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Associate Clinical Project Manager Jobs in Rhode Island

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 ...

Manage most aspects of these clinical projects to include: - Serve as the main contact for research participants throughout all aspects of the research study. Identify patients meeting criteria for ...

Project Assistant

Providence, RI · On-site

$24.48 - $34.38/hr

PAs also assist project managers in managing sites through the Rhode Island Department of ... Associate or bachelor's degree in related field preferred. * Experience with ArcGIS Pro preferred.

PAs also assist project managers in managing sites through the Rhode Island Department of ... Associate or bachelor's degree in related field preferred. * Experience with ArcGIS Pro preferred.

SURVEY MANAGER

Lincoln, RI · On-site

$62.50 - $68.30/hr

The Survey Manager oversees survey projects from initiation to completion. They will supervise ... Associate's or Bachelor's degree * Previous supervisory experience COMPUTER SKILLS * Proficient in ...

Clinical Manager

Warwick, RI · On-site

$100K - $118K/yr

Associate or bachelor's degree in nursing. * Current RN license, specific to the state(s) you are ... One year of clinical RN experience in home health or hospice. * One year of RN management ...

Showing results 41-60

Associate Clinical Project Manager information

See Rhode Island salary details

$16

$37

$58

How much do associate clinical project manager jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for associate clinical project manager in Rhode Island is $37.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.18 and $44.04 per hour, depending on experience, location, and employer.

What is an associate clinical project manager?

An Associate Clinical Project Manager (ACPM) is an entry- to mid-level professional who assists in planning, coordinating, and overseeing clinical trials and research projects within pharmaceutical, biotech, or clinical research organizations. They work closely with project managers and cross-functional teams to ensure studies are conducted according to protocol, regulatory requirements, and timelines. ACPMs may handle tasks such as tracking project progress, supporting site management, preparing documentation, and communicating with stakeholders. Their role helps ensure the smooth execution and delivery of clinical research projects.

What are the key skills and qualifications needed to thrive as an associate clinical project manager?

To thrive as an Associate Clinical Project Manager, you need a solid understanding of clinical research processes, project management principles, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often required. Exceptional organizational skills, attention to detail, and strong communication abilities help you coordinate teams and timelines effectively. These competencies are crucial for ensuring clinical trials run smoothly, meet regulatory standards, and deliver reliable results on schedule.

What are the common challenges faced by an associate clinical project manager and how can they be addressed?

Associate Clinical Project Managers often encounter challenges such as balancing multiple study timelines, coordinating cross-functional teams, and ensuring regulatory compliance. Managing communication between sponsors, vendors, and internal teams can also be complex. To address these challenges, it's important to prioritize tasks, maintain clear documentation, and foster strong relationships with stakeholders. Leveraging project management tools and regularly reviewing project milestones can help ensure studies stay on track and issues are promptly resolved.

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

AspectAssociate Clinical Project ManagerClinical Project Coordinator
CredentialsBachelor's degree, often some project management or clinical research experienceBachelor's degree, entry-level in clinical research
Work EnvironmentSupports project managers, involved in planning and oversightAssists with daily tasks, data collection, and site communication
Employer & Industry UsagePharmaceutical, biotech, clinical research organizationsClinical research sites, CROs, pharma companies

The Associate Clinical Project Manager typically has more responsibility in project planning and oversight compared to the Clinical Project Coordinator, who mainly supports data collection and site coordination. Both roles are essential in clinical research teams, with the associate role often serving as a stepping stone to more senior project management positions.

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

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

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

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

What job categories do people searching Associate Clinical Project Manager jobs in Rhode Island look for?

The top searched job categories for Associate Clinical Project Manager jobs in Rhode Island are:

Infographic showing various Associate Clinical Project Manager job openings in Rhode Island as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $78,929 per year, or $37.9 per hour.

$55K - $91K/mo

Full-time

Posted 15 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

534th of 898 rated healthcare providers


Job description

SUMMARY: Under general supervision of the Research Program Manager and the Director of the Center for Behavioral and Preventive Medicine (CBPM), and in accordance with established policies and procedures, the Research Project Director is responsible for the operation of projects, including recruitment, implementation programs, processes, and outcome evaluation of CBPM projects and core related projects within the COBRE for Stress, Trauma, and Resilience. The Research Project Director will liaison with other internal and external departments as required. 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 RESPONSIBILITIES: In collaboration with Principal Investigators and the Research Program Manager, assesses needs and identifies mission-critical tasks to meet overall goals of the project. Collaborates in the development and execution of project and core goals, establishment of datelines, and the development of long and short-range strategic implementation plans. Collaborates with research project Principal Investigators and cores to ensure grant goals including timelines and deadlines are met. Works with the Research Program Manager to provide administrative and logistical management of daily operations. Includes assessing grant activity to assure compliance with grant requirements, assures all required reporting is completed on time, monitoring of monthly expense reports for accuracy and conformance to budget and addresses variances as required to meet the budget. Coordination of sub-contracts with affiliated hospitals and universities may be required. Assists the Principal Investigators of Projects with protocols, intervention plans, and recruitment, IRB submissions and assists with other laboratory needs, as required. Organization and assistance with the implementation of clinical protocols of the project and provision of direct services may be required. Assists the Principal Investigators of Cores with administrative support and operational and strategic plans. Oversees core deliverables and is responsible for tracking and reporting core usage. Travels, to evaluate sites, or for other grant-related reasons, as required. Provides supervision and oversight to staff. Hires, trains, schedules, conducts periodic performance evaluations, provides guidance and counsels to assistants and other designated staff to endure high quality recruitment and related data gathering. Maintains quality assurance, safety, environmental, and infection control in accordance with established hospital department policies and objectives. MINIMUM QUALIFICATIONS: BASIC KNOWLEDGE: Equivalent to Master’s Degree in relevant discipline. Knowledge of research grants administration and current reporting requirements. EXPERIENCE: Two to three years relevant experience, depending on size and complexity of grants, including supervisory, clinical and/or diagnostic interviewing. Experience with multi-year, multi-site studies and at-risk populations and community-based programs is essential. Knowledge of SPSS, REDCap, and Excel is preferred. Supervisory and administrative experience desirable. WORK ENVIRONMENT AND PHYSICAL REQUIREMENTS: 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. INDEPENDENT ACTION: Incumbent functions independently within a broad scope of department policies and practices; generally, refers specific problems to supervisor only where clarification of department policies and procedures may be required. SUPERVISORY RESPONSIBILITY: Provides direct supervision for up to 10 full-time equivalent personnel assigned to the project.

Pay Range:

$55,744.00-$91,956.80

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:

The Miriam Hospital - 164 Summit Ave Providence, Rhode Island 02906

Work Type:

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

Work Shift:

Day

Daily Hours: 

8 hours

Driving Required:

No

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