Last updated: 2025-05-08

42 Clinical Operations Management jobs in Boston.

Hiring now: Clinical Trial Associate @ Orchard Th, Medical Dir @ Atalanta T, Clinical Research Scienti @ Whoop, Associate Dir Of Clinical @ Tango Ther, Clinical Research Associa @ Iqvia, Associate Regulatory Affa @ Astrazenec, Clinical Trial Mgr @ Seaport Th, Site Connect Strategist @ Veeva Syst, Associate Dir Of Program @ Manifold B, Primary Research Coordina @ Clearview .Explore more at jobswithgpt.com.

šŸ”„ Skills

clinical trials (16) project management (14) clinical operations (10) vendor management (6) clinical development (5) regulatory submissions (5) clinical trial (5) timelines (5) oncology (5) clinical trial management (5)

šŸ“ Locations

Boston (15) Cambridge (13) Waltham (9) Watertown (3) Newton (1) Somerville (1)
šŸ” Go to full job search

Orchard Therapeutics

Clinical Trial Associate (CTA) Boston
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 developā€¦
Experience: 2-years CTA experience; Experience & knowledge of supporting clinical trials, particularly coordination/administration

Atalanta Therapeutics

Medical Director Boston
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 foundersā€™ Nobel-prize winning discoveries in RNA interference, Atalanta Therapeutics is developing novel Di-siRNA therapies to treat severe neuā€¦
Experience: A minimum of 3 years of experience in clinical development within the biotechnology or pharmaceutical industry
Type: Full-time

Whoop

Clinical Research Scientist Boston
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 ā€¦

Tango Therapeutics

Associate Director of Clinical Data Management Boston
Skills & Focus: clinical data management, CROs, data handling, data management plans, database lock, clinical trials, CDASH, SDTM, vendor management, collaboration
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 treaā€¦
Experience: At least 8 years of clinical data management experience in industry.

Iqvia

Clinical Research Associate, Sponsor Dedicated Boston
Skills & Focus: monitoring, site management, Good Clinical Practice, study protocol, subject recruitment, documentation, data integrity, communication, regulatory submissions, clinical trial
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrieā€¦
Experience: Requires at least 2 years of on-site monitoring experience.
Salary: $71,900.00 - $189,000.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs.

Astrazeneca

Associate Regulatory Affairs Director Boston
Skills & Focus: Regulatory Affairs, Project Management, Regulatory Submissions, Drug Development, Cross-Functional Teams, Risk Management, Health Authorities, Documentation, Collaboration, Stakeholder Management
About the Company: AstraZeneca is one of the worldā€™s most forward-thinking and connected BioPharmaceutical companies. Their purpose is to help patients all over the world by deliā€¦
Experience: 5+ years of regulatory experience within the biopharmaceutical industry or health authority

Seaport Therapeutics

Clinical Trial Manager Boston
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 patientā€¦
Experience: Minimum 4+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role
Type: Hybrid

Iqvia

Data Team Lead Boston
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 industrieā€¦
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

Site Connect Strategist Boston
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 theā€¦
Experience: Strong understanding of clinical operations and sponsor-site interactions
Type: Full-time
Benefits: Work from home or in the office

Astrazeneca

Director, Country Operations Management Boston
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

Associate Director of Program and Alliance Management Boston
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 engineeā€¦
Experience: Program management experience for drug development programs in late nonclinical/early clinical phases, with proven track record of advancing candidates into the clinic.

Clearview Healthcare Partners

Primary Research Coordinator Boston
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, Londonā€¦
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

Clinical Trial Administrator Boston
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 developā€¦
Experience: 2-years CTA experience

Costello Medical

Project Coordinator Boston
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 ā€¦
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 ā€¦

Tango Therapeutics

Director, Clinical Operations Boston
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 treaā€¦
Experience: 12 years in clinical research operations, with at least 2 years of oncology experience required, 5+ years preferred.

Beam Therapeutics

Director of Pharmacovigilance Cambridge
Skills & Focus: pharmacovigilance, safety reports, clinical trials, signal detection, risk management, MedDRA dictionary, aggregate safety reports, electronic data capture, FDA regulations, project management
About the Company: Beam Therapeutics is committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assemblā€¦
Experience: 10+ yearsā€™ pharmaceutical industry experience, including a minimum of 5 yearsā€™ experience in pharmacovigilance (PV).

Regeneron Pharmaceuticals Inc.

Director, Program Operations Leader - Oncology Cambridge
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.

Relay Therapeutics

Quality Lead Cambridge
Skills & Focus: GCP, Quality Assurance, clinical trials, audit plans, inspection readiness, quality management system, clinical vendor evaluation, clinical development, CAPAs, drug discovery
About the Company: Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies toā€¦
Experience: Minimum of 8 years of Quality Assurance/GCP/GCLP/GVP Operations experience in pharmaceutical or biotech industry.
Type: Full-time

Regeneron Pharmaceuticals Inc.

