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Clinical Research Associate Jobs in Woonsocket, RI

Adams Clinical

Clinical Research Coordinator I

Boston, MA · On-site

$27 - $32/hr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple ...

Eight Sleep

Director of Clinical Research

Boston, MA · On-site

Reporting to the VP of R&D, you will lead a team of 10+ research associates, data scientists, and ... Own the clinical research & science organization -- lead, mentor, and grow a team of 10+ spanning ...

panoramic

Clinical Research Coordinator II

Providence, RI · On-site

$24.50 - $32.50/hr

Nephrology Associates, Inc. | Providence, RI Advance Clinical Research. Improve Kidney Care. Nephrology Associates, Inc. is seeking an experienced Clinical Research Coordinator II (CRC II) to join ...

knownwell

Clinical Research Assistant

Boston, MA · On-site

$45K - $60K/yr

The Clinical Research Assistant (CRA) plays a vital hands-on role in the execution of clinical ... High school diploma or GED required; associate or bachelor's degree in a health-related field ...

Museum of Science

Research Associate

Boston, MA · On-site

Why We Need You The Research Associate supports the Advancement team by conducting prospect research and providing insights that inform donor engagement and fundraising strategy. This role plays an ...

Stratevi

Research Associate

Boston, MA · On-site

$75K/yr

Stratevi Job Opening Research Associate Who We Are As the name 'Stratevi' suggests, we seamlessly combine Strategy and Evidence. We are a boutique firm that partners with biotechnology ...

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

The Clinical Research Coordinator (CRC) is responsible for coordinating and managing clinical trials in accordance with study protocols, Good Clinical Practice (GCP) guidelines, institutional ...

Winaxis

Clinical Research Coordinator

Boston, MA · On-site

$26.25 - $35/hr

The Clinical Research Coordinator (CRC) is responsible for coordinating and managing clinical trials in accordance with study protocols, Good Clinical Practice (GCP) guidelines, institutional ...

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All JobsClinical Research Associate JobsClinical Research Associate Jobs in Woonsocket, RI

Clinical Research Associate information

See Woonsocket, RI salary details

$11

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$66

How much do clinical research associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical research associate in Woonsocket, RI is $39.41, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $50.43 per hour, depending on experience, location, and employer.

What is a clinical research associate?

Clinical Research Associates (CRAs) are professionals responsible for monitoring and overseeing clinical trials to ensure they are conducted in accordance with regulatory guidelines, protocols, and ethical standards. They play a key role in ensuring the safety of trial participants and the integrity of collected data. CRAs often visit clinical trial sites to verify data accuracy, maintain study documentation, and provide training to site staff. Their work ensures that new drugs, treatments, or medical devices are tested rigorously before they reach the market.

What are the key skills and qualifications needed to thrive as a clinical research associate?

To thrive as a Clinical Research Associate, you need a solid background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a relevant bachelor's degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certifications like ACRP or SOCRA is typically required. Strong organizational, communication, and problem-solving skills help build effective relationships with research sites and ensure compliance. These skills are vital for maintaining the integrity of clinical trials, ensuring regulatory adherence, and advancing medical research efficiently.

What are some common challenges clinical research associates face when monitoring clinical trial sites?

Clinical Research Associates (CRAs) often encounter challenges such as ensuring protocol compliance across multiple sites, managing tight project timelines, and maintaining accurate documentation. Additionally, CRAs must effectively communicate with site staff to resolve issues and ensure data integrity, all while adhering to regulatory guidelines. Balancing frequent travel, adapting to different site environments, and handling unexpected issues such as patient recruitment delays are also typical aspects of the role.

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

AspectClinical Research AssociateClinical Trial Coordinator
CredentialsBachelor's degree, often with clinical research certificationsBachelor's degree, often with clinical research or healthcare certifications
Work EnvironmentMonitors clinical sites, reviews data, ensures complianceCoordinates trial activities, manages schedules, and communicates with sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, CROs

Both roles are essential in clinical trials, with CRAs focusing on site monitoring and compliance, while Clinical Trial Coordinators handle day-to-day trial management. They often collaborate but have distinct responsibilities within the clinical research process.

Is being a clinical research associate worth it?

A clinical research associate (CRA) monitors clinical trials to ensure compliance with protocols and regulations, often requiring strong organizational and communication skills. The role offers opportunities for career growth, competitive salaries, and work in the healthcare or pharmaceutical industries, but it can involve irregular hours and travel. Overall, it can be a rewarding career for those interested in medical research and patient safety.

