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Clinical Research Director Jobs in Riverside, RI

Research Project Dir

Providence, RI · On-site

$55K - $91K/yr

Under general supervision of the Research Program Manager and the Director of the Center for ... Organization and assistance with the implementation of clinical protocols of the project and ...

Research Student PD

Providence, RI · On-site

$18 - $25.82/hr

For Clinical Research Programs: Conducts research protocols in conjunction with project staff ... All work should be under direct supervision of senior faculty member or designee.SUPERVISORY ...

Research Student PD

Providence, RI · On-site

$18 - $25.82/hr

... For Clinical Research Programs: Conducts research protocols in conjunction with project staff ... All work should be under direct supervision of a senior faculty member or designee. SUPERVISORY ...

Showing results 21-40

Clinical Research Director information

See Riverside, RI salary details

$10

$53

$114

How much do clinical research director jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical research director in Riverside, RI is $53.33, according to ZipRecruiter salary data. Most workers in this role earn between $31.83 and $70.29 per hour, depending on experience, location, and employer.

What does a clinical research director do?

A clinical research director manages medical or pharmaceutical research projects. In this role, you may oversee a research department at a university or medical facility. Your specific job duties vary, depending on the type of project you work on, but your general responsibilities include overseeing the planning stages of each research project or clinical trial, discussing outcomes and expectations with researchers, making sure that research staff members provide the proper care to participants in the trial or research project, and ensuring that data is documented properly. Clinical research directors also hire and train new staff members and check that the project follows all governmental and industry guidelines.

What are the responsibilities of a clinical research director?

A Clinical Research Director oversees the planning, coordination, and management of clinical trials and research projects within healthcare or pharmaceutical organizations. They ensure studies comply with regulatory requirements, establish research protocols, manage budgets, and supervise research teams. Additionally, they collaborate with stakeholders, analyze data, and ensure that clinical trials are conducted ethically and efficiently to advance medical knowledge and patient care.

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

To thrive as a Clinical Research Director, you need advanced knowledge of clinical trial design, regulatory compliance, and data analysis, typically supported by a medical, pharmaceutical, or life sciences degree along with significant experience in clinical research. Expertise in systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and familiarity with GCP, FDA, and ICH guidelines are essential, and certifications like CCRP or CCRA are highly valued. Leadership, strategic thinking, and strong communication skills distinguish top performers by enabling effective team management and stakeholder engagement. These competencies ensure that clinical trials are conducted ethically, efficiently, and in compliance with all regulatory standards, driving successful research outcomes.

What are some of the main challenges a clinical research director faces when overseeing multiple clinical trials simultaneously?

One of the primary challenges for a Clinical Research Director managing multiple trials is ensuring consistent protocol adherence across diverse study sites while maintaining strict regulatory compliance. Balancing resource allocation, addressing unforeseen issues such as patient recruitment delays, and effectively communicating with cross-functional teams also require strong organizational and leadership skills. Additionally, the director must stay updated on evolving industry standards and regulatory requirements to mitigate risks and ensure the integrity of all ongoing studies.

What is the difference between Clinical Research Director vs Clinical Research Manager?

AspectClinical Research DirectorClinical Research Manager
ResponsibilitiesOversees multiple projects, strategic planning, and department leadershipManages daily operations of clinical trials, supervises teams, and ensures compliance
Required CredentialsTypically requires a PhD, MD, or advanced degree, along with extensive experienceUsually requires a bachelor's or master's degree in life sciences, with relevant experience
Work EnvironmentSenior leadership in pharmaceutical or biotech companies, overseeing multiple teamsOperational setting within research sites or CROs, directly managing trial teams
Industry UsageCommonly found in large organizations with multiple projectsFound in both large and small organizations, focusing on trial execution

The Clinical Research Director focuses on strategic oversight and leadership of research programs, while the Clinical Research Manager handles day-to-day trial management. Both roles require relevant experience, but the director's role is more senior and strategic.

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 Director jobs in Riverside, RI look for?

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

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

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

Infographic showing various Clinical Research Director job openings in Riverside, RI as of June 2026, with employment types broken down into 3% As Needed, 89% Full Time, 7% Part Time, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $110,918 per year, or $53.3 per hour.

Assoc Director of Clinical Chemistry

Brownhealth

Providence, RI • On-site

Full-time

Posted 24 days ago


Key responsibilities

  • Provide technical and administrative assistance in the Clinical Chemistry Laboratory.

  • Participate in quality control and quality assurance programs related to clinical chemistry.

  • Collaborate in overseeing aspects of the point-of-care testing program and send-out department.


