Last updated: 2025-05-22

36 Clinical Operations Management jobs in Boston.

Hiring now: Primary Research Coordina @ Clearview , Clinical Trial Associate @ Orchard Th, Medical Dir @ Atalanta T, Clinical Research Scienti @ Whoop, Clinical Trial Mgr @ Seaport Th, Data Team Lead @ Iqvia, Site Connect Strategist @ Veeva Syst, Dir Country Ops Managemen @ Astrazenec, Associate Dir Of Program @ Manifold B, Proj Coordinator @ Costello M.Explore more at at kaamvaam.com

šŸ”„ Skills

clinical trials (13) project management (9) clinical operations (9) clinical development (5) timelines (5) regulatory compliance (5) clinical trial management (5) regulatory submissions (4) cross-functional teams (4) budgets (4)

šŸ“ Locations

Boston (12) Cambridge (12) Waltham (8) Watertown (3) Somerville (1)

Clearview Healthcare Partners

Skills & Focus: market research, healthcare, biological sciences, expert network, project management, scheduling, communication, consulting, expertise, compliance
About the Company: ClearView Healthcare Partners is a premier life sciences strategy consulting firm headquartered in Boston, with offices in San Francisco, New York City, London…
Experience: Minimum of 1-2 years' work experience in a healthcare-related field or life sciences firm.
Salary: $70,000
Type: Full-time
Benefits: Annual discretionary performance bonus and a comprehensive benefits package.

Orchard Therapeutics

Skills & Focus: clinical trials, clinical study, administration, project support, documentation, communication, organisational skills, study trackers, CRO, finance reconciliation
About the Company: Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the develop…
Experience: 2-years CTA experience; Experience & knowledge of supporting clinical trials, particularly coordination/administration

Atalanta Therapeutics

Skills & Focus: clinical development, neurological diseases, clinical trials, regulatory submissions, medical strategy, cross-functional teams, clinical trial protocols, Good Clinical Practice (GCP), scientific communications, medical expertise
About the Company: Building on our founders’ Nobel-prize winning discoveries in RNA interference, Atalanta Therapeutics is developing novel Di-siRNA therapies to treat severe neu…
Experience: A minimum of 3 years of experience in clinical development within the biotechnology or pharmaceutical industry
Type: Full-time

Whoop

Skills & Focus: clinical research, data analysis, study design, protocol development, data integrity, statistical analysis, cross-functional teams, regulatory submissions, literature reviews, research publications
About the Company: WHOOP is an advanced health and fitness wearable on a mission to unlock human performance. WHOOP empowers its members to improve their health and perform at a …

Seaport Therapeutics

Skills & Focus: clinical studies, CRO management, Informed Consent Form, project leadership, timelines, budgets, site management, quality assurance, clinical trial communications, CNS therapeutic experience
About the Company: Seaport Therapeutics is a clinical-stage biopharmaceutical company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient…
Experience: Minimum 4+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role
Type: Hybrid

Iqvia

Skills & Focus: data management, clinical data management, project management, negotiations, quality management, financial tracking, process improvements, Good Clinical Practices, regulatory guidelines, compliance
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 5 years direct Data Management experience, including 3 or more years as a CDM project lead.
Salary: $82,300.00 - $173,900.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Veeva Systems

Skills & Focus: clinical trials, go-to-market strategies, sponsor-site interactions, contract research organizations (CROs), site collaboration, adoption, Site Connect application, efficiency, clinical operations, cross-functional team
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: Strong understanding of clinical operations and sponsor-site interactions
Type: Full-time
Benefits: Work from home or in the office

Astrazeneca

Skills & Focus: clinical research, operations management, study deliverables, project management, clinical trials, talent development, team leadership, regulatory compliance, performance metrics, stakeholder management
About the Company: AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines.
Experience: Minimum 7 years of clinical research experience

Manifold Bio

Skills & Focus: Program Management, Drug Development, Project Management, Biotechnology, Collaboration, Clinical Trials, IND Preparation, Partnerships, Project Plans, Communication
About the Company: Manifold Bio is a biotech company pursuing a pipeline of protein therapeutics using novel molecular measurement technologies and library-guided protein enginee…
Experience: Program management experience for drug development programs in late nonclinical/early clinical phases, with proven track record of advancing candidates into the clinic.

