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Clinical Operations Manager Jobs in Westerly, RI

Clinical Research

Wakefield, RI ยท On-site

$16.25 - $20.30/hr

... operational resources physicians need to grow thriving practices for the future. As a Management ... The Clinical Researcher will develop, implement, and coordinate research and administrative ...

The Clinical Lead (CL) provide direction and guidance to multi-country clinical teams in assigned project(s), coordinate site management and monitoring activities, and provide operational leadership ...

It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic ... Uses Operational Excellence and Lab Management tools (ie training and capabilities matrices ...

It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic ... Uses Operational Excellence and Lab Management tools (ie training and capabilities matrices ...

Physical Therapist

Franklin, CT ยท On-site

$1.4K - $1.8K/wk

... daily clinical operations. Provide physical therapy services to Orthopedic Partners patients ... Align all work and resource management with the facility's mission, vision, philosophies and values ...

Showing results 21-40

Clinical Operations Manager information

See Westerly, RI salary details

$35.3K

$98.8K

$187.9K

How much do clinical operations manager jobs pay per year?

As of Aug 18, 2026, the average yearly pay for clinical operations manager in Westerly, RI is $98,758.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,000.00 and $114,300.00 per year, depending on experience, location, and employer.

What is a clinical operations manager?

Clinical Operations Managers are professionals responsible for overseeing the day-to-day administrative and operational functions of clinical trials or healthcare facilities. They ensure that clinical protocols are followed, resources are efficiently allocated, and regulatory compliance is maintained. These managers coordinate between healthcare staff, researchers, and external partners to facilitate smooth clinical operations and high-quality patient care. Their role is essential in ensuring that clinical services or trials are delivered effectively, safely, and on schedule.

What does a clinical operations manager do?

A clinical operations manager or director is a health care professional who oversees the operations of a medical facility. Their duties include meeting regularly with department heads, reading assessments of employee productivity, and managing administrative tasks, such as budgeting and billing. Qualifications for a clinical operations manager include experience in medical administration, management skills, and organizational skills. An advanced degree in public health or health administration can significantly improve your job opportunities.

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

To thrive as a Clinical Operations Manager, you need expertise in clinical trial management, regulatory compliance, and healthcare operations, usually supported by a degree in a health-related field and relevant experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as ACRP or SOCRA are commonly required. Strong leadership, problem-solving abilities, and effective communication are essential soft skills for this role. These skills ensure efficient trial execution, regulatory adherence, and successful coordination across teams and stakeholders.

What are the main challenges clinical operations managers face when overseeing multiple clinical trials simultaneously?

Clinical Operations Managers often juggle several clinical trials at once, which can present challenges such as maintaining consistent quality across studies, ensuring timely patient recruitment, and managing diverse teams. They must coordinate with cross-functional departments, address regulatory compliance, and troubleshoot unforeseen issues, all while staying on schedule and within budget. Effective organizational skills, proactive communication, and adaptability are essential for overcoming these challenges and ensuring successful trial outcomes.

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

AspectClinical Operations ManagerClinical Research Coordinator
CredentialsBachelor's degree in health sciences, management experienceBachelor's degree in health or life sciences, research training
Work EnvironmentOversees multiple clinical trials, manages teamsAssists with daily trial activities, data collection
Employer & IndustryPharmaceutical companies, CROs, hospitalsResearch institutions, hospitals, clinical sites

The Clinical Operations Manager focuses on overseeing entire clinical trial operations, managing teams, and ensuring compliance. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, such as patient recruitment and data collection. Both roles require related credentials and work within the clinical research industry, but their responsibilities and scope differ significantly.

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What are the most commonly searched types of Clinical Operations jobs in Westerly, RI?

The most popular types of Clinical Operations jobs in Westerly, RI are:

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The top searched job categories for Clinical Operations Manager jobs in Westerly, RI are:

What cities near Westerly, RI are hiring for Clinical Operations Manager jobs?