Brown University Health rating

6.7

Company rating: 6.7 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

534th of 898 rated healthcare providers


Job description

POSITION SUMMARY:

The role of Associate Director of Clinical Chemistry will provide technical and administrative assistance in the Clinical Chemistry Laboratory. In addition, the incumbent will provide quality control of all assays performed in the chemistry laboratory, provide activity reports, and ensure up-to-date knowledge of new technologies for the laboratory. The incumbent will participate in quality control and quality assurance programs as they relate to clinical chemistry. In addition, the associate director of chemistry will collaboratively oversee certain aspects of the point-of-care testing program and send-out department, as delegated by the system medical director of clinical laboratories. The Associate Director of Clinical Chemistry will also participate in the activities of the department including conferences with clinical departments in the hospital and at the Brown University School of Medicine.

The incumbent will be expected to develop and maintain an independent research program in the general area of clinical chemistry. The incumbent will also be expected to participate in the teaching of residents and fellows in the Department and in the teaching of Pathology and Laboratory Medicine courses and clerkships to medical students at Brown University and to provide instructional support to the medical technologist training program in the Department of Pathology.

The Pathologist should refer to letter of job offer regarding additional individual duties and responsibilities along with any faculty appointment and any applicable administrative function or title.

KEY ACCOUNTABILITIES:

Consistently applies the corporate values of respect, honesty and fairness and the constant pursuit of excellence in improving the health status of the people of the region through the provision of customer-friendly, geographically accessible and high-value services within the environment of a comprehensive, integrated academic health system. Is responsible for knowing and acting in accordance with the principles of the Brown University Health Corporate Compliance Program and Code of Conduct.

Participates in all quality control and quality assurance programs for clinical pathology.

Participates in activities of pathology and interfaces with various clinical departments at The Miriam and Rhode Island Hospitals and in the Brown Medical program.

Participates in Pathology conferences within the department and organizes, supports and assigns staff/residents to provide professional support/teaching in related interdepartmental conferences.

Teaching and Research:

The incumbents will also be expected to participate in the teaching of residents and fellows in the Department and in the teaching of Pathology and Laboratory Medicine courses, in supervising clerkships for medical students at Brown University and/or in providing instructional support to the medical technology training programs in the Department of Pathology.

Participates in teaching Pathology and Laboratory Medicine courses, clerkships offered to medical students at Brown University, graduate medical education programs (residents in pathology and other disciplines), and/or provides instructional support to the medical technologist training program and other similar programs of the Department of Pathology and Laboratory Medicine.

Establishes and continues independent research and development programs emphasizing, but not limited to, issues pertaining to anatomic pathology. Appropriate areas might be application of molecular and other probes to clinical diagnoses, use of information systems as clinical and research tools, application of morphometrics to clinical/research materials, or basic research and development in such areas as neoplasia, inflammatory processes, immunologic and degenerative/infectious conditions. It is expected that approximately 20% of the incumbent's time will be devoted to research related work.

PERFORMANCE STANDARDS:

  • Effective utilization of resources

  • Management of continuous quality improvement

  • High quality, high value patient-centered services

  • Resource productivity

  • Fiscal responsibility

  • Development and implementation of effective quality programs

  • Customer satisfaction

  • Performance improvements year-to-year

  • Positive feedback from peers, directs reports and staff

BASIC KNOWLEDGE:

  • Rhode Island MD licensure

  • Pathologist who is Board certified/board eligible in Clinical Laboratory Sciences (Clinical Pathology), or equivalent certification.

  • Eligible for Medical Staff membership at Rhode Island Hospital and The Miriam Hospital

  • Eligible for a faculty appointment at the Warren Alpert School of Medicine of Brown University.

  • Incumbents with a Ph.D. degree must be certified or eligible for certification by the American Association of Clinical Chemistry or the National Registry of Certified Chemists

  • 5-year experience requirement for the Associate Director level

EXPERIENCE:

Board certified in Clinical Pathology, with subspecialty certification in Clinical Chemistry, or equivalent experience and credentials.

Qualified to serve as a Clinical Provider in Rhode Island, with certification or other appropriate qualification for subspecialty area.

INDEPENDENT ACTION:

Incumbent functions independently within the department's policies and procedures. When clarification of policies and procedures is required, refers specific complex issues to the Director of the Section to whom direction has been delegated or escalates to the Medical Director of the clinical laboratories/ Chief of Pathology and Laboratory Medicine, whe indicated.

WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS:

Sits, stands, and walks intermittently throughout the day. Job requirements entail long periods of microscope use in order to perform work related responsibilities.

OTHER DUTIES AND RESPONSIBILITS AS ASSIGNED:

Additionalduties,responsibilitiesand authority may be assigned by the Department Chief from time to time in his/her sole discretion as deemed necessary to meet the operational needs of the Department.

Pay Range:

-

EEO Statement:

Brown University Health is committed to providing equal employment opportunities and maintaining a work environment free from all forms of unlawful discrimination and harassment.

Location:

Rhode Island Hospital - 593 Eddy Street Providence, Rhode Island 02903

Work Type:

M-F 8:00am-5:00pm

Work Shift:

Day

Daily Hours:

8 hours

Driving Required:

No

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