Is it hard to get a clinical research associate job?

Securing a clinical research associate (CRA) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and familiarity with trial management tools can improve job prospects, but entry-level roles may be easier to obtain with relevant internships or certifications.
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Clinical Research Associate jobs near you

Clinical Research Coordinator I

Adams Clinical

Boston, MA • On-site

$27 - $32/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 25 days ago

Job description

Join Us in Shaping the Future of Clinical Research
Adams Clinical is a leading clinical trial site network committed to accelerating the development of life-changing medicines. Our mission is simple: deliver uncompromising data quality, safety, and diverse enrollment to advance healthcare. Our vision is to set the gold standard for clinical trial excellence. We believe our people make the difference. Guided by our core values-Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration-we create an environment where meaningful work drives meaningful change.
At Adams Clinical, you'll find:
  • A culture of respect, transparency, and continuous improvement
  • Opportunities for professional growth and learning
  • A team dedicated to improving lives through innovation and integrity

If you're passionate about making an impact in clinical research and want to be part of a collaborative, mission-driven organization, we'd love to have you on our team.
Overview
Adams Clinical is a rapidly growing research site network specializing focused on late phase industry-sponsored trials of novel treatments for a variety of psychiatric and neurological conditions, supporting both inpatient and outpatient studies. Adams Clinical Site Network has locations in Watertown, MA; Boston, MA; Harlem, NY; Bronx, NY; Philadelphia, PA; and Dallas, TX.
We are seeking experienced applicants for the Clinical Research Coordinator I role at our Boston location. This role is ideal for early-career coordinators with some prior research exposure, looking to develop hands-on clinical and protocol management experience.
The Clinical Research Coordinator I is responsible for supporting and performing routine clinical research activities under the guidance of a CRC II or CRC III. The CRC I may independently manage lower-complexity trials (e.g., maintenance studies, extension studies) and serves as a secondary coordinator on high-enrolling screening trials. This role represents the first step in assuming ownership and accountability in study execution.
Key Responsibilities
  • Independently coordinate low- to moderate-complexity trials, including scheduling, visit execution, and day-to-day operations.
  • Serve as secondary CRC on high-enrolling screening trials, supporting screening, enrollment, and participant follow-up.
  • Conduct participant visits per protocol, including medical/psychiatric history collection, vitals, ECGs, phlebotomy, and specimen processing, as trained.
  • Prepare and maintain study source documents, lab kits, CRFs, and visit materials.
  • Ensure accurate, ALCOA+-compliant documentation of all study procedures and maintain required logs, trackers, and regulatory files.
  • Support investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, and documentation under supervision, ensuring compliance with protocol and site SOPs.
  • Communicate with participants between visits to maintain engagement and protocol compliance.
  • Assist with sponsor communication, monitoring visit preparation, and audit readiness as appropriate.
  • Contribute to query resolution, data cleaning, and study metrics tracking to support accurate reporting and inspection readiness.
  • Support screening operations and meet enrollment expectations for assigned study tasks.
  • Prepare internal reports or summaries for review under guidance from CRC II/III.

Qualifications
  • Bachelor's degree required.
  • At least 6 months of prior clinical research experience. Experience with industry-sponsored clinical trials preferred.
  • Strong organizational skills and ability to multitask in a fast-paced environment.
  • Willingness to continue learning hands-on clinical and research skills.

Pay: $27.00 - $32.00 per hour
Benefits:
  • 401(k) matching
  • Medical, Dental &Vision insurance
  • Employee assistance program
  • Flexible spending account
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Parental leave
  • Professional development assistance

Adams Clinical is committed to being an equal opportunity and affirmative action employer. We focus on hiring and nurturing top talent. All employment decisions, including recruitment, hiring, promotion, compensation, transfer, training, discipline, and termination, are made based on the candidate's or employee's qualifications relevant to the position. These decisions are made without regard to age, sex, sexual orientation, gender identity or expression, genetic information, race, color, creed, religion, ethnicity, national origin, citizenship, disability, marital status, military status, pregnancy, or any other legally protected status.
In compliance with federal law, all individuals hired must, as a condition of employment, provide documentation verifying their identity and authorization to work in the United States and complete Form I-9 within the required timeframe. Adams Clinical participates in E-Verify to confirm employment eligibility.

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