Top 99 Clinical research coordinator Jobs in Milford, Ma

Clinical Research Associate (CRA) – Temporary 6 Month Contract
Lighthouse Lab Services —Waltham, MA
- $45 an hour
- Temporary
- Nursing
- Medicine
- English
- Flexible schedule
Quick Apply
4d
Clinical Research Coordinator, Per Diem, Framingham Heart Study
Boston University —Framingham, MA
- Per diem
- Entry level
1d
Clinical Research Coordinator II
University of Massachusetts Medical School —Worcester, MA
- $23.08 - $27.88 an hour
- HIPAA
- Mid-level
- Bachelor's degree
9d
Clinical Research Assistant
University of Massachusetts Medical School —Worcester, MA
- $36,000 - $40,000 a year
- Full-time
- Microsoft Outlook
- Computer literacy
- Bachelor's degree
Clinical Research Asst II
Care New England Health System —Providence, RI
- Weekends as needed
- Inventory management
- Computer literacy
- Office
Clinical Research Coordinator II - Attleboro
Dana-Farber Cancer Institute —Attleboro, MA
- $56,000 - $62,700 a year
- Full-time
- Computer literacy
- Mid-level
- Bachelor's degree
Clinical Research Coordinator I
The Brigham and Women's Hospital, Inc. —Boston, MA
- $21.00 - $29.01 an hour
- Full-time
- Computer literacy
- Bachelor's degree
- Quality control
- Opportunities for advancement
Quick Apply
2d
Clinical Research Coordinator - Open Rank
University of Massachusetts Medical School —Worcester, MA
- $40,000 - $80,000 a year
- Full-time
- Hospital
- HIPAA
- Mid-level
Clinical Research Coord I
University of Massachusetts Medical School —Worcester, MA
- $19.23 - $23.08 an hour
- Part-time
- HIPAA
- Office
- Bachelor's degree
11d
Clinical Research Coordinator
The General Hospital Corporation —Waltham, MA
- $21.00 - $29.01 an hour
- Full-time
- Computer literacy
- Bachelor of Science
- No experience needed
- Opportunities for advancement
Quick Apply
10d
Clinical Research Associate
Alira Health —Framingham, MA
- Full-time
- Bachelor of Science
- English
- Mid-level
Clinical Research Coordinator III
University of Massachusetts Medical School —Worcester, MA
- $58,000 - $70,000 a year
- Full-time
- Mid-level
- 3 years
- Analysis skills
Administrative Coordinator - Large Animal Clinical Sciences
Tufts University —Grafton, MA
- $27.85 - $38.50 an hour
- 5 years
- Office
- Databases
9d
Clinical Research Coordinator - Cancer Genetics
Dana-Farber Cancer Institute —Boston, MA
- $48,100 - $54,400 a year
- Full-time
- Bachelor's degree
- Epic
- Public Health
Clinical Research Coordinator I - Urology
The Brigham and Women's Hospital, Inc. —Boston, MA
- $21.00 - $29.01 an hour
- Full-time
- Hybrid work
- Bachelor's degree
- Human resources
- Mentoring
- Opportunities for advancement
Quick Apply
Clinical Research Coordinator II - Foxborough
Dana-Farber Cancer Institute —Foxborough, MA
- $56,000 - $62,700 a year
- Full-time
- Mid-level
- Databases
- Bachelor's degree
Clinical Research Associate - Contract
Lumicell —Waltham, MA
- Contract
- Remote
- Nursing
- Mid-level
- Bachelor's degree
Quick Apply
Clinical Research Assistant I (MFM)
Care New England Health System —Providence, RI
- Weekends as needed
- Nursing
- Hospital
- Master's degree
Clinical Trials Research Coordinator
Brown University Health —Providence, RI
- $64,480.00 - $106,412.80 a year
- 8 hour shift
- Nursing
- Vital signs
- Hospital
Senior Clinical Research Coordinator - Milford
Dana-Farber Cancer Institute —Milford, MA
- $73,600 - $83,000 a year
- Full-time
- 3 years
- Bachelor's degree
- Travel

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Clinical Research Associate (CRA) – Temporary 6 Month Contract

Lighthouse Lab Services -
Waltham, MA

Quick Apply

Job Details

Temporary | Part-time | Contract
$45 an hour
4 days ago

Benefits

Flexible schedule

Qualifications

English
Driver's License

Full Job Description

Clinical Research Associate (CRA) – Temporary

Location: Waltham, MA
Schedule: Flexible hours, about 20 hours a week
Employment Type: 6 month-1 year Temporary/Contract

Pay Rate: $45/hour

Position Overview

Lighthouse Lab Services is seeking an experienced Clinical Research Associate (CRA) for a temporary opportunity in Waltham, MA. The Clinical Research Associate will be responsible for monitoring clinical studies and ensuring study execution is conducted in accordance with applicable laws, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and company standards.

