Clinical Research Assistant Jobs in Cambridge, MA
Clinical Research Assistant jobs in Cambridge are concentrated in Kendall Square, East Cambridge, and the Alewife corridor, across academic medical centers, biopharmaceutical firms, and clinical-stage biotechs. Employers hiring right now include Sanofi, Iterative Health, and Bristol Myers Squibb. See the openings below and apply to the ones that match your experience.
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Showing 5 of 128+ Clinical Research Assistant jobs
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
As the Project Manager, Clinical Research – New Site Build at Iterative Health for the Cardiology service line, you will lead the end-to-end execution of opening new Cardiology research sites from the ground up.
Reporting to the VP, Growth, you will serve as the central project leader responsible for coordinating every aspect of a new site's development—from site selection and facility readiness through regulatory activation, staffing, technology implementation, and study launch. Working cross functionally you'll ensure each site is delivered on time, on budget, and fully prepared to enroll patients.
This role is ideal for an experienced project manager who enjoys building new programs, thrives in highly cross-functional environments, and is passionate about expanding patient access to innovative cardiovascular clinical trials.
Where You'll Drive Impact
- Lead the end-to-end project management of de novo Cardiology clinical research site development, from approval through operational launch.
- Develop and manage comprehensive project plans, timelines, milestones, budgets, and risk registers for each new site.
- Coordinate cross-functional workstreams across Clinical Operations, Regulatory, Legal, Finance, Real Estate, Facilities, IT, HR, Procurement, and Business Development.
- Partner with Real Estate and Facilities teams to ensure new sites are designed, built, and equipped to support high-quality clinical research operations.
- Oversee site activation activities including licensing, regulatory readiness, technology implementation, equipment procurement, SOP deployment, and operational workflows.
- Coordinate recruiting timelines and onboarding activities with Human Resources to ensure appropriate staffing prior to site launch.
- Partner with Clinical Operations leadership to establish study startup readiness, investigator onboarding, and research staff training.
- Identify project risks, dependencies, and operational challenges while proactively developing mitigation plans to maintain timelines.
- Facilitate regular cross-functional project meetings and provide executive-level status updates to leadership.
- Develop standardized playbooks, templates, and project management tools to support scalable expansion across future de novo sites.
- Monitor project budgets, resource allocation, and vendor performance throughout the site development lifecycle.
- Support continuous process improvement initiatives to enhance speed, consistency, and quality of future site launches.
- Perform other duties as assigned.
What You Bring to the Team
- Bachelor's degree in Healthcare Administration, Life Sciences, Business, Project Management, or a related field.
- 5–8+ years of project management experience within healthcare, clinical research, life sciences, healthcare operations, or healthcare facility development.
- Experience leading large, cross-functional initiatives involving multiple stakeholders and competing priorities.
- Strong organizational and project management skills with exceptional attention to detail.
- Proven ability to manage multiple complex projects simultaneously while meeting aggressive timelines.
- Excellent communication, presentation, and stakeholder management skills.
- Experience developing project plans, tracking milestones, managing budgets, and reporting project performance.
- Ability to influence cross-functional teams without direct authority.
- Highly adaptable with strong problem-solving and decision-making skills.
- Comfortable working in a fast-paced, rapidly growing organization.
Preferred Qualifications
- Experience launching new healthcare facilities, physician practices, ambulatory care centers, or clinical research sites.
- Experience within Cardiology clinical research or cardiovascular healthcare.
- Knowledge of clinical trial startup, GCP, FDA regulations, and site activation processes.
- PMP certification or equivalent project management certification.
- Experience with Smartsheet, Monday.com, Asana, Microsoft Project, or similar project management platforms.
- Familiarity with CTMS, eRegulatory systems, and clinical research technologies.
How We Work
- Collaborative and low-ego team environment
- High ownership and accountability culture
- Fast-paced and highly iterative growth environment
- Open communication and continuous learning mindset
- Mission-driven organization focused on improving patient outcomes
- Comfortable navigating evolving business priorities and opportunities
Benefits That Support You
We believe great teams do their best work when they feel supported — professionally and personally.
- Hybrid work environment with in-office collaboration two days per week in either our NYC or Boston office
- Comprehensive medical, dental, and vision coverage, with up to 80% of premiums covered by Iterative Health
- Mental health and wellness support through Spring Health
- Health HSA or FSA options, and commuter FSA contributions supported by Iterative Health
- Unlimited PTO, 12 company holidays, and a company-wide shutdown between Christmas and New Years
- 401(k) program with a company match of up to 3% (up to $3,000 annually)
- Weekly in-office lunch benefit every Tuesday
- 100% company-paid short-term and long-term disability coverage
- Annual wellness and professional development stipend to support your health and growth
- And more!
At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
As the Project Manager, Clinical Research – New Site Build at Iterative Health for the Cardiology service line, you will lead the end-to-end execution of opening new Cardiology research sites from the ground up.
Reporting to the VP, Growth, you will serve as the central project leader responsible for coordinating every aspect of a new site's development—from site selection and facility readiness through regulatory activation, staffing, technology implementation, and study launch. Working cross functionally you'll ensure each site is delivered on time, on budget, and fully prepared to enroll patients.
This role is ideal for an experienced project manager who enjoys building new programs, thrives in highly cross-functional environments, and is passionate about expanding patient access to innovative cardiovascular clinical trials.
Where You'll Drive Impact
- Lead the end-to-end project management of de novo Cardiology clinical research site development, from approval through operational launch.
- Develop and manage comprehensive project plans, timelines, milestones, budgets, and risk registers for each new site.
