical studies in in vitro diagnostics (IVD) and Medical Device\n\nApplied deep knowledge of ICH-GCP and global regulatory requirements to ensure compliance across all phases of clinical trial execution.\n\nSkills & Competencies\n\nProven leadership and stakeholder management skills; able to influence across teams and drive project success.\n\nSkilled in managing multiple priorities and timelines in fast-paced, deadline-driven environments.\n\nExperienced in global trial execution with cultural awareness and adaptability.\n\nComfortable navigating ambiguity, making independent decisions, and knowing when to escalate.\n\nProficient in CTMS, eTMF (e.g., VeevaVault), and project management tools (e.g., MS Project, Smartsheet)\n\nCommitted to ethical conduct, client satisfaction, and continuous improvement.\n\nWork Environment & Expectations\n\nMust be able to work independently and collaboratively in a remote or office-based setting.\n\nAbility to travel occasionally to attend meetings, site visits, or client engagements.\n\nWhy Join Beaufort?\nBeaufort offers a different CRO experience. It’s not just about what we do, it’s how we do it. Together our team brings a level of passion knowledge and commitment to our projects and clients. We foster a culture of excellence clinical project management and regulatory support.\n\nAt Beaufort you will be part of industry leading expertise with a shared sense of purpose and unwavering accountability to help clients achieve successful market authorization.\n\nBeaufort is an equal opportunity employer and values diversity. We offer a highly competitive compensation and benefits package.\n\nOriginally posted on Himalayas","description_format":"text","description_chars":5373,"description_truncated":false,"requirements":{"experience_years_min":5,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":null,"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[{"name":"United States","iso":"US","kind":"country"}],"hiring_excludes":[],"relocation_offered":false,"industries":["Real Estate"],"lifecycle":[{"event":"open","at":"2026-10-02T00:01:17Z"}],"visa":[],"liveness":{"score":56,"band":"ok","label":"Likely open","p_open":0.85,"p_active":0.734,"p_room":0.9,"age_days":15,"expected_fill_days":29,"reasons":["seen:15","win:mid"],"computed_at":"2026-10-17T05:46:00Z"},"pay":null,"html_url":"https://alion.io/job/beaufort-clinical-project-manager","json_url":"https://alion.io/job/beaufort-clinical-project-manager.json","meta":{"generated_at":"2026-10-18T11:19:13Z","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":16791,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-10-19T00:00:00Z"}},"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":3854241},"rest":"https://alion.io/mcp/rest/get_company?id=3854241"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Fbeaufort-clinical-project-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%2Fbeaufort-clinical-project-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%2Fbeaufort-clinical-project-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/beaufort-clinical-project-manager\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Fbeaufort-clinical-project-manager"}]}