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Clinical Project Manager Jobs in Reading, MA (NOW HIRING)

QUANTERIX CORP

Project Manager

Bedford, MA · On-site

$100K - $120K/yr

Project Manager, Custom Assay Development Bedford, MA Quanterix is a global leader in ultra ... Across discovery to clinical applications, Quanterix empowers scientists and healthcare providers ...

Quanterix

Project Manager

Bedford, MA · On-site

$100K - $120K/yr

Project Manager, Custom Assay DevelopmentBedford, MAQuanterix is a global leader in ultra-sensitive ... Across discovery to clinical applications, Quanterix empowers scientists and healthcare providers ...

Verastem

Senior Clinical Trial Manager

Boston, MA · On-site

$115K - $130K/yr

General areas of responsibility include: project planning, initiation, implementation, and closure; leading and motivating a cross functional team; milestone planning and tracking; ensuring that ...

Cognito Therapeutics

Project Manager

Cambridge, MA · On-site +1

Project Manager, Office of the CEO, Cognito Therapeutics, Inc. Location: Boston, or Remote USA ... clinical stage company translating scientific findings from MIT into therapeutic approaches for ...

Cognito Therapeutics

Project Manager

Cambridge, MA · On-site

Project Manager, Office of the CEO, Cognito Therapeutics, Inc. Location: Boston, or Remote USA ... clinical stage company translating scientific findings from MIT into therapeutic approaches for ...

Relay Therapeutics

Manager, Clinical Science

Cambridge, MA · On-site

$71K - $97K/yr

You will work closely with clinical project management, regulatory affairs, clinical operations, biostatistics, data management, and medical writing to advance one or more clinical studies. You will ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · Hybrid

$120K - $150K/yr

Bachelor's degree in a scientific, healthcare, or related field, or an RN, required. 3-4 years of Clinical Trial Manager or Clinical Project Management experience, ideally supporting oncology ...

Verastem

Clinical Trial Associate

Boston, MA · On-site

$86K - $100K/yr

Coordinates cross function project team meetings with Clinical Project Manager and assists in preparation of agendas, minutes and tracking of action items. * Assists in the creation of study ...

Verastem Oncology

Clinical Trial Associate

Boston, MA · On-site

$86 - $100/hr

Manages study investigator CDAs, contract approval and purchase order creation. * Coordinates cross‑function project team meetings with Clinical Project Manager and assists in preparation of ...

Kura Oncology

CTL/Senior Clinical Trial Leader

Boston, MA · Hybrid

$162K - $194K/yr

Responsible for the planning and management of the operational aspects of clinical trials, including CRO and vendor management/oversight, ensuring project milestones and objectives are met and ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · On-site

$120K - $150K/yr

Traits we believe make a strong candidate: ● Bachelor's degree in a scientific, healthcare, or related field, or an RN, required. ● 3-4 years of Clinical Trial Manager or Clinical Project ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · On-site

$120K - $150K/yr

Traits we believe make a strong candidate: • Bachelor's degree in a scientific, healthcare, or related field, or an RN, required. • 3-4 years of Clinical Trial Manager or Clinical Project ...

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All JobsClinical Project JobsClinical Project Manager JobsClinical Project Manager Jobs in Reading, MA

Clinical Project Manager information

See Reading, MA salary details

$30

$64

$114

How much do clinical project manager jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical project manager in Reading, MA is $64.05, according to ZipRecruiter salary data. Most workers in this role earn between $44.66 and $75.10 per hour, depending on experience, location, and employer.

What does a clinical project manager do?

A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.

What does a clinical project manager do?

A Clinical Project Manager oversees the planning, execution, and completion of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They coordinate teams, manage budgets, timelines, and ensure that studies comply with regulatory standards and company protocols. Clinical Project Managers act as the main point of contact between sponsors, vendors, and clinical research sites, working to ensure that trials progress smoothly and data integrity is maintained. Their role is critical in bringing new therapies and treatments to market safely and efficiently.

What are the key skills and qualifications needed to thrive as a clinical project manager, and why are they important?

To thrive as a Clinical Project Manager, you need expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.

What are some common challenges clinical project managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.

What is the difference between Clinical Project Manager vs Clinical Research Associate?

AspectClinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMPUsually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors and sitesMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageFound in pharmaceutical, biotech, and CRO companies overseeing entire projectsPrimarily employed by CROs and sponsors to monitor trial sites

The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

How much do clinical project managers earn?

Clinical project managers typically earn between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. Compensation may also include bonuses and benefits related to project scope and complexity.
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Clinical Project Manager jobs near you
Infographic showing various Clinical Project Manager job openings in Reading, MA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $133,230 per year, or $64.1 per hour.

