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Clinical Research Associate Jobs in Riverside, RI

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 ...

Brown University

Senior Research Associate

Providence, RI · On-site

$70 - $90/hr

Senior Research Associate Brown University, Annenberg Institute for School Reform About Brown University Brown University is a leading research university distinct for its student-centered learning ...

Brownhealth

Clinical Research Assistant

Providence, RI · On-site

$41K - $68K/yr

Under the general supervision of the Principal Investigator(s) and Clinical Research Coordinator, assist in acquisition and analysis of patient information for multiple clinical research projects.

Brownhealth

Clinical Research Assistant

Providence, RI

$41K - $68K/yr

Under the general supervision of the Principal Investigator(s) and Clinical Research Coordinator, assist in acquisition and analysis of patient information for multiple clinical research projects.

Brownhealth

Clinical Research Assistant

Providence, RI · On-site

$41K - $68K/yr

Under the general supervision of the Principal Investigator(s) and Clinical Research Coordinator, assist in acquisition and analysis of patient information for multiple clinical research projects.

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

Clinical Research Associate information

See Riverside, RI salary details

$11

$40

$68

How much do clinical research associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical research associate in Riverside, RI is $40.36, according to ZipRecruiter salary data. Most workers in this role earn between $28.32 and $51.68 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.
More about Clinical Research Associate jobs

What are the most commonly searched types of Clinical Research jobs in Riverside, RI?

The most popular types of Clinical Research jobs in Riverside, RI are:

What job categories do people searching Clinical Research Associate jobs in Riverside, RI look for?

The top searched job categories for Clinical Research Associate jobs in Riverside, RI are:

What cities near Riverside, RI are hiring for Clinical Research Associate jobs?

Cities near Riverside, RI with the most Clinical Research Associate job openings:

Clinical Research Associate jobs near you

Clinical Research Coordinator II

Panoramic Health

Providence, RI • On-site

$24.50 - $32.50/hr

Full-time

Posted 5 days ago

Job description

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 our clinical research team in Providence, Rhode Island. This role offers the opportunity to play a key part in the execution of clinical research studies while working closely with investigators, physicians, clinic staff, patients, sponsors, and the broader research team.
The CRC II will take ownership of day-to-day study coordination at the site level, with a strong focus on patient recruitment and enrollment, study execution, regulatory and protocol compliance, data quality, and patient safety. The ideal candidate is organized, proactive, and comfortable managing multiple studies and a high volume of patients while maintaining a high standard of accuracy and quality.
What You'll Do
Study Start-Up & Site Readiness
  • Read, understand, and operationalize assigned research protocols and study requirements.
  • Prescreen patients and identify potentially eligible research participants.
  • Train site staff on study purpose, procedures, and requirements; maintain appropriate training documentation.
  • Evaluate study resources and coordinate with clinic leadership to ensure the site is prepared for successful study execution.
  • Develop and implement workflows that improve recruitment, enrollment, patient flow, and study operations.

Patient Recruitment & Enrollment
  • Proactively identify and recruit potentially eligible patients through collaboration with physicians, clinic staff, and the research team.
  • Communicate study eligibility criteria and research opportunities to referring physicians and clinic staff.
  • Partner with the Central Research team, including the Central Enrollment Team, to meet or exceed referral, consent, and enrollment targets.
  • Obtain and document informed consent in accordance with ICH/GCP, protocol requirements, and site SOPs.
  • Promote a positive patient experience while prioritizing patient safety and ethical research practices.

Study Coordination & Patient Visits
  • Coordinate and plan subject visits according to protocol-specific schedules and requirements.
  • Ensure visits and procedures are completed within protocol-defined windows and minimize protocol deviations.
  • Perform basic clinical procedures, including vital signs, height, weight, blood collection, and ECGs.
  • Collect, process, and ship laboratory specimens according to protocol requirements.
  • Dispense and collect investigational product/medication and maintain accurate accountability records.
  • Monitor patient participation and maintain accurate patient tracking documentation.

Data & Documentation
  • Complete case report forms (CRFs), electronic data capture systems, and other study documentation accurately and in a timely manner.
  • Maintain data integrity in accordance with ALCOA principles: Attributable, Legible, Contemporaneous, Original, and Accurate.
  • Maintain a thorough understanding of study-specific data collection instruments and ensure data are collected according to protocol.
  • Report adverse events and serious adverse events to the appropriate IRB, sponsor, and management within required timelines.
  • Maintain accurate study files, logs, source documentation, and patient records.

Monitoring & Quality Oversight
  • Prepare for and support sponsor/CRO monitoring visits.
  • Ensure source documents are organized, complete, and readily available for monitoring.
  • Respond to monitor follow-up letters in a timely manner and ensure outstanding items are resolved.
  • Maintain current temperature logs, investigational product accountability records, and other required study documentation.
  • Resolve data queries and outstanding action items promptly.
  • Maintain compliance with study protocols, site SOPs, ICH/GCP, IATA, FDA regulations, and applicable research requirements.

Site Operations & Collaboration
  • Coordinate with location administration to ensure appropriate space, equipment, supplies, and other resources are available for study activities.
  • Build strong working relationships with physicians, clinic staff, patients, sponsors, CROs, and internal research teams.
  • Identify operational challenges and proactively implement solutions to improve study performance.
  • Perform other duties and responsibilities as assigned.

What We're Looking For
  • 3-5 years of clinical research experience, preferably in a coordinator role with increasing responsibility.
  • Bachelor's degree in a health-related field preferred.
  • Medical Assistant (MA) certification preferred.
  • Good Clinical Practice (GCP) and/or IATA certification preferred.
  • ACRP or SOCRA certification preferred.
  • Experience in CKD, nephrology, vascular access, or a related therapeutic area is a plus.
  • Bilingual English/Spanish skills preferred.
  • Strong knowledge of medical terminology and clinical research practices.
  • Working knowledge of GCP, IATA, FDA regulations, and research compliance requirements.
  • Demonstrated ability to manage multiple studies and a high volume of patients while maintaining quality and attention to detail.
  • Ability to perform basic clinical procedures, including blood draws, vital signs, height, and weight.
  • Ability to perform ECGs.
  • Excellent organizational, interpersonal, written, and verbal communication skills.
  • Highly self-motivated and proactive, with the ability to independently drive recruitment, enrollment, data quality, and study execution.
  • Strong attention to detail and commitment to patient safety and research quality.
  • Ability to multitask, prioritize competing responsibilities, and work effectively in a fast-paced clinical environment.

Why Join Us?
This is an opportunity to join a clinical research program focused on advancing care for patients with kidney disease while gaining exposure to the full spectrum of site-level research operations. The CRC II will have meaningful ownership of study execution and the opportunity to make a direct impact on patient recruitment, research quality, and the development of new treatment options for patients with kidney disease.
The Company is committed to the principles of equal employment. We are committed to complying with all federal, state, and local laws providing equal employment opportunities, and all other employment laws and regulations. It is our intent to maintain a work environment which is free of harassment, discrimination, or retaliation because of age, race, color, national origin, ancestry, religion, sex, pregnancy (including childbirth, lactation and related medical conditions), physical or mental disability, genetic information (including testing and characteristics), veteran status, uniformed servicemember status, or any other status protected by federal, state, or local laws. The company is dedicated to the fulfillment of this policy in regard to all aspects of employment, including but not limited to recruiting, hiring, placement, transfer, training, promotion, rates of pay, and other compensation, termination, and all other terms, conditions, and privileges of employment.

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