1

Clinical Research Project Manager Jobs in Rhode Island

Research Supv PD

Providence, RI · On-site

$35.90 - $59.23/hr

Participates with the principal investigator in the development, design and data management ... Provides for training and orientation to clinical research project(s). Coordinates work schedule ...

Participates with the principal investigator in the development, design and data management ... Provides for training and orientation to clinical research project(s). Coordinates work schedule ...

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 ...

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.

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.

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.

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.

next page

Showing results 1-20

Clinical Research Project Manager information

See Rhode Island salary details

$49K

$84.3K

$129.3K

How much do clinical research project manager jobs pay per year?

As of Aug 29, 2026, the average yearly pay for clinical research project manager in Rhode Island is $84,252.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $89,600.00 per year, depending on experience, location, and employer.

What does a clinical research project manager do?

A Clinical Research Project Manager oversees the planning, execution, and management of clinical research studies. They coordinate teams, ensure regulatory compliance, manage budgets and timelines, and act as a liaison between stakeholders such as sponsors, investigators, and regulatory agencies. Their primary goal is to ensure that clinical trials are conducted efficiently, ethically, and according to protocol. This role requires strong organizational, leadership, and communication skills, as well as a deep understanding of clinical research processes.

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

To thrive as a Clinical Research Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with tools such as CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications like PMP or ACRP-PM is highly valuable. Strong leadership, communication, and problem-solving skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial to ensure trials are conducted efficiently, ethically, and in line with regulatory standards.

What are some common challenges faced by clinical research project managers and how can they be addressed?

Clinical Research Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance, and coordinating communication between diverse stakeholders. Balancing the needs of sponsors, research teams, and regulatory bodies requires strong organizational and problem-solving skills. Staying proactive with risk management and fostering clear, consistent communication can help address these challenges effectively. Leveraging project management tools and regularly scheduled check-ins also supports smoother project execution and team collaboration.

What is the difference between Clinical Research Project Manager vs Clinical Research Coordinator?

AspectClinical Research Project ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in health sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, and liaises with sponsorsConducts daily clinical trial activities, interacts directly with participants and site staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch hospitals, clinics, academic institutions

The Clinical Research Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, ensuring protocol adherence and participant safety. Both roles are essential but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Research Project jobs in Rhode Island?

The most popular types of Clinical Research Project jobs in Rhode Island are:

What are popular job titles related to Clinical Research Project Manager jobs in Rhode Island?

For Clinical Research Project Manager jobs in Rhode Island, the most frequently searched job titles are:

What cities in Rhode Island are hiring for Clinical Research Project Manager jobs?

Cities in Rhode Island with the most Clinical Research Project Manager job openings:

Infographic showing various Clinical Research Project Manager job openings in Rhode Island as of August 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 90% In-person, and 10% Hybrid job distribution, with an average salary of $84,252 per year, or $40.5 per hour.

$35.90 - $59.23/hr

Full-time

Re-posted 27 days ago


Brown University Health rating

6.7

Company rating: 6.7 out of 10

Based on 95 frontline employees who took The Breakroom Quiz

532nd of 895 rated healthcare providers


Job description

SUMMARY: Under the general supervision of the Principal Investigator(s), and in accordance with established policies and procedures, supervises activities of subordinate professional and support staff assigned to one or more clinical research projects. Selects, orients, schedules, assigns work and evaluates performance of subordinate research staff. Ensures implementation of approved research program, adherence to research protocols, development and maintenance of study records. Assists investigator in interpretation of resultant data. May assist in preparation, writing and presentation of related research topics. Provides consultation within area of expertise to individuals, both internal to the department and hospital. Monitors budgets, including identification and reconciliation of variances. Brown University Health employees are expected to successfully role model the organization’s values of Compassion, Accountability, Respect and Excellence, as these values guide our everyday actions with patients, customers and one another. In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include: Instill Trust and Value Differences Patient and Community Focus and Collaborate In addition, our leaders will demonstrate an aptitude for: Ensure Accountability and Build Effective Teams Drive Vision and Purpose and Optimize Work Processes By applying core and leadership competencies, leaders help Brown University Health achieve its strategic goals. RESPONSIBILITIES: Participates with the principal investigator in the development, design and data management specific to one or more large clinical research studies. Participates in developing protocols, intervention plans and subject recruitment. Provides for the tabulation and analysis of data results for publication and reporting.Supervises non-MD/PhD research staff, including authoritatively recommending selection and as appropriate corrective action up to and including recommendation for termination. Participates in interview and selection of staff. Conducts annual evaluation of subordinate professional and support research staff. Provides for training and orientation to clinical research project(s). Coordinates work schedule, monitors adherence to procedures/protocols to ensure optimal patient participation rates, accurate data collection, etc.Assumes primary responsibility for the communication of Brown University Health policies and procedures for research and administrative functions within the assigned area. Provides assistance in the establishment of hypotheses and designs research protocols for same.Organizes and implements the protocol of the project, provides direct services as outlined by the grant criteria. Provides direction for the clinical research project. May function as needed in the role of senior clinical research assistant.Ensures accurate and complete collection of research data and development of associated database and reports. Analyzes resultant research data and participates in interpretation of same with investigator. May assist in the preparation and presentation of research papers.Participates with research investigators in development of the budget. Regularly monitors monthly budget reports, identifying and resolving variances, ensuring accuracy and conformance to budget. Within Brown University Health and department guidelines authorizes purchases related to research project. May order capital equipment as approved within budget.Contacts individuals both internal and external to the hospital to provide professional consultation within area of expertise and to exchange information.Functions as resource person during audits or on-site visits by the pharmaceutical companies and other related professional groups seeking information related to the research project.Reviews current literature for update approaches to research being conducted. May assign review of specific literature to research staff, requiring preparation and submission of summary analysis.Maintains quality assurance, safety, environmental and infection control in accordance with established hospital department policies and objectives. Coordinates and/or conducts annual training in these areas.May require outside travel to evaluate sites or for other grant-related reasons.Maintains and enhances professional expertise through educational opportunities and review of pertinent literature. MINIMUM QUALIFICATIONS: BASIC KNOWLEDGE:Masters Degree in relevant discipline is required.Excellent computer skills and familiarity with statistics.May require valid driver’s license where grant requires travel outside of hospital.EXPERIENCE:Five years progressively more responsible related clinical research experience, including demonstrated supervisory skills and effective interpersonal/communication skills.SUPERVISORY RESPONSIBILITY:Provides direct supervision for up to 20 full-time equivalent personnel assigned to the program.While most duties are performed in an office environment, incumbent is exposed to patient care environment.Any risk of exposure to contagious or noxious elements is minimized by adherence to safety procedures and protocols.

Pay Range:

$35.90-$59.23

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:

variable

Work Shift:

Variable

Daily Hours: 

Per Diem - As required

Driving Required:

No

What Brown University Health employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom