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

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 ...

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 ...

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA · On-site

$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 ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... Able to manage multiple projects independently and use varying databases and management systems.

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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 20, 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:
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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
Associate Director/Director, Clinical Operations Compliance

Associate Director/Director, Clinical Operations Compliance

Scholar Rock

Cambridge, MA • On-site

Full-time

Posted 14 days ago

Job description

Scholar Rock is a late-stage global biopharmaceutical company focused on developing and commercializing apitegromab for children and adults with spinal muscular atrophy (SMA) and other rare, severe, and debilitating neuromuscular diseases. As a global leader in myostatin biology, a field focused on proteins that regulate muscle mass, the Company is named for the visual resemblance of a scholar rock to protein structures. Our commitment to unlock fundamentally different treatment approaches is powered by broad application of a proprietary platform, which has developed novel monoclonal antibodies to modulate protein growth factors with extraordinary selectivity. Scholar Rock works every day to create new possibilities for patients through its highly innovative anti-myostatin program, including opportunities in additional rare neuromuscular diseases. Learn more at ScholarRock.com and follow @ScholarRock on X and on LinkedIn.
Summary of Position:
Scholar Rock is looking for an associate director level subject matter expert to build clinical operations compliance while upholding our core values and staying true to our mission. Reporting to the Head of Clinical Operations, the Associate Director/Director, Clinical Operations Compliance will play a key role in oversight of adherence to standard procedures and support of issue management for the clinical programs, and ensuring programs are inspection ready.
Position Responsibilities
  • Ensure consistency in the implementation of clinical project plans by providing reviews and support template development or refinement.
  • Lead initiatives, create process/ standards, and ensure consistency, communication, and change management across Clinical Operations, specifically related to SOP and work instruction creation and management, outsourcing, and compliance.
  • Partner with cross-functional team members within Regulatory, Quality, Data Sciences, Clinical Research, Pharmacovigilance, and other key cross-functional groups to support department compliance objectives.
  • Develop TMF standards and oversight in support of inspection readiness Develop or refine Standard Operating Procedures (SOPs), vendor endorsement team process, and functional builds, e.g. TMF standards.
  • Support outsourcing partnerships through issue escalation, resolution, and CAPA mediation and documentation as a support to governance oversight.
  • Provide compliance oversight of clinical operation activities (trial management, site monitoring, vendor management, TMF, data operations, IMP management, and closeout activities, etc.) for clinical trials.
  • Review key documents in conjunction with other functional area leads (e.g. protocols, SOPs, project plans, and inspection requests, etc.).
  • Serve as the Clinical Operations compliance subject matter expert for SOPs, GCP, ICH, FDA, EMA, and other applicable regulatory requirements, ensuring practical application/compliance across study teams and vendors throughput the trial lifecycle.
  • Issue escalation, documentation, and resolution in partnership with Clinical Operations and Quality Assurance business practices.
  • Ensure consistent implementation of training and learning, including responsibility for managing functional training matrices and adherence by personnel, as well as oversight of vendor training and learning processes.
  • Contribute to global clinical / regulatory submissions.
  • Responsible for assisting in inspection readiness activities, including mock and site inspections.
  • As a subject matter expert, actively educate, engage with and seek input from key stakeholders to bolster organizational effectiveness and efficiency.
  • May require travel, including international travel.
  • Flexible to support in-office days.

Candidate Requirements
  • Bachelor's Degree (scientific discipline preferred); advanced degree preferred
  • Minimum 8 years of experience in a biotech/pharmaceutical/ CRO setting; minimum 6 years of clinical operations experience; minimum 3 years in a supervisory role
  • Proven record of success supporting complex drug development trials, including inspection readiness preparation and experience with positive outcomes from inspections
  • Demonstration of effective leadership through vision for her/his team, coaching and mentoring, and organizational development
  • Highly organized, outcome oriented, self-motivated performance
  • Comfortable in a fast-paced environment with the ability to adapt to change
  • In depth knowledge and understanding of all aspects of clinical trials
  • Excellent interpersonal skills, ability to develop important relationships with key stakeholders across a variety of disciplines, good conflict management and negotiation skills
  • Ability to analyze complex issues to develop relevant and realistic plans, programs and recommendations
  • Excellent knowledge and experience with federal regulatory requirements and guidelines for Good Clinical Practice
  • Outstanding oral and written communication skills including authoring and driving the development of SOPs and other key trial documents

$175,000 - $240,000 a year
Scholar Rock is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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