ZipRecruiter

Log In

1

Clinical Project Associate Jobs in Brookline, MA

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 ...

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$75K - $90K/yr

The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research projects, working with the study team in the initiation, maintenance and closeout of clinical projects ...

eGenesis

Associate Director, Clinical Science

Cambridge, MA · On-site

$175 - $226/hr

The Associate Director, Clinical Science is responsible for the planning, execution and operational ... Support the design and implementation of early and late-stage clinical projects and ensure that the ...

Icon plc

Feasibility Informatics Manager

Cambridge, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

To lead the process of clinical project feasibility during standalone feasibility (awarded ... Collecting data from data assets as well as country associates, site level Investigators, and KOL ...

RSM

Supervisor - Epic Clinical Analyst

Boston, MA

We are currently seeking anEpic Clinical Subject Manager & Project Manager to join our Healthcare ... Supervise associates and senior associates by reviewing work quality, providing coaching, assigning ...

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA

$75K - $140K/yr

Clinical Trial Associate/ Senior Clinical Trial Associate Skyhawk Therapeutics is seeking a highly ... Demonstrated multi-tasking and project management skills. Skyhawk Therapeutics is committed to pay ...

previous pagenext page

Showing results 21-40

All JobsClinical Project Associate JobsClinical Project Associate Jobs in Brookline, MA

Clinical Project Associate information

See Brookline, MA salary details

$13

$34

$59

How much do clinical project associate jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for clinical project associate in Brookline, MA is $34.12, according to ZipRecruiter salary data. Most workers in this role earn between $22.88 and $45.00 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?

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?

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 job categories do people searching Clinical Project Associate jobs in Brookline, MA look for?

The top searched job categories for Clinical Project Associate jobs in Brookline, MA are:

What cities near Brookline, MA are hiring for Clinical Project Associate jobs?

Cities near Brookline, MA with the most Clinical Project Associate job openings:

Clinical Project Associate jobs near you
Infographic showing various Clinical Project Associate job openings in Brookline, MA as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 18% Part Time, 1% Temporary, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $70,978 per year, or $34.1 per hour.

Senior Clinical Trial Associate (Sr. CTA)

MapLight Therapeutics

Burlington, MA • On-site

$115K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.
What You'll Do:
The Senior Clinical Trial Associate (Sr. CTA) is required to help support Clinical Operations and project teams. The position offers much responsibility and the opportunity to be involved in all phases of the clinical project. The position requires adaptability and the capacity to 'own' tasks, problem solve and to see activities through to their end.
Responsibilities:
  • Interact directly with Clinical (e.g., CRAs, trial managers), site staff, vendors (U.S. and worldwide, as necessary), to provide support in project-specific tasks and the overall management of clinical trials
  • Directly support under the guidance of Operational Leaders, Clinical Leaders, and Clinical Trial Managers. Specific responsibilities include:
    • Maintain and manage requests for access to and deactivation of study systems users.
    • Coordinates materials (PowerPoint presentations, templates, outstanding essential document listing, etc.) as needed for internal and external meetings, including requests for materials from external consultants, suppliers, etc.
    • Distribute safety alerts and relevant documents, if required
    • Maintain and update study team and vendor contact information
    • Assist in the planning, organizing and execution of study-specific meetings and write and distribute agendas, minutes and regular updates
    • May participate in reviewing, formatting and finalizing study-related templates, plans and manuals
    • Assist with maintaining clinical trial insurance
    • Assist with questions, issues or requests from the Clinical Research Organization (CRO)/study team and route to the appropriate individual within the organization for resolution
    • May participate in clinical data review, as required
  • Responsible for the completeness of documents managed in the Trial Master Files (TMF); performs ongoing reviews of TMF to assure quality of the documentation files and compliance with SOPs and ICH GCP Guidelines
  • Route, track and file Clinical documents. May conduct initial/ongoing review of site Clinical regulatory documentation to confirm completeness/track dates and distribute to appropriate team members for review
  • Develop and maintain study-related trackers that will support Clinical Operations and individual studies. May analyze or update data associated with the trackers
  • Other duties as assigned to support Study Team Leads and Operational Team Leads

Qualifications:
  • Bachelor's degree in a relevant subject area is highly recommended or a combination of education and applicable job experience may be considered.
  • Minimum 2+ years in the biotech /pharmaceutical industry /clinical trial management area
  • Competency of the drug development process with knowledge of ICH-GCP is a plus
  • Strong interpersonal, organizational and planning skills along with excellent verbal and written communication skills
  • Proactive and self-starter with the ability to take responsibility for tasks and execute seamlessly. Be able to identify areas for efficiency across studies in the spaces that the position is responsible for.

Travel:
  • Ability to travel up to 35%

Location: 3 day hybrid in office in Burlington, MA
Maplight is anticipating two Ph2 readouts in Q3 2026
MapLight does not accept unsolicited resumes from recruiters, staffing agencies, or search firms.
Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD&D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.
Salary Range
$115,000-$130,000 USD
EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

Apply