Top 7 Clinical research manager Jobs in Worcester Ma

Clinical Study Coordinator/Manager
Propedix, Inc. —Milford, MA
- $25 - $30 an hour
- Part-time
- Hybrid work
- 5 years
- Mid-level
- Bachelor's degree
Quick Apply
Senior Manager, Global Clinical Affairs Data (Hybrid - Acton, MA)
Insulet Corporation —Acton, MA
- $147,000 - $220,500 a year
- Full-time
- Hybrid work
- 6 years
- System design
- HIPAA
- Health insurance
- Dental insurance
12d
Manager, Medical Information
Sequel Med Tech —Marlborough, MA
- $75,000 - $140,000 a year
- Extended hours
- Hybrid work
- Nursing
- Medicine
- 5 years
- Health savings account
- Paid holidays
Senior Manager, Project Manager - Biologics
Bristol-Myers Squibb —Devens, MA
- $135,200 - $163,832 a year
- Email
- Hybrid work
- Microsoft Excel
- Microsoft Access
- Bachelor of Science
- Paid holidays
- Disability insurance
Product Marketing Manager - Medical
IPG Photonics —Marlborough, MA
- $99,131 - $131,348 a year
- Marketing
- 5 years
- Writing skills
- Health savings account
- AD&D insurance
Quick Apply
Project Lead
Hamilton Storage Technologies —Franklin, MA
- $115,000 - $135,000 a year
- Full-time
- 5 years
- Bachelor's degree
- Experience equivalent to degree accepted
- Disability insurance
- Health insurance
Project Lead | Project Management Group
Hamilton Storage Technologies —Franklin, MA
- $80,000 - $100,000 a year
- Full-time
- Construction site
- 5 years
- Engineering
- Disability insurance
- Health insurance

More jobs to discover

Find similar jobs that you might be interested in.

Senior Manager, Global Clinical Affairs Data (Hybrid - Acton, MA)
Insulet Corporation —Acton, MA
The position also drives process improvements, develops study metrics and tracking tools, supports investigator training, and serves as a subject matter expert…
$147,000 - $220,500 a year
12d

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Project Manager - Institute for Genomic Medicine
Nationwide Children's Hospital —Columbus, OH
Bachelor's Degree in relevant field, or equivalent experience, required. Responsibilities include communications, reporting, data analysis, financial and grant…
IT Project Manager
The Ohio State University Wexner Medical Center —Columbus, OH
Working closely with clinical, research, academic, and administrative stakeholders, the Project Manager coordinates cross-functional teams, manages project…
5d

Show more jobs in cities nearby

I want to receive the latest job alert for clinical research manager in worcester ma

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical research manager jobs near worcester ma

Project Manager jobs in Franklin, MA

Project Manager jobs in Tallahassee, FL

Project Lead jobs in Downers Grove, IL

Project Lead jobs in Maryland

Project Coordinator jobs in Phoenix, AZ

Project Lead jobs in Greenville, SC

Project Lead jobs in Milwaukee, WI

Senior Clinical Data Analyst jobs in Charlotte, NC

Discovery Senior Living jobs in Florida

Senior Clinical Data Analyst jobs in Madison, NJ

Senior Clinical Data Analyst jobs in California

Brookdale Senior Living jobs in Seattle, WA

Brookdale Senior Living jobs in Madison, WI

Senior Clinical Data Analyst jobs in Chicago, IL

Remote Project Manager jobs in Fort Worth, TX

Office Manager jobs in Miami, FL

Entry Level Construction Project Manager jobs in Tampa, FL

Project Manager jobs in New Orleans, LA

Project Manager jobs in Asheville, NC

Project Manager jobs in Augusta, GA

Clinical Study Coordinator/Manager

Propedix, Inc.
Milford, MA

Quick Apply

Job Details

Part-time
$25 - $30 an hour

Qualifications

Filing
Bachelor's degree
Clinical quality assurance standards
FDA regulations
Research compliance quality assurance records management

Full Job Description

Job Description – Clinical Study Manager/Coordinator

About the Company: Propedix is a biopharma and consumer health company dedicated to advancing innovative treatments in healthcare. Our flagship product, featuring our breakthrough anti-fungal and drying agent technology, launched in Q3 2025, and we have a pipeline of advanced OTC and Rx treatments in dermatology and health. The Company has a pipeline of new skin infection treatment productions planned for launch throughout 2026. All based on the company DryStiK SM Tech Platform. Driven by strong research and development, we’re delivering the next generation of health solutions.