Cities near Westerly, RI with the most Clinical Operations Manager job openings:

Infographic showing various Clinical Operations Manager job openings in Westerly, RI as of August 2026, with employment types broken down into 82% Full Time, 15% Part Time, 1% Temporary, and 2% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $98,758 per year, or $47.5 per hour.

Clinical Research

Spire Orthopedic Partners

Wakefield, RI โ€ข On-site

$16.25 - $20.30/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday


Job description

Who we are:ย 

Spire Orthopedic Partners is a growing national partnership of orthopedic practices that provides the support, capital and operational resources physicians need to grow thriving practices for the future. As a Management Services Organization (MSO), Spire provides the infrastructure for administrative operations that allows practices to operate at their highest level, so doctors can focus their efforts on what matters most โ€“ patient care. Headquartered in Stamford, the Spire network spans the Northeast with more than 165 physicians, 1,800 employees, 285 other clinical providers and 40 locations in New York, Connecticut, Rhode Island and Massachusetts.

Ortho Rhode Island is a world-class group of talented providers and professionals, all working together to offer value and quality in everything we do. Each Ortho Rhode Island team member is dedicated to thinking like a patient, and to offering the best experience in our industry, driven by our core values: delivering on our word, respecting each other, innovating in orthopedics, valuing every individual, and engaging our community.ย 

What youโ€™ll do:ย 

The Vision of the Clinical Researcher is the essential link in providing a team-based approach to patient care and an exceptional patient experience. The Clinical Researcher will emphasize highly personalized care and help patients surpass barriers to healthcare by improving the patient/provider relationship.

The Clinical Researcher is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator. The Clinical Researcher will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The Clinical Researcher will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols.

Responsibilities/Duties:

  • Collect and organize data and compile for progress reports
  • Coordinate with research assistants/ student employees, provide guidance and assistance as needed
  • Assist and coordinate with Research Manager to ensure clinical research and activities are performed in accordance with approved IRB
  • Discuss study protocols with patients and verify the informed consent documentation
  • Provide patient with written communication of their participation (i.e. copy of the signed informed consent)
  • Adhere to Good Clinical Practices and the study protocols
  • Ensure scientific integrity and accuracy of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
  • Prepare findings for publication and assist in laboratory analysis, quality control, or data management
  • Write and contribute to publications
  • Ensure that non-serious and serious adverse events are properly documented and reported
  • Liaison to partnering hospitals other research sites for new and existing patients
  • Prepare and submit initial review of new studies to IRB
  • Assist with overflow Medical Assistant duties
  • Compliance with HIPAA and OSHA regulations
  • Other duties may be assigned as necessary

Who you are:

Qualifications:

  • Bachelor's degree in Human Health Care or related field required.
  • Any combination of education, training, and experience that demonstrates the ability to perform the duties of the position.
  • Experience with Electronic Medical Records
  • Excellent computer skills
  • EMR Systems
  • Practice Management System
  • Microsoft Suite (including: Outlook, Word, Excel, Calendar)
  • Phone softwareย 
  • Navigating Insurance Authorization websites
  • Knowledge of estimated co-payment and co-insurance
  • Specialties such as: Spine, Joints/Trauma, Sports Medicine, Foot/Ankle, and Hand/Microsurgery
  • General understanding of processing legal forms
  • Ability to collaborate with supervisory teams and administrators on projects or assigned tasks

What we offer:ย 

  • Excellent growth and advancement opportunitiesย 
  • Dynamic environmentย 
  • Access to a diverse network of practitionersย 
  • Broad infrastructure of tools and programs to enhance the employee experience ย  ย 
  • Competitive Compensationย 
  • Generous PTOย ย 
  • Benefits package: health, dental, vision, 401(k), etc.ย 

We are an equal-opportunity employer. Qualified Applicants are considered for positions and are evaluated without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex, or gender (including pregnancy, childbirth, and related medical conditions), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, protected medical condition as defined by applicable state or local law, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances (referred to as โ€œprotected characteristicsโ€).ย ย 
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