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Clinical Jobs in Smithfield, RI

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Director Medical Affairs - Clinical Microbiology Waters Corporation

Boston, MA

The Director is expected to bring deep diagnostic and laboratory expertise, strong business acumen, and a collaborative leadership style to advance medical credibility, innovation, and patient impact across Waters Advanced Diagnostics. This individual translates unmet customer and patient needs, evolving clinical practice, and real-world evidence into actionable medical strategies that strengthen product differentiation, support lifecycle decisions, and enable successful development and adoption of innovative diagnostic solutions.

24 days ago

Clinical Faculty, Doctoral Program in Clinical Psychology (Psy.D.) Trustees of Bryant University

Smithfield, RI

The Psychology department is a flagship department in the growing College of Health and Behavioral Sciences at Bryant University, which currently offers undergraduate majors in Psychology, Biology, Health Sciences, and Exercise and Movement Science, as well as graduate programs in Physician Assistant Studies and Healthcare Informatics and AI. Opportunities for interdisciplinary collaboration are encouraged with the Master of Science in Physician Assistant Studies, the Master of Science in Healthcare Informatics and AI, along with additional programs in the College of Health and Behavioral Sciences as well as the College of Humanities and Social Sciences and the College of Business.

11 days ago

Clinical Research Associate Alira Health

Framingham, Massachusetts

CRAs work closely with the In-house CRAs, Lead CRAs, Director of Clinical Monitoring and Project Managers to ensure sites’ protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues. Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status.

30+ days ago

RN, Clinical Trial Manager UnitedHealth Group Inc

Worcester, MA

$60,200–$107,400 / year

Performs study-related procedures including, but not limited to, patient recruitment, informed consent, physical assessment, medical history, vital signs, administration of study medication, preparation and handling of laboratory specimens, identification of adverse events, and collection of all required data. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes - an enterprise priority reflected in our mission.

15 days ago

Product Manager - Veeva Clinical Operations Veeva Systems

Boston, MA

$75,000–$165,000 / year

Unlike a traditional corporation, whose only legal duty is to maximize shareholder value, PBCs consider their public benefit purpose and the interests of those materially affected by the corporation's conduct-including customers, employees, and the community-in addition to shareholders' interests. Working closely with cross-functional teams, you will help execute the product vision to unify clinical systems, streamline trial execution, and speed the delivery of new therapies to patients.

30+ days ago

Clinical Research Project Manager Mass General Brigham

Massachusetts

Other responsibilities include: assuming the regulatory lead for IRB protocol submissions, modifications, continuing reviews, reportable new information, and consent revisions; maintaining the study regulatory binder under single-IRB oversight at MGB, and maintaining compliance with Federal, State and sponsor (e.g., NIMH) guidelines, audits, and sponsor progress reports. Specifically, this position entails managing multiple clinical studies (e.g., including a randomized controlled trial), with day-to-day supervision and training of research coordinators and other staff, often involving multiple sites or stake-holders.

8 days ago

Clinical Pharmacist Specialist, Ambulatory Endocrinology RIH Rhode Island Hospital

Rhode Island

Within 6 months of start date, for positions that perform immunizations or medication administrations in accordance with Rhode Island Board of Pharmacy Rules and Regulations or the Commonwealth of Massachusetts, must possess and maintain an American Council for Pharmacy Education (ACPE) approved Immunization Certification and American Heart Association Basic Life Support (BLS) Certification. Conducts pharmacy practice research, clinical research, and data-related research in alignment with Brown University Health’s mission, goals, and priorities; authors original research-based abstracts, scientific, and scholarly papers and submits for publication and/or presentation in accordance with departmental policies and procedures.

30+ days ago

Medical Writer Clinical Development eTeam Inc.

Marlborough, MA

Remote

Quick Apply

Collaborate with cross-functional teams, including Clinical Development, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, and Medical Affairs, to gather, interpret, and integrate scientific and clinical information into clear, accurate, and submission-ready documents. This role works closely with cross-functional stakeholders to ensure documents are scientifically accurate, strategically aligned, and delivered according to established timelines and medical writing plans.

30+ days ago

Clinical Supervisor, LPN, Otolaryngology Clinic, 40 hours, Days UMass Memorial Health Care Inc

Worcester, MA

$62,004.80–$111,633.60 / year

Performs and coordinates a broad range of related functions to include direct patient care, telephone encounters, coordination of clinical support staff work assignments, staff scheduling and quality assurance initiatives. Provides daily assurance that all areas are properly staffed with clinical support staff (Patient Care Associates, Medical Assistants and / or Licensed Practical Nurses) that are trained for a particular area.

22 days ago

Regulatory Coordinator II - Clinical Trial Office Dana-Farber Cancer Institute Inc

Brookline, MA

Remote

$61,110–$67,900 / year

This position will work collaboratively with a variety of personnel at all levels, including faculty and study team members of DF/HCC and external institutions, cooperative groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations. Prepares and submits regulatory documentation that may include IND/IDE applications, FDA annual reports, Serious Adverse Event reports, to the appropriate regulatory agencies including the Food and Drug Administration (FDA), Office of Biotechnology Activities (OBA), etc.

30+ days ago

RN, Clinical Trial Manager Optum

Oakham, MA

$60,200–$107,400 / year

Today

Senior Manager, Clinical Nurse Educator – Sickle Cell Disease - Remote Agios Pharmaceuticals

Boston, MA

Remote

$127,219–$190,828 / year

Building on the company’s leadership in the field of cellular metabolism, Agios is advancing a robust clinical pipeline of investigational medicines with active and planned programs in alpha- and beta-thalassemia, sickle cell disease, pediatric PK deficiency and MDS-associated anemia. Our teams cultivate strong bonds with patient communities, healthcare professionals, partners and colleagues, which helps us discover, develop and deliver therapies for genetically defined diseases – and make a bigger difference in their lives.

