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Clinical Project Associate Jobs in Boston, MA (NOW HIRING)

Integrated Resources INC

Clinical Trial Associate

Lexington, MA · On-site

$37.75 - $51.50/hr

Clinical Project Managers, Associate Directors, or Directors), in order to facilitate the management of pre- and post-approval clinical trial processes including quality review and document prep. The ...

Ora

Clinical Research Coordinator I

Andover, MA

$24.50 - $32.75/hr

Global Project Delivery *This role is a per-diem contract opportunity* Ora Values the Daily ... Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications is strongly ...

Ora

Clinical Research Coordinator I

Andover, MA

$24.50 - $32.75/hr

Global Project Delivery *This role is a per-diem contract opportunity* Ora Values the Daily ... Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications is strongly ...

Ora

Clinical Research Coordinator I

Andover, MA · On-site

$24.50 - $32.75/hr

Global Project Delivery *This role is a per-diem contract opportunity* Ora Values the Daily ... Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications is strongly ...

Verastem

Clinical Trial Associate

Boston, MA · On-site

$86K - $100K/yr

Responsible for assisting and providing support to the members of the clinical operations project team to facilitate the operational execution of the clinical trial processes in accordance with ...

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Clinical Project Associate information

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How much do clinical project associate jobs pay per hour?

As of Jul 19, 2026, the average hourly pay for clinical project associate in Boston, MA is $34.27, according to ZipRecruiter salary data. Most workers in this role earn between $22.98 and $45.19 per hour, depending on experience, location, and employer.

What is a Clinical Project Associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

What are the typical responsibilities of a Clinical Project Associate in supporting clinical trial operations?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What are the key skills and qualifications needed to thrive as a Clinical Project Associate, and why are they important?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

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

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

What are the most commonly searched types of Clinical Project jobs in Boston, MA? The most popular types of Clinical Project jobs in Boston, MA are:
What are popular job titles related to Clinical Project Associate jobs in Boston, MA? For Clinical Project Associate jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Clinical Project Associate jobs in Boston, MA look for? The top searched job categories for Clinical Project Associate jobs in Boston, MA are:
What cities near Boston, MA are hiring for Clinical Project Associate jobs? Cities near Boston, MA with the most Clinical Project Associate job openings:
Clinical Project Associate jobs near you
Clinical Project Associate

Clinical Project Associate

Relay Therapeutics

Cambridge, MA • On-site

$61K - $87K/yr

Other

Posted 20 days ago

Job description

The Opportunity:

As Clinical Project Associate, you will be accountable for providing clinical trial coordination support, along with implementing operational plans in accordance with regulatory guidelines and ICH/GCP standards.  You will be an integral member of the Relay Tx Clinical Development Operations team making key contributions to the execution of clinical trials that will translate Relay's innovative science into impactful medicines for patients.

Your Role:

  • Partner with Clinical Project Managers to support the day-to-day operations of clinical trial execution, with a focus on site start-up, study participant enrollment, clinical monitoring, GCP and protocol compliance, from the clinical sites, CROs and vendors.
  • Serve as a point of contact for CROs, vendors, investigators and clinical site staff to support trial deliverable, effective communication and strong working relationships
  • Develop ,maintain and improve study tracking tools
  • You will assist with vendor and site invoice review as well as budget management and tracking.
  • You will review and contribute to key study documents including, but not limited to, training records, regulatory packets, informed consent forms, case report forms, study oversight committee charters, and study plans.
  • Maintain version control and documentation across clinical materials.
  •  Coordinate and track trial-specific equipment and supplies, as appropriate.
  • Coordinate trial team meetings, including schedules, distribution, agendas, minutes and action items as well as actively participate in team meetings providing updates on your key responsibilities.
  • You will help to ensure the Trial Master File (TMF) is up-to-date and inspection ready.
  • You will support inspection readiness by collaborating with CROs and providing support to clinical sites to prepare for and respond to audit/inspection findings conducted by internal QA and external regulatory agencies.
  • You will actively participate in the development of department initiatives; contribute ideas to department initiatives that will make a difference to the efficiency and effectiveness of Clinical Operations.

Your Background:

  • Bachelor's degree with at least 2+ years of relevant clinical trial experience (e.g. CRO, Sponsor experience, clinical site or clinical trial vendor).
  • You are familiar with GCP and ICH Guidelines and the application to the conduct of clinical trials
  • You are a motivated self-starter who can flourish in a fast-paced small company environment.
  • You are a creative problem-solver with excellent communication and public speaking skills.
  • You are familiar with MS Office products (MS Project, Excel and Power Point)
  • You have strong interpersonal and organizational skills, with a high degree of attention to detail.
  • You are pragmatic and have the demonstrated ability to manage multiple competing tasks and demands

Estimated Salary Range: [$61,000 - $87,000].

The range provided above is based on what we believe to be a reasonable estimate for this job at the time of posting. Actual base salary will depend on a number of factors, including but not limited to, a candidate's education, experience, skills and location.

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