Director, Program Operations Leader- Phase 4/RWE Cambridge
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
Director, Program Operations Leader - General Medicines/Phase 4 Cambridge
Skills & Focus: clinical trial management, leadership, strategic management, clinical operations, quality, timelines, budgets, risk mitigation, vendor management, staff recruitment
About the Company: A fully integrated biopharmaceutical company that invents life-transforming medicines for people with serious diseases.
Experience: Minimum of 12 years relevant sponsor side pharmaceutical industry experience, 8 years within clinical trial management.
Salary: $198,000.00 - $330,000.00
Type: On-site/Hybrid
Benefits: Comprehensive benefits, health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off.

Blueprint Medicines

Manager, Investigational Supply Operations Cambridge
Skills & Focus: clinical supply plans, CTM packaging, labeling, distribution, inventory management, GMP, CROs, project management, forecasting, Good Clinical Practices (GCP)
About the Company: Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solviā€¦
Experience: 3 years in the management of CTM packaging and labelling, including CTM for international studies, preferably within the pharmaceutical or biotechnology industry
Type: Full-time

Scholar Rock

Sr. Clinical Trial Assistant Cambridge
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 unmeā€¦
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

Regeneron Pharmaceuticals Inc.

Senior Manager Clinical Study Lead Cambridge
Skills & Focus: clinical trials, study design, project management, budget management, protocol development, regulatory compliance, risk assessment, vendor management, cross-functional leadership, data quality
About the Company: Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Our innovative medicines are designed tā€¦
Experience: Minimum of 8 years of relevant industry experience
Salary: $148,300.00 - $241,900.00
Type: Full-time
Benefits: Comprehensive benefits often include health and wellness programs, fitness centers, equity awards, annual bonuses, and ā€¦

Cullinan Therapeutics, Inc.

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

Iterative Health

Clinical Research Finance Manager Cambridge
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 expertiā€¦
Experience: At least 7 yearsā€™ experience working with clinical research finance, for a research site; 5+ years experience in a strategic customer facing role
Salary: $110,000 ā€” $130,000 USD
Type: Full-time
Benefits: Vision/Dental/Medical Insurance, Life/Disability Insurance, Parental Leave, Stock Options, Flexible Work Hours, Unlimitā€¦

Aditum Bio

Senior Director, Clinical Development Cambridge
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 Fā€¦
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

Director, Clinical Operations- Clinical Trial Execution Cambridge
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 ā€¦
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

Clinical Operations Consultant Cambridge
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 viā€¦
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 coveragā€¦

Parexel

Site Care Partner Newton
Skills & Focus: Clinical Trials, Site Care Partner, Functional Service Provider, CRA, Clinical Research, Operations Leader, Patient-Centric, Project Leadership, Medical Research, Regulatory Strategy
About the Company: Parexel is a global clinical research organization that provides comprehensive services to pharmaceutical, biotechnology, and medical device industries. Their ā€¦

Tessera Therapeutics

Clinical Operations Lead Somerville
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 Writingā„¢ā€” a new biotechnology designed to offer scientists and clinicians the ability to write small and large therapeuā€¦
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 desā€¦

Ardelyx

Clinical Trial Management Associate Waltham
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 medicā€¦
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 plansā€¦

Astrazeneca

Executive Director, Global Projects Leader - Strategic Regimens (Lung) Waltham
Skills & Focus: oncology, drug development, clinical trials, phase III, strategic leadership, global project management, collaboration, regulatory knowledge, lung cancer, matrix teams
About the Company: We are AstraZeneca, one of the worldā€™s most forward-thinking and connected BioPharmaceutical companies.
Experience: 10yrs or more Industry experience in drug development including experience in early phase clinical drug development and regulatory knowledge

Dyne Therapeutics

Associate Director, Clinical Operations Study Lead Waltham
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. Leveā€¦
Experience: Minimum of 8 years of clinical trial management experience
Director, Clinical Supply Waltham
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.
Vice President, Head of Clinical Operations Waltham
Skills & Focus: clinical operations, clinical trials, regulatory, vendor oversight, project management, strategic planning, budget management, performance indicators, clinical research, cross-functional collaboration
About the Company: Dyne Therapeutics is discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases.
Experience: At least 15 years of relevant clinical operations experience; or MS or PhD in a scientific discipline and 12 years of relevant clinical operations experience.

Ardelyx

Clinical Trial Management Associate Waltham
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 medicā€¦
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, prā€¦

Dyne Therapeutics

VP, Clinical and Commercial Supply Waltham
Skills & Focus: clinical supply management, project management, inventory control, logistics, commercial supply chain, biopharmaceutical development, quality assurance, regulatory requirements, supply chain processes, stakeholder engagement
About the Company: Dyne Therapeutics is discovering and advancing innovative life-transforming therapeutics for people living with genetically driven neuromuscular diseases. Leveā€¦
Experience: A minimum of 15 years of relevant biopharmaceutical CMC and/or Engineering experience

Ardelyx

Clinical Trial Manager Waltham
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 medicā€¦
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 iā€¦
Clinical Trial Manager Waltham
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 medicā€¦
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 marrā€¦

Treeline Biosciences

Clinical Data Leader Watertown
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 opportunā€¦
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.
Medical Director Watertown
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 ā‰„ 4 years.
Type: Full-time
Senior Clinical Trial Manager Watertown
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.