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Clinical Operations Associate Jobs in Quincy, MA

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 ... Work closely with our clinical operations team to coordinate, track, and manage logistics in ...

Actalent

Laboratory Operations Associate

Mansfield, MA

$27 - $37/hr

Position Overview Our client is seeking a Laboratory Operations Associate to support a growing ... Experience supporting biotech, pharmaceutical, clinical, environmental, or manufacturing laboratory ...

New

Dyne Therapeutics

Senior Clinical Trial Associate

Waltham, MA · On-site

$36.25 - $49.25/hr

The Senior Clinical Trial Associate (CTA) is a key member of the Clinical Operations team responsible for supporting the successful planning, execution, oversight, and closeout of Dyne's global ...

Socket.dev

Clinical Trial Associate

Waltham, MA · On-site

$65 - $90/hr

We are seeking a Clinical Trial Associate (CTA) will work with the Clinical Study Lead and Director ... Support the Clinical Study Lead and Clinical Operations team in the day-to-day operational ...

Dyne Therapeutics

Senior Clinical Trial Associate

Waltham, MA · On-site

$36.25 - $49.25/hr

The Senior Clinical Trial Associate (CTA) is a key member of the Clinical Operations team responsible for supporting the successful planning, execution, oversight, and closeout of Dyne's global ...

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Clinical Operations Associate information

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How much do clinical operations associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical operations associate in Quincy, MA is $27.59, according to ZipRecruiter salary data. Most workers in this role earn between $18.70 and $31.83 per hour, depending on experience, location, and employer.

What is a clinical operations associate?

A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.

What are the typical responsibilities and team dynamics for a clinical operations associate?

As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

What are the key skills and qualifications needed to thrive in the clinical operations associate position, and why are they important?

To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.

What are the most commonly searched types of Clinical Operations jobs in Quincy, MA?

The most popular types of Clinical Operations jobs in Quincy, MA are:

What are popular job titles related to Clinical Operations Associate jobs in Quincy, MA?

For Clinical Operations Associate jobs in Quincy, MA, the most frequently searched job titles are:

What job categories do people searching Clinical Operations Associate jobs in Quincy, MA look for?

The top searched job categories for Clinical Operations Associate jobs in Quincy, MA are:

What cities near Quincy, MA are hiring for Clinical Operations Associate jobs?

Cities near Quincy, MA with the most Clinical Operations Associate job openings:

Clinical Operations Associate jobs near you
Infographic showing various Clinical Operations Associate job openings in Quincy, MA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $57,397 per year, or $27.6 per hour.

Clinical Trial Associate

Skyhawk Therapeutics

Waltham, MA

$75K - $140K/yr

Full-time

Re-posted 14 days ago

Job description

Clinical Trial Associate/ Senior Clinical Trial Associate

Skyhawk Therapeutics is seeking a highly motivated CTA to provide administrative and operational support to Clinical Operations. 

Responsibilities (including, but not limited to):

  • Organize, participate in, and maintain agendas and meeting minutes for all internal and cross-functional team meetings. Review external meeting minutes as required.
  • Work closely with our clinical operations team to coordinate, track, and manage logistics in support of studies (e.g. review study plans, assist with eTMF reviews).
  • Update and maintain internal trackers (e.g. central enrollment tracker, investigator engagement tracker, bioanalytical sample tracker) and implement updates into ad-hoc presentations and reports as required.
  • Maintain internal Clinical Operations study files and perform periodic reconciliations of documents to ensure all material is present and versioned correctly.
  • Create and maintain study personnel contact lists for all studies and KOLs by disease indication.
  • Assist with the review of study-related documents for clinical studies (e.g. protocol, IB, ICFs).
  • Assist with the facilitation of important external meetings (e.g. Clinical Advisory Board meetings): outreach, scheduling, execution of CDAs and contracts, travel arrangements, presentations, agendas, and minutes.
  • Assist with bioanalytical sample tracking and management of central and third-party labs (sample shipment and analysis timelines).
  • Assist with the review of central and third-party lab documents (e.g. Lab Manual, site flowcharts).
  • Assist with monitoring trip report across the program.

Requirements, Education, Experience & Skills:

  • Relevant education and training required; Bachelor's degree in administrative, science or medical areas of study is a plus.
  • At least 3-5 years of successful administrative experience in biotech/life sciences, health care or clinical study management (title commensurate with experience, with emphasis on eTMF experience)
  • Prefers to contribute as both independent, self-starter, and a collaborative team member.
  • Excellent organizational skills; prefers and can adapt to multiple priorities in a fast-paced and fluid work environment.
  • Excellent verbal and written communication skills.
  • Excellent computer skills, including Microsoft Office Suite: Calendar, Word, Excel, and PowerPoint are essential. SharePoint and SmartSheet preferred.
  • Veeva TMF working knowledge and for senior level, demonstrated knowledge of ICH-GCP, FDA and international regulatory requirements, eTMF management/oversight, and inspection readiness
  • Demonstrated multi-tasking and project management skills.

Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Trial Associate is $75,000-140,000 annually. This range reflects the minimum and maximum target for such position. Skyhawk Therapeutics will assess the appropriate level for a qualified candidate based on job-related skills, professional experience, and relevant education or training.

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