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Entry Level Clinical Research Associate Jobs in Worcester, MA

Alira Health

Clinical Research Associate

Framingham, MA · On-site

Summary ROLE The Clinical Research Associate is an important member of the Alira Health Clinical team. CRAs are highly motivated and function independently to conduct site monitoring responsibilities ...

Alira Health

Clinical Research Associate

Framingham, MA · On-site

Summary ROLE The Clinical Research Associate is an important member of the Alira Health Clinical team. CRAs are highly motivated and function independently to conduct site monitoring responsibilities ...

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 BACHELORS DEGREE REQUIRED. MUST HAVE RELEVANT 2 YEARS WORK EXPERIENCE OF CLINICAL RESEARCH.. Will be ...

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 BACHELORS DEGREE REQUIRED. MUST HAVE RELEVANT 2 YEARS WORK EXPERIENCE OF CLINICAL RESEARCH.. Will be ...

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 ... At least 2 years of experience in the clinical research/pharmaceutical/biotech arena and an ...

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 ... At least 2 years of experience in the clinical research/pharmaceutical/biotech arena and an ...

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Entry Level Clinical Research Associate information

See Worcester, MA salary details

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How much do entry level clinical research associate jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for entry level clinical research associate in Worcester, MA is $29.22, according to ZipRecruiter salary data. Most workers in this role earn between $18.70 and $33.95 per hour, depending on experience, location, and employer.

What is an entry level clinical research associate?

An Entry Level Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements, ethical guidelines, and study protocols. They assist in site selection, data collection, and verifying that study procedures are properly followed. Entry-level CRAs typically work under the supervision of senior CRAs and may travel to different clinical sites. Strong attention to detail, knowledge of Good Clinical Practice (GCP) guidelines, and organizational skills are essential. This role is a starting point for a career in clinical research, with opportunities for growth into senior CRA or project management positions.

What are the typical daily responsibilities of an entry level clinical research associate?

As an Entry Level Clinical Research Associate, your day-to-day work generally involves assisting with monitoring clinical trial sites, reviewing study documentation, and ensuring adherence to protocol and regulatory requirements. You may support more senior team members in conducting on-site or remote visits, tracking patient recruitment, and managing data collection. Additionally, you’ll communicate regularly with site staff and other stakeholders to resolve issues and ensure data quality. This hands-on experience is essential for building expertise in clinical research processes and advancing toward more senior CRA roles.

What are the key skills and qualifications needed to thrive as an entry level clinical research associate?

To thrive as an Entry Level Clinical Research Associate, you typically need a bachelor's degree in life sciences or a related field, a solid understanding of clinical trial protocols, and attention to detail. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory documentation is often required. Strong communication, organization, and problem-solving abilities help you effectively collaborate with study sites and team members. These skills are critical to ensure the accuracy, compliance, and successful progression of clinical studies.

What are the most commonly searched types of Entry Level Clinical Research jobs in Worcester, MA?

The most popular types of Entry Level Clinical Research jobs in Worcester, MA are:

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For Entry Level Clinical Research Associate jobs in Worcester, MA, the most frequently searched job titles are:

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Entry Level Clinical Research Associate jobs near you
Infographic showing various Entry Level Clinical Research Associate job openings in Worcester, MA as of August 2026, with employment types broken down into 50% Full Time, 36% Part Time, and 14% Contract. Highlights an 100% In-person job distribution, with an average salary of $60,769 per year, or $29.2 per hour.

Clinical Research Associate

Framingham, MA • On-site

Alira Health
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Alira Healthexternal

Full-time

Re-posted 16 days ago

Job description

Join our global team dedicated to innovation and initiative, where physical walls and different time zones don't limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.
Job Description Summary
Job Description
ROLE
The Clinical Research Associate is an important member of the Alira Health Clinical team. CRAs are highly motivated and function independently to conduct site monitoring responsibilities for clinical trials. CRAs work closely with the In-house CRAs, Lead CRAs, Director of Clinical Monitoring and Project Managers to ensure sites' protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues.
KEY RESPONSABILITIES
  • Performs qualification, initiation, interim, and close-out visits and ensures proper documentation of site visits.
  • Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status.
  • Facilitates adverse event reporting and ensures the reconciliation of SAE reports with source documentation and CRFs.
  • Ensures integrity of CRF data through meticulous and thorough source document review and verification.
  • Conducts investigational product accountability.
  • Reviews regulatory binder for required documents.
  • Works closely with in-house CRAs and data management to resolve queries on discrepant data.
  • Proactively identifies site issues and develops problem-solving strategies for sites.
  • Maintains regular contact with study sites to ensure protocol/GCP compliance, assesses patient accrual rates, and responds to sponsor requests.
  • Conducts audit preparation at study sites as needed.
  • Works with other CRAs to maintain consistency and promote a collaborative team atmosphere.
  • Manages and resolves conflicting priorities to deliver on commitments.
  • Complies with ICH GCP guidelines, FDA regulations, and company SOPs.
  • Participates in industry and client meetings.
  • Performs additional duties as assigned.

DESIRED QUALIFICATION & EXPERIENCE
  • BS/BA from an undergraduate program or equivalent experience
  • 2 years of clinical research experience

TECHNICAL COMPETENCES & SOFT SKILLS
  • Ability to travel.
  • Proven ability to be careful, thorough, and detail-oriented.
  • Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment.
  • Self-starter who thrives in a collaborative, yet less structured team environment
  • Ability to problem-solve unstructured or ambiguous challenges.
  • Strong command of English, both written and verbal.
  • Excellent communication and interpersonal skills with customer service orientation.
  • Proficient with MS Office Suite, particularly Word and Excel.
  • Permanent authorization to work in the country where you are applying.

Languages
English
Education
Bachelor of Science (BS): Biology, Bachelor of Science (BS): Life Sciences
Contract Type
Regular

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