Orchard Therapeutics

Skills & Focus: clinical trials, clinical study managers, project administrative support, communication, documentation, timeline management, budget oversight, team environment, organizational skills, MSOffice
About the Company: Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the develop…
Experience: 2-years CTA experience

Costello Medical

Skills & Focus: administrative tasks, project coordination, scientific tasks, quality control, client communication, project timelines, logistics coordination, scientific documents, customer service, cross-collaboration
About the Company: Costello Medical specializes in medical communications, market access, evidence development, and rare diseases. They focus on delivering high-quality work and …
Experience: No prior industry experience required, but candidates should be proactive and eager to take on new challenges.
Salary: $58,000 - $60,000 per annum
Type: Full-time, permanent
Benefits: Hybrid working options, generous holiday allowance, flexible working hours, private medical and dental insurance, 401K …

Tango Therapeutics

Skills & Focus: clinical trials, oncology, project management, vendor management, GCP/ICH, clinical research operations, timelines, metrics, team collaboration, budget management
About the Company: Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the trea…
Experience: 12 years in clinical research operations, with at least 2 years of oncology experience required, 5+ years preferred.

Regeneron Pharmaceuticals Inc.

Skills & Focus: Oncology, Clinical Trial Management, Leadership, Clinical Research, Budget Management, Operational Insight, Risk Mitigation, Clinical Programs, Vendor Management, Team Management
Experience: Minimum of 12 years relevant industry experience, 8 years within clinical trial management.
Salary: $202,000.00 - $336,600.00
Type: Hybrid
Benefits: Health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off.
Skills & Focus: clinical operations, clinical trial management, clinical research studies, quality, timelines, budgets, staff recruitment, mentoring, operational insight, risk mitigation strategies
Experience: minimum of 12 years relevant sponsor side pharmaceutical industry experience, 8 years within clinical trial management.
Salary: $202,000.00 - $336,600.00
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees
Skills & Focus: clinical trials, study design, patient recruitment, data management, budget management, risk assessment, protocol development, team leadership, study close-out, regulatory compliance
About the Company: Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases.
Experience: 8 years relevant clinical trial experience
Salary: $148,300.00 - $241,900.00
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees

Scholar Rock

Skills & Focus: clinical trials, administrative support, documentation, research administration, drug trials, biologics, meeting minutes, metrics reporting, inspection readiness, problem-solving
About the Company: Scholar Rock is a biopharmaceutical company that discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unme…
Experience: Preferred Experience in a CRO, Sponsor or clinical research administration function, including hands on experience relating to the essential documentation of a clinical trial.
Type: Full-Time

Johnson & Johnson

Skills & Focus: Clinical Development, Neuroscience, Medical Monitoring, Regulatory Affairs, Clinical Trials, Strategic Decision Making, Cross-functional Teams, Adverse Events, Pharmaceutical Development, Patient-Focused
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: MD (or equivalent) in relevant area with appropriate post-doctoral training and certification
Salary: $194,000 - $334,650
Type: Hybrid
Benefits: Eligible for an annual performance bonus, medical, dental, vision, life insurance, short- and long-term disability.

Cullinan Therapeutics, Inc.