- Coordinate cross-functional workstreams across Clinical Operations, Regulatory, Legal, Finance, Real Estate, Facilities, IT, HR, Procurement, and Business Development.
- Partner with Real Estate and Facilities teams to ensure new sites are designed, built, and equipped to support high-quality clinical research operations.
- Oversee site activation activities including licensing, regulatory readiness, technology implementation, equipment procurement, SOP deployment, and operational workflows.
- Coordinate recruiting timelines and onboarding activities with Human Resources to ensure appropriate staffing prior to site launch.
- Partner with Clinical Operations leadership to establish study startup readiness, investigator onboarding, and research staff training.
- Identify project risks, dependencies, and operational challenges while proactively developing mitigation plans to maintain timelines.
- Facilitate regular cross-functional project meetings and provide executive-level status updates to leadership.
- Develop standardized playbooks, templates, and project management tools to support scalable expansion across future de novo sites.
- Monitor project budgets, resource allocation, and vendor performance throughout the site development lifecycle.
- Support continuous process improvement initiatives to enhance speed, consistency, and quality of future site launches.
- Perform other duties as assigned.
What You Bring to the Team
- Bachelor's degree in Healthcare Administration, Life Sciences, Business, Project Management, or a related field.
- 5–8+ years of project management experience within healthcare, clinical research, life sciences, healthcare operations, or healthcare facility development.
- Experience leading large, cross-functional initiatives involving multiple stakeholders and competing priorities.
- Strong organizational and project management skills with exceptional attention to detail.
- Proven ability to manage multiple complex projects simultaneously while meeting aggressive timelines.
- Excellent communication, presentation, and stakeholder management skills.
- Experience developing project plans, tracking milestones, managing budgets, and reporting project performance.
- Ability to influence cross-functional teams without direct authority.
- Highly adaptable with strong problem-solving and decision-making skills.
- Comfortable working in a fast-paced, rapidly growing organization.
Preferred Qualifications
- Experience launching new healthcare facilities, physician practices, ambulatory care centers, or clinical research sites.
- Experience within Cardiology clinical research or cardiovascular healthcare.
- Knowledge of clinical trial startup, GCP, FDA regulations, and site activation processes.
- PMP certification or equivalent project management certification.
- Experience with Smartsheet, Monday.com, Asana, Microsoft Project, or similar project management platforms.
- Familiarity with CTMS, eRegulatory systems, and clinical research technologies.
How We Work
- Collaborative and low-ego team environment
- High ownership and accountability culture
- Fast-paced and highly iterative growth environment
- Open communication and continuous learning mindset
- Mission-driven organization focused on improving patient outcomes
- Comfortable navigating evolving business priorities and opportunities
Benefits That Support You
We believe great teams do their best work when they feel supported — professionally and personally.
- Hybrid work environment with in-office collaboration two days per week in either our NYC or Boston office
- Comprehensive medical, dental, and vision coverage, with up to 80% of premiums covered by Iterative Health
- Mental health and wellness support through Spring Health
- Health HSA or FSA options, and commuter FSA contributions supported by Iterative Health
- Unlimited PTO, 12 company holidays, and a company-wide shutdown between Christmas and New Years
- 401(k) program with a company match of up to 3% (up to $3,000 annually)
- Weekly in-office lunch benefit every Tuesday
- 100% company-paid short-term and long-term disability coverage
- Annual wellness and professional development stipend to support your health and growth
- And more!
At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.
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Find JobsClinical Research Assistant Job Market in Cambridge
Who's Hiring
- Sanofi38
- Iterative Health26
- Bristol Myers Squibb26
- Alnylam13
- EGENESIS13
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Science & Research
Clinical Research Assistant Jobs in Cambridge: Frequently Asked Questions
How do I get a clinical research assistant job in Cambridge?
Focus your search on Kendall Square and East Cambridge, where the highest concentration of clinical-stage biotechs, contract research organizations, and academic medical affiliates hire for these roles. Candidates with GCP certification, phlebotomy experience, or prior study coordination work stand out in this market. Targeting sponsors of Phase I and Phase II trials gives you the best shot at entry and growth.
Which companies hire clinical research assistants in Cambridge?
Employers hiring clinical research assistants in Cambridge right now include Sanofi, Iterative Health, and Bristol Myers Squibb, based on current listings on Migrate Mate as of August 2026. Cambridge's employer mix leans heavily toward biotech startups and mid-size clinical-stage companies alongside established academic health systems.
Are there remote clinical research assistant jobs in Cambridge?
Yes, though most clinical research assistant roles involve on-site patient interaction or laboratory work that limits full remote options. About 83% of clinical research assistant openings tied to Cambridge are remote or hybrid as of August 2026, concentrated among data-focused positions. Roles centered on regulatory documentation, data entry, and protocol tracking are the most likely to offer hybrid flexibility in Cambridge.
How can I get a clinical research assistant job in Cambridge with little or no experience?
The most realistic entry path in Cambridge is through research coordinator or clinical operations internship programs at the area's academic medical affiliates and early-phase biotech companies clustered around Kendall Square. Entry-level study coordinator and data abstractor roles at contract research organizations frequently hire candidates with a life sciences degree and no prior clinical experience. Volunteering or completing a practicum at a Cambridge-area teaching hospital strengthens your application considerably.
Which industries hire the most clinical research assistants in Cambridge?
The sectors hiring the most clinical research assistants in Cambridge are Biotechnology & Pharmaceuticals and Science & Research, based on current listings on Migrate Mate as of August 2026. Cambridge's dense cluster of clinical-stage biotechs, academic research hospitals, and contract research organizations makes it one of the most active markets for this role in the country.
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