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Clinical Operations Associate Jobs in Rhode Island

Pharmaron

Manufacturing Associate

Coventry, RI

$25 - $29/hr

Production of API's and related operations. * Safely operate all equipment according to procedure ... clinical development process across multiple therapeutic modalities, including small molecules ...

Pharmaron

Manufacturing Associate

Coventry, RI · On-site

$25 - $29/hr

Production of API's and related operations. * Safely operate all equipment according to procedure ... clinical development process across multiple therapeutic modalities, including small molecules ...

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All JobsClinical Operations Associate JobsClinical Operations Associate Jobs in Rhode Island

Clinical Operations Associate information

See Rhode Island salary details

$11

$25

$52

How much do clinical operations associate jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for clinical operations associate in Rhode Island is $25.70, according to ZipRecruiter salary data. Most workers in this role earn between $17.40 and $29.66 per hour, depending on experience, location, and employer.

What is a Clinical Operations Associate job?

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 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 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 most commonly searched types of Clinical Operations jobs in Rhode Island? The most popular types of Clinical Operations jobs in Rhode Island are:
What are popular job titles related to Clinical Operations Associate jobs in Rhode Island? For Clinical Operations Associate jobs in Rhode Island, the most frequently searched job titles are:
What job categories do people searching Clinical Operations Associate jobs in Rhode Island look for? The top searched job categories for Clinical Operations Associate jobs in Rhode Island are:
Clinical Operations Associate jobs near you
EMR Informaticist

EMR Informaticist

The Tri-Com Consulting Group

Providence, RI • On-site

Other

Posted 27 days ago

Job description

The Tri-Com Consulting Group
A Full Service IT Employment Consulting Firm is seeking qualified candidates for the following opening:

EMR Informaticist

Clinical Informaticist will support the implementation, configuration, optimization, and ongoing support of the hospital s electronic health record (EHR). This position serves as a liaison between clinical staff and information technology personnel to help ensure that EHR functionality supports clinical workflows, regulatory requirements, and high-quality patient care.

Key Responsibilities

  • Support the implementation, configuration, maintenance, and ongoing optimization of the hospital s EHR across multiple clinical domains
  • Analyze clinical and operational workflows and translate end-user needs into system functionality, configuration requirements, and process improvements
  • Design, build, and maintain clinical documentation tools (e.g., templates, order sets, and clinical decision support) aligned with clinical standards and regulatory requirements.
  • Participate in system testing activities, including unit testing, user acceptance testing, go-live readiness, and post-implementation optimization.
  • Identify opportunities to improve efficiency, data quality, and patient care outcomes through workflow redesign and system optimization and providing training and guidance to clinical staff to promote EHR adoption and effective use of the system

Requirements

  • Associate or bachelor s degree in clinical discipline, Computer Science, Informatics, or a closely related field, required.
  • A minimum of three (3) years of experience working in a hospital or healthcare environment, gained through direct clinical practice or clinical informatics, health IT, or clinical systems support roles.
  • Experience working with EHR platforms such as WellSky, Epic, Cerner, Meditech, or other enterprise healthcare systems.
  • Direct clinical practice experience (e.g., nursing, laboratory, pharmacy, radiology), preferred but not required.
  • Certification or advanced education in health or clinical informatics is preferred and may substitute for clinical experience.
  • Demonstrate knowledge of clinical workflows and healthcare operations.
  • Familiarity with clinical device integration workflows (e.g., IV pumps, bedside monitoring devices) and their interaction with the EHR, including supporting clinical workflows, documentation, and issue triage in collaboration with technical teams.

~Tri-Com is an Affirmative Action/Equal Opportunity Employer~

We strongly encourage the applications of women,

minorities, persons with disabilities, and military veterans.

As a condition of employment you will be required to pass a drug screening and other background checks including past employment and confirmation of technical certifications.

Apply