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Clinical Study Associate Jobs in Massachusetts (NOW HIRING)

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA · On-site

$75K - $140K/yr

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 ...

idexcel

Clinical Research Associate I

Marlborough, MA

$29.72/hr

Clinical Research Associate I 12/19/2016 to 04/28/2017 Marlborough, MA, USA, 01752 $29.72/HR on w2 ... The position arranges and coordinates clinical study start up activities and plays a key role in ...

idexcel

Clinical Research Associate I

Marlborough, MA

$29.72/hr

Clinical Research Associate I 12/19/2016 to 04/28/2017 Marlborough, MA, USA, 01752 $29.72/HR on w2 ... The position arranges and coordinates clinical study start up activities and plays a key role in ...

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Showing results 21-40

All JobsClinical Study Associate JobsClinical Study Associate Jobs in Massachusetts

Clinical Study Associate information

See Massachusetts salary details

$13

$34

$60

How much do clinical study associate jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical study associate in Massachusetts is $34.45, according to ZipRecruiter salary data. Most workers in this role earn between $23.12 and $45.43 per hour, depending on experience, location, and employer.

What is a clinical study associate?

Clinical Study Associates (CSAs) are professionals who support the planning, execution, and monitoring of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They help coordinate study logistics, maintain study documentation, and ensure compliance with regulatory requirements. CSAs often work closely with Clinical Research Associates, study coordinators, and investigators to ensure that trials are conducted according to protocol and timelines. Their role is essential in ensuring the accuracy and integrity of data collected during clinical research.

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

AspectClinical Study AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or CCRA beneficialBachelor's degree in health sciences or related field; certifications like CCRP advantageous
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, clinics, research centers
Job FocusMonitoring clinical trials, ensuring protocol compliance, data accuracyManaging daily trial activities, patient recruitment, data collection
Employer & Industry UsageCommonly employed in pharma and CROsPrimarily in healthcare and academic research settings

Both roles involve clinical trial oversight but differ in focus: Clinical Study Associates primarily monitor and ensure compliance during trials, while Clinical Research Coordinators manage daily trial operations and patient interactions. Understanding these distinctions helps in choosing the right career path or job search focus.

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

To thrive as a Clinical Study Associate, you need a strong understanding of clinical research processes, regulatory requirements, and typically a life sciences degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Attention to detail, organizational skills, and effective communication set top performers apart in this role. These competencies ensure accurate study documentation, regulatory compliance, and smooth coordination across research teams.

What are some common challenges clinical study associates face when managing multiple clinical trials simultaneously?

Clinical Study Associates often juggle several clinical trials at once, which can present challenges such as prioritizing competing deadlines, maintaining accurate documentation for each study, and ensuring consistent communication with cross-functional teams. Staying organized and proactive is essential, as unforeseen protocol amendments or site issues can arise. Building strong relationships with site staff and utilizing effective project management tools can help CSAs navigate these complexities and deliver high-quality results.
What are the most commonly searched types of Clinical Study jobs in Massachusetts? The most popular types of Clinical Study jobs in Massachusetts are:
What cities in Massachusetts are hiring for Clinical Study Associate jobs? Cities in Massachusetts with the most Clinical Study Associate job openings:
Clinical Study Associate jobs near you
Infographic showing various Clinical Study Associate job openings in Massachusetts as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $71,647 per year, or $34.4 per hour.

Clinical Research Associate

Integrated Resources INC

Lexington, MA

Full-time

Re-posted 11 hours ago

Job description

Company Description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

         The in-house Clinical Research Associate (CRA) is responsible for providing support for day to day clinical study activities under general supervision of the the Clinical Project Manager(s). 

         The CRA also provides support for existing departmental tasks and may take on developmental tasks as appropriate upon discussions with manager. 

         The CRA performs work within established protocols under general supervision.

         Assists the study team(s) to deliver the clinical study within agreed timelines.

         Assists in authoring/contributing to clinical study documents and study related plans developed by Clinical CROs and vendors. (E.g. Clinical Trial Insurance, IWRS specs, Lab Manual, Licensing Agreements etc.) Provides oversight of Clinical CRO Investigator background checks.

         Assists in oversight of vendor shipment of clinical supplies (e.g. lab kits, test machines, equipment etc.) being sent to sites prior to initiation as necessary.

         Provides oversight of Essential Documents for Investigational Medicine Release as per relevant SOP.

         Reviews Clinical Monitoring Reports and correspondence related to restudy and Initiation Visits and follows up with Clinical CRO to resolve open action items.

         Manages escalation of study related issues and communicates as appropriate with Clinical Project Manager.

         Responsible for the operational oversight of the Clinical CRO with regards to data feed setup in the Clinical Trial Management System.

         Assists and/or participates in planning and conduct of Investigator's Meetings as necessary.

         Assists Clinical Project Manager in tracking study related activities which are not appropriate to be outsourced.

         Reviews a percentage of monitoring visit reports for oversight and escalates issues to Clinical Project Manager.

         Assists with agenda distribution & minute taking for internal clinical study team meetings where formal documentation is needed and the Clinical CRO is not present.

         Provides oversight of Clinical CRO activities regarding amendments to confidentiality and site agreements.

         Assists study team with preparation for audits/inspections Reviews clinical close out monitoring visit reports for oversight and escalates issues to the Clinical Project Manager.

         Liaises with Transparency group to ensure Clintrials.gov is updated.

Additional Information

Feel free to forward my email to your friends/colleagues who might be available.

Thanks,

Warm Regards,

Kavita Kumari


Integrated Resources, Inc.

Direct: (732) - 844 8725

Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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