24 days ago

Clinical Reviewer, Inpatient RN # 26-26518 US Tech Solutions, Inc.

Canton, MA

Quick Apply

Job Description: The Clinical Reviewer, Inpatient RN, is a licensed professional that is expected to function independently in her / his role and is responsible for managing a clinically complex caseload of members across one or more types of inpatient settings; acute, subacute, acute rehabilitation, LTAC, and others. The Clinical Reviewer, Inpatient RN provides timely, clinically appropriate and cost-effective utilization management and discharge planning activities for members receiving services at her / his assigned facilities and may be required to float to provide coverage at unassigned facilities.

1 day ago

Clinical Therapist VitalCore Health Strategies

Bridgewater, MA

$75,000–$110,000 / year

Some of the core tasks completed by Clinical Therapists include: In collaboration with the patient, develop monitor and, when clinically indicated modify individualized treatment plans to reflect therapeutic needs/goals. Prior experience working in the field of sexual abuse treatment and prevention is not required; all necessary training is provided following official hire.

5 days ago

Regional Clinical Therapist - SOT VitalCore Health Strategies

Bridgewater, MA

$75,000–$110,000 / year

Some of the core tasks completed by Clinical Therapists include: In collaboration with the patient, develop monitor and, when clinically indicated modify individualized treatment plans to reflect therapeutic needs/goals. These positions are based approximately three days/week onsite at Massachusetts Treatment Center and two days/week onsite at our other sites around Massachusetts.

5 days ago

Travel Licensed Clinical Social Worker (LCSW) in Canton, MA TalentBurst Inc.

Canton, MA

AND A current and valid licensure as a Licensed Social Work Associate, Licensed Social Worker, Licensed Certified Social Worker, or Licensed Independent Clinical Social Worker issued by the Massachusetts Board of Registration. Supports patient discharge activities, beginning on the day of admission, through caregiver education on the transition process, identification of patient discharge options, and coordination with community providers to ensure continuity of care.

8 days ago

Clinical Director - SOTP VitalCore Health Strategies

Bridgewater, MA

$165,000–$175,000 / year

The Clinical Director assists the Director of Sex Offense-Specific Program Services in monitoring all aspects of sex offense specific treatment (SOT) services at the Massachusetts Treatment Center (MTC). This position coordinates effective administration of SOT services as further described below and provides administrative guidance and support to site SOT staff, reporting to the Director of Sex Offense Specific Program Services.

5 days ago

PHLEBOTOMY MANAGER, INPATIENT Confidential

Boston, MA

$83,000–$120,000 / year
Full time
Quick Apply

Takes full fiscal responsibility for section oversights, including but not limited to: preparing and managing an operating budget, managing staffing expenses and overtime (OT), capital budget, analyzing billing codes, preparing return on investment business analysis, fully supporting the revenue integrity of the Laboratory including accurate charges, billing and collections. Management oversight and leadership of multiple sub-specialty sections of the Laboratory (including but not limited to one of the following: Blood Bank and Transfusion Services, Central Receiving Area, Chemistry, Hematology, Phlebotomy, POC or Rapid Response Laboratory).

8 days ago

Clinical Research Program Manager/Senior Clinical Research Program Manager Brigham and Women's Hospital

Boston, MA

$63,252.80–$102,596 / year

Recent work involving these clinical research programs has used multi-omic profiling to identify microbial features associated with response to biologic therapy, single-cell approaches to define immune dysregulation in Crohn's disease, and single-cell and spatial transcriptomics to identify cellular networks associated with intestinal fibrosis. The successful candidate will provide strategic and operational leadership across multiple clinical studies, supervise clinical research staff, and work closely with physicians, scientists, computational researchers, and institutional research teams to ensure that complex studies are executed rigorously and efficiently.

30+ days ago

Senior Clinical Research Associate/Clinical Research Associate II - US Any Region - FSP Parexel

Massachusetts

Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks. Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File (TMF) documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics.

4 days ago

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Clinical Jobs in Smithfield, RI

Director Medical Affairs - Clinical Microbiology Waters Corporation

Clinical Faculty, Doctoral Program in Clinical Psychology (Psy.D.) Trustees of Bryant University

Clinical Research Associate Alira Health

RN, Clinical Trial Manager UnitedHealth Group Inc

Product Manager - Veeva Clinical Operations Veeva Systems

Clinical Research Project Manager Mass General Brigham

Clinical Pharmacist Specialist, Ambulatory Endocrinology RIH Rhode Island Hospital

Medical Writer Clinical Development eTeam Inc.

Clinical Supervisor, LPN, Otolaryngology Clinic, 40 hours, Days UMass Memorial Health Care Inc

Regulatory Coordinator II - Clinical Trial Office Dana-Farber Cancer Institute Inc

RN, Clinical Trial Manager Optum

Senior Manager, Clinical Nurse Educator – Sickle Cell Disease - Remote Agios Pharmaceuticals

Clinical Reviewer, Inpatient RN # 26-26518 US Tech Solutions, Inc.

Clinical Therapist VitalCore Health Strategies

Regional Clinical Therapist - SOT VitalCore Health Strategies

Travel Licensed Clinical Social Worker (LCSW) in Canton, MA TalentBurst Inc.

Clinical Director - SOTP VitalCore Health Strategies

PHLEBOTOMY MANAGER, INPATIENT Confidential

Clinical Research Program Manager/Senior Clinical Research Program Manager Brigham and Women's Hospital

Senior Clinical Research Associate/Clinical Research Associate II - US Any Region - FSP Parexel

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