Skills & Focus: clinical trial, study management, administrative, oncology, autoimmune disease, biopharmaceutical, portfolio, therapeutics, research, development
About the Company: Cullinan Therapeutics, Inc. (Nasdaq: CGEM) is a biopharmaceutical company dedicated to creating new standards of care for patients. We have strategically built…

Flagship Pioneering

Skills & Focus: clinical trials, early phase, clinical development, study protocols, patient journey, proof of concept, trial execution, collaborate, innovative trials, regulatory compliance
About the Company: Flagship Pioneering conceives, creates, resources, and develops first-in-category life science platform companies to transform human health and sustainability.…

Iterative Health

Skills & Focus: clinical research finance, invoicing, accounts payable, clinical research budgets, Clinical Trials Management System, RealTime, study budgets, financial reports, GAAP principles, stakeholder communication
About the Company: Iterative Health is a healthcare technology and services company on a mission to advance gastrointestinal care through relentless innovation. With deep experti…
Experience: At least 7 years’ experience working with clinical research finance, for a research site; 5+ years experience in a strategic customer facing role
Salary: $110,000 — $130,000 USD
Type: Full-time
Benefits: Vision/Dental/Medical Insurance, Life/Disability Insurance, Parental Leave, Stock Options, Flexible Work Hours, Unlimit…

Aditum Bio

Skills & Focus: Clinical Trial Design, Clinical Trials, Phase I, Phase II, Medical Monitoring, Safety Oversight, Regulatory Requirements, Compliance, Clinical Strategy, Cross-functional Team
About the Company: At Aditum Bio our mission is to provide access to medicines to patients in need. Co-founded by industry veterans Joe Jimenez, former CEO of Novartis and Mark F…
Experience: A minimum of 6 years of industry experience in clinical development in a pharmaceutical or biotech company setting.
Salary: $335,000 - 375,000
Type: Full-time
Benefits: medical, dental, vision, and 401k

Kyowa Kirin North America

Skills & Focus: clinical operations, clinical trials, project planning, resource management, regulatory guidelines, clinical management, stakeholder management, clinical development, cross functional, CRO selection
About the Company: Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in …
Experience: Minimum 12 years of experience in study management at a sponsor/biotechnology/pharmaceutical company. Minimum 5 years demonstrated managerial, organizational, and leadership skills in a dynamic environment running multiple clinical trials.

Moma Therapeutics

Skills & Focus: clinical trial, oncology, vendor management, clinical operations, GCP/ICH, drug development, performance management, project management, study budgets, cross-functional teams
About the Company: MOMA Therapeutics is a clinical-stage, next-generation precision medicine company dedicated to targeting highly dynamic proteins that underlie human disease vi…
Experience: 8+ years of clinical research experience with at least 5 years of industry experience (pharmaceutical or biotech)
Type: 1099 Independent Consulting
Benefits: MOMAtes (full time employees) receive a highly competitive benefits package including health, dental and vision coverag…

Tessera Therapeutics

Skills & Focus: clinical operations, clinical trial management, global clinical trials, cross-functional teams, ICH/GCP guidelines, regulatory guidelines, risk management, project management, budget management, patient recruitment
About the Company: Tessera Therapeutics is pioneering Gene Writing™— a new biotechnology designed to offer scientists and clinicians the ability to write small and large therapeu…
Experience: 8+ years of clinical operations experience, including 4+ years as a clinical trial manager
Type: Full-time
Benefits: Tessera offers a competitive package of base and incentive compensation as well as a comprehensive benefits program des…

Dyne Therapeutics

Skills & Focus: Clinical Operations, clinical trials, study conduct, regulatory documents, study metrics, team collaboration, investigator meetings, trial master file, best practices, inspection readiness
About the Company: Dyne Therapeutics is discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases. Leve…
Experience: 2+ years of relevant hands-on drug development experience in Sponsor setting
Type: Full-time

Ardelyx

Skills & Focus: clinical trial, CRO, vendor management, regulatory submissions, medical terminology, clinical development, study documentation, communication skills, proficiency in MS Office, study materials
About the Company: Ardelyx is a publicly traded commercial biopharmaceutical company founded with a mission to discover, develop and commercialize innovative first-in-class medic…
Experience: 3+ years of experience in clinical trial operations
Salary: $93,000 - $113,000
Type: Full-time
Benefits: Ardelyx offers a robust benefits package including a 401(k) plan with employer match, paid parental leave, health plans…