Project Manager

QUANTERIX CORP

Bedford, MA • On-site

$100K - $120K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 8 days ago

Job description

Project Manager, Custom Assay Development
Bedford, MA
Quanterix is a global leader in ultra-sensitive biomarker detection, enabling breakthroughs in disease research, diagnostics, and drug development. Its vision is to lead the next era of precision biomarker science to power earlier detection, better decisions, and improved human health. Its mission is to make biology measurable at its most fundamental level, delivering earlier insight when it matters most. Across discovery to clinical applications, Quanterix empowers scientists and healthcare providers to improve patients' lives through detection and understanding of disease. Its proprietary Simoa® technology delivers industry-leading sensitivity, allowing researchers to detect and quantify biomarkers in blood and other fluids at concentrations far below traditional limits. With more than 3,400 peer-reviewed publications, Quanterix has been a trusted partner to the scientific community for nearly two decades. In 2025, Quanterix acquired Akoya Biosciences, The Spatial Biology Company®, adding multiplexed tissue imaging with single-cell resolution to its portfolio. Together, the combined company offers a uniquely integrated platform that connects biology across blood and tissue-advancing precision medicine from discovery to diagnostics.
ROLE SUMMARY:
Quanterix, a leader in ultra-sensitive biomarker detection and precision health, is seeking a highly driven Project Manager, Custom Assay Development to manage and coordinate the execution of custom client projects. This role will serve as a primary point of contact for external clients and internal project teams, ensuring projects are executed on time and within scope and budget. The Project Manager will assist in early client engagement and project scoping, support contractual preparation, manage project execution and closure, and participate in invoicing procedures for revenue recognition. The ideal candidate will have experience managing biofluid and/or tissue biomarker assay development in a biotechnology, diagnostic, CRO, or life sciences environment and possess strong communication, attention to detail, and organizational skills.
WHAT YOU'LL DO:
  • Coordinate with the commercial team to evaluate early client interest and appropriate service offerings prior to the initial pre-sale call.
  • Determine the appropriate subject matter expert and facilitate the initial pre-sale meeting with the client.
  • Work with the appropriate subject matter expert to draft the Proposal or Statement of Work for the project.
  • Provide support on contractual execution logistics alongside the commercial team.
  • Lead and manage custom assay development projects across all phases, including feasibility/prototype development, optimization, validation, kit builds, and transfer to the Clinical Sample Testing team to support downstream clinical trials.
  • Develop and maintain detailed project plans, timelines, budgets, and risk assessments.
  • Serve as the primary liaison between clients/customers and internal scientific teams.
  • Facilitate project meetings, track milestones, and provide regular status updates to stakeholders and leadership.
  • Identify project risks, resource constraints, and technical challenges; develop mitigation strategies proactively.
  • Monitor project deliverables to ensure scientific integrity, timeline adherence, and customer satisfaction.
  • Contribute to process improvement initiatives to enhance operational efficiency and project execution.
  • Facilitate end-of-study closure and manage sample/material return to the client at the completion of the study.
  • Participate in the client invoice process and revenue recognition with Finance and Accounting teams.
  • Record and maintain project KPIs and lessons learned for future improvement initiatives.
BASIC QUALIFICATIONS:
  • Bachelor's degree in a scientific or related field required.
  • 3-5+ years of experience in a life science or laboratory setting, preferably in a project management role.
PREFERRED QUALIFICATIONS:
  • Strong understanding of custom assay development and clinical trial workflows; Simoa® or spatial biology experience a plus.
  • Experience supporting or partnering with Business Development in pre-sales and solution design.
  • Superior organizational skills and the ability to rapidly learn new scientific concepts.
  • Prior experience with client-facing interactions.
  • Keen attention to detail and adherence to Standard Operating Procedures.
  • Experience with Salesforce, ERP, and project management software is desirable.
EXPECTATIONS, COMPETENCIES, SKILLS & ABILITIES:
  • Onsite 5 days per week in Bedford, MA.
  • Ability to thrive in a fast-paced, ambiguous environment with competing priorities.
  • High level of ownership, accountability, and attention to detail.
  • Excellent communication skills, both written and verbal.
  • Travel requirements: Manager to confirm.
  • Physical requirements: Manager to confirm, if applicable.
WHY YOU'LL LIKE WORKING WITH US:
Our Technology:
From discovery to diagnostics, Quanterix's ultrasensitive biomarker detection is fueling breakthroughs only made possible through its unparalleled sensitivity and flexibility. Simoa® technology has delivered the gold standard for earlier biomarker detection in blood, serum or plasma, with the ability to quantify proteins that are far lower than the Level of Quantification (LoQ). Our industry-leading precision instruments, digital immunoassay technology and CLIA-certified Accelerator laboratory have supported research that advances disease understanding and management in neurology, oncology, immunology, cardiology, and infectious disease.
Akoya Biosciences, a Quanterix company, is The Spatial Biology Company®-bringing tissue context to life through high-resolution, single-cell imaging. Akoya's spatial phenotyping platforms help researchers visualize and measure how cells organize and interact within tissue to influence disease progression and therapeutic response. From discovery through clinical research, Akoya offers a full continuum of solutions, including PhenoCycler®, PhenoImager® Fusion and HT, and PhenoCode™ Panels. As part of Quanterix, Akoya complements a leading portfolio of ultra-sensitive biomarker detection technologies, together enabling a more complete view of biology and disease across both tissue and blood.
Our Commitment to Employees:
At Quanterix, our values are based on: Team, Innovation, Customer and Owner.
Team: Challenge assumptions, not the person. Respect diversity of thought and hold ourselves to lofty standards.
Innovation: Stay curious, experiment, create and change.
Customer: Prioritize and celebrate these pioneers by doing our best to deliver on commitments.
Owner: Act with high integrity and in the best interest of Quanterix. Take measured risks and learn from their success and failures.
We reward and recognize our employees by offering competitive compensation and a 401k plan with employer match, as well as competitive health, dental, and vision benefits for employees and their dependents. We also offer an unlimited vacation policy to all exempt employees, and a generous PTO policy for non-exempt employees. All employees are eligible for equity, employee stock purchase plan, a performance bonus, and 1:1 financial counseling/planning. We also offer Tuition Assistance. We have a free, state-of-the-art onsite fitness center for all employees. To keep you fueled up, we provide onsite employees free snacks and drinks every day!
DIVERSE & INCLUSIVE WORKPLACE:
Quanterix is committed to a Diverse and Inclusive workplace. We strive to recruit candidates who will bring inclusive mindsets and contribute to our values.
Quanterix is an Equal Opportunity Employer and does not discriminate based on race, national origin, gender, gender identity, sexual orientation, protected veteran status, disability, age, or other legally protected status. Quanterix will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Pay Range: $100,000 - $120,000 per year

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