The CRA will serve as a primary point of contact for assigned clinical partners and investigator sites, supporting study enrollment, monitoring, data quality, protocol compliance, and study close-out activities. This position will work closely with Regulatory Affairs and other members of the clinical study team to ensure studies are completed on time and to the required quality standards.

Responsibilities

Ensure proper conduct of clinical studies in accordance with SOPs, applicable laws, ICH/GCP guidelines, FDA regulations, and company standards.
Manage assigned operational aspects of clinical studies from study start through database lock, ensuring timelines and quality deliverables are met.
Serve as the primary point of contact for assigned clinical partners and investigator sites during study conduct.
Facilitate communication and information flow between clinical partners, investigators, vendors, and internal study team members.
Attend investigator meetings, either virtually or in person, as required.
Support patient enrollment and recruitment initiatives by identifying and addressing recruitment challenges with investigator sites.
Conduct remote/electronic monitoring activities and study close-out activities as needed.
Ensure monitoring activities are conducted in accordance with SOPs and are appropriately adjusted based on emerging study issues and technologies.
Monitor adverse events (AEs) and serious adverse events (SAEs), working with the study team to resolve outstanding issues and ensure required information is documented.
Maintain accurate and timely Trial Master File (TMF) documentation and study records.
Track and submit required reports, documentation, updates, and metrics, including protocol deviations, patient recruitment, clinical supplies, and overall study progress.
Resolve data queries and ensure close-out activities are completed within established timelines.
Ensure appropriate oversight of investigational products, including receipt, handling, accountability, storage conditions, and destruction.
Support database release activities as needed.
May perform responsibilities associated with an unblinded monitor when appropriate.
Collaborate with the Regulatory Affairs Manager and other study team members on study start-up, execution, and close-out activities.
Identify and resolve protocol-related issues to support successful study execution.

Qualifications

Bachelor's degree in a life science or related field, or a professional degree such as nursing, pharmacy, medicine, or equivalent.
Minimum of 3 years of relevant clinical research experience, including site monitoring experience.
Oncology clinical research experience preferred, with approximately 2 years of oncology monitoring experience strongly preferred.
Extensive knowledge of clinical study methodologies, ICH/GCP guidelines, and FDA regulations.
Experience with clinical site monitoring, study documentation, and clinical trial operations.
Strong organizational, communication, and problem-solving skills.
Fluent in English.
Valid driver's license required.

About us:

At Lighthouse Lab Services, we offer solutions to help start, grow, and run clinical laboratories. Our recruiting team has over 21 years of proven success placing job seekers in positions ranging from entry-level Medical Technologists to seasoned Laboratory Directors. We recruit nationwide, for permanent and travel positions with clients ranging from small hospitals to large reference laboratories.

It is the policy of Lighthouse Lab Services to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. Lighthouse Lab Services is committed to working and providing reasonable accommodation to individuals of all abilities, including persons with disabilities.

If at any time during the application process, you need an accommodation, please contact [email protected] for assistance.
Lighthouse Lab Services | 844-974-1929 | https://www.lighthouselabservices.com/

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Refine Your Search

clinical research coordinator jobs in milford, ma

Clinical Research Associate (CRA) – Temporary 6 Month Contract

Clinical Research Coordinator, Per Diem, Framingham Heart Study

Clinical Research Coordinator II

Clinical Research Assistant

Clinical Research Asst II

Clinical Research Coordinator II - Attleboro

Clinical Research Coordinator I

Clinical Research Coordinator - Open Rank

Clinical Research Coord I

Clinical Research Coordinator

Clinical Research Associate

Clinical Research Coordinator III

Administrative Coordinator - Large Animal Clinical Sciences

Clinical Research Coordinator - Cancer Genetics

Clinical Research Coordinator I - Urology

Clinical Research Coordinator II - Foxborough

Clinical Research Associate - Contract

Clinical Research Assistant I (MFM)

Clinical Trials Research Coordinator

Senior Clinical Research Coordinator - Milford

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