Dyne Therapeutics

Skills & Focus: Program Management, Cross-functional team, Development plan, Clinical development, Regulatory strategy, Project execution, Stakeholder communication, Risk management, Neuromuscular diseases, Therapeutics
About the Company: Dyne Therapeutics is discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases.
Experience: 8-12+ years
Skills & Focus: clinical supply, pharmaceutical, project management, investigational medicinal product (IMP), drug development, contract manufacturing, regulatory affairs, clinical operations, quality systems, supply chain management
About the Company: Dyne Therapeutics is discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases.
Experience: Minimum of 10 years of related experience in the pharmaceutical industry with at least 5 years of direct experience in Global Clinical Supply Management.
Skills & Focus: clinical operations, clinical trials, CRO management, operation strategy, budget managing, vendor performance, data monitoring, risk assessments, clinical development, regulatory compliance
About the Company: Dyne Therapeutics is discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases. Leve…
Experience: Minimum of 8 years of clinical trial management experience

Ardelyx

Skills & Focus: clinical trial, CRO, medical terminology, ICH GCP Guidelines, regulatory submissions, study documentation, clinical studies, progress reports, MS Office, communication skills
About the Company: Ardelyx is a publicly traded commercial biopharmaceutical company founded with a mission to discover, develop and commercialize innovative first-in-class medic…
Experience: 3+ years of experience in clinical trial operations
Salary: $93,000 - $113,000
Type: Full-time
Benefits: 401(k) plan with generous employer match, 12 weeks of paid parental leave, flexible time off, health plans (medical, pr…
Skills & Focus: clinical trial management, project management, GCP, regulatory requirements, risk management, vendor relationships, EDC systems, clinical research, timelines, budgets
About the Company: Ardelyx is a publicly traded commercial biopharmaceutical company founded with a mission to discover, develop and commercialize innovative first-in-class medic…
Experience: 5+ years of experience in clinical trial management or related clinical research positions
Salary: $126,000-$154,000
Type: Full-time
Benefits: 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks of living organ and bone marr…
Skills & Focus: clinical trial management, project management, GCP, regulatory requirements, risk management, clinical sites, data analysis, vendor relationships, EDC systems, communication skills
About the Company: Ardelyx is a publicly traded commercial biopharmaceutical company founded with a mission to discover, develop and commercialize innovative first-in-class medic…
Experience: 5+ years of experience in clinical trial management or related clinical research positions
Salary: $126,000-$154,000
Type: Full-time
Benefits: 401(k) plan with generous employer match, 12 weeks of paid parental leave, equity incentive plans, health plans, life i…

Treeline Biosciences

Skills & Focus: Clinical Development Planning, Clinical Development Implementation, Clinical trial protocols, Oncology, Medical monitor, Good Clinical Practice, Biostatistics, Translational Biomarker, Regulatory interactions, Ethical conduct
About the Company: Treeline has a robust research pipeline from discovery to clinic, and we are working rigorously to leverage this for the greatest possible impact for patients.
Experience: Clinical practice experience ≄ 4 years.
Type: Full-time
Skills & Focus: clinical operations, clinical trials, study management, oncology, CRO management, regulatory compliance, project risks, study deliverables, team collaboration, data management
Experience: 5-8+ years of trial management experience as primary Clinical Trial Manager (or equivalent) within Pharma, Biotech or CRO; Oncology experience required.
Skills & Focus: Clinical Data Management, EDC systems, Regulatory guidelines, Data quality, Vendor oversight, Clinical trials, SOP creation, Biostatistics, Medical coding, Project management
About the Company: Treeline Biosciences, a clinical-stage biotechnology company, is seeking a skilled Clinical Data Leader to join our dynamic team. This role offers the opportun…
Experience: 7+ years of clinical data management experience in the pharmaceutical or biotechnology industry.
Benefits: Dynamic and innovative work environment with opportunities to contribute to groundbreaking research.