Position: Clinical Study Manager or Coordinator

Position Overview:

The Clinical Study Manager or Coordinator (CSM or CSC) will support the planning, initiation, execution, and closeout of clinical studies across Propedix’s dermatology pipeline. This role will work closely with internal leadership, investigators, CRO partners, and clinical sites to ensure studies are conducted in compliance with regulatory requirements, Good Clinical Practice (GCP), and study protocols.

This is a full-time (30 hours/week), hybrid (on-site and remote), 1099 contractor role ideal for candidates with strong clinical research experience who are comfortable working in a fast-paced startup environment.

Key Responsibilities:

Study Start-Up & Regulatory

Support and contribute to protocol development, study materials, and operational plans

Coordinate IRB submissions, approvals, amendments, and site activation activities

Prepare and maintain essential regulatory documents and investigator site files

Support site selection, feasibility assessments, site readiness, and site initiation activities

Clinical Trial Operations

Serve as a primary point of contact for external clinical sites and investigators

Track and report key study performance metrics, including enrollment targets, retention rates, and milestone progress, and implement strategies to address gaps or delays

Lead participant recruitment efforts, including screening for eligibility, explaining the study, and facilitating enrollment

Obtain and document informed consent from study participants in accordance with GCP, IRB requirements, and the study protocol

Manage patient visits, including scheduling, data collection, and source documentation

Ensure protocol adherence, track protocol deviations, and troubleshoot operational challenges

Support and conduct site initiation training on protocol procedures, workflows, and GCP standards

Data Collection & Quality Management

Oversee accurate and timely completion of case report forms (CRFs), including paper-based systems

Demonstrate familiarity with common clinical trial systems and tools, including electronic data capture (EDC) platforms, clinical trial management systems (CTMS), and hybrid workflows integrating paper-based CRFs with electronic systems

Perform data entry oversight, validation, and quality checks to ensure data integrity

Coordinate secure transfer of de-identified datasets to internal teams or external partners

Maintain Trial Master File (TMF) and ensure audit readiness

Support monitoring activities (remote and onsite) and implement corrective actions as needed

Safety & Compliance

Track and report adverse events (AEs), serious adverse events (SAEs), and protocol deviations per regulatory requirements

Ensure studies are conducted in accordance with GCP, FDA regulations, and applicable guidelines

Support preparation for audits, inspections, and site qualification visits

Cross-Functional Collaboration

Work closely with internal clinical, regulatory, and product development teams

Coordinate with external vendors

Facilitate communication between sponsor, investigators, CRO partners, and study sites

Participate in study meetings and provide regular status updates

Relay clinical progress, key findings, and operational challenges to internal stakeholders

Location: Candidate must live in the greater Boston MSA and within 30 minute drive to In-person in Milford and Framingham, Massachusetts. Regular on-site presence is required to support clinical operations, with occasional travel as needed for site visits or study-related activities.

Experience/ Necessary Skills

Education: Bachelor’s degree in STEM discipline

Experience:

Required:

2+ years (CSC) and 5+ years (CSM) of experience coordinating clinical trials, including site management and regulatory processes

Familiarity with GCP, FDA regulations, and IRB procedures

Experience with CRFs (paper or electronic) and clinical data management

Strong organizational and communication skills

Ability to work independently in a fast-paced environment

Preferred:

Experience in dermatology or topical drug studies

Experience with sponsor-side coordination or multi-site studies

Familiarity with Trial Master Files (TMF) and audit readiness processes

Exposure to CRO collaboration and vendor management

Hours: Approximately 30 hours per week. Candidates are required to attend a company-wide meeting on Tuesday evenings. This role follows a hybrid schedule, consisting of three in-person days and one remote day per week. A flexible schedule is required, including availability for occasional evening and weekend work, with the ability to complete certain responsibilities remotely as needed.

Compensation: $35 to $40/hr for CSM and $25 to 30/hr for CSC. This is an independent contractor 1099 position.

Support and Supervisor: The position reports to the Chief Medical Officer who will be their administrative supervisor and will also work closely with clinical vendors and the formulation team.

Application: Interested parties should send their resume and a brief cover note to [email protected].

Quick Apply

Refine Your Search

clinical research manager jobs in worcester ma

Clinical Study Coordinator/Manager

Senior Manager, Global Clinical Affairs Data (Hybrid - Acton, MA)

Manager, Medical Information

Senior Manager, Project Manager - Biologics

Product Marketing Manager - Medical

Project Lead

Project Lead | Project Management Group

More jobs to discover

Explore jobs in cities nearby

I want to receive the latest job alert for clinical research manager in worcester ma

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected