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Full Time Labcorp Clinical Trials Jobs (NOW HIRING)

Schweigerderm

Manager - Clinical Trials

Hackensack, NJ · On-site

$70K - $85K/yr

The Clinical Trials Manager oversees the planning, execution, and monitoring of clinical research ... Schedule: Full time, 30+ hours. Availability Monday through Friday with rotating Saturdays within ...

Vitalief

Clinical Trials Coverage Analyst

Chicago, IL · Remote

$70K - $85K/yr

THE ROLE We are seeking a full-time, fully benefited Vitalief employee to serve as a Clinical Trials Coverage Analyst in a fully remote capacity, supporting a leading academic clinical research ...

Vitalief

Clinical Trials Contracts Manager

New Brunswick, NJ · On-site +1

$91K - $122K/yr

THE ROLE We are seeking a full-time, fully benefited Clinical Trials Contracts Manager to join Vitalief in a fully remote position supporting our client, a leading academic clinical research center ...

Vitalief

Clinical Trials Contracts Manager

New Brunswick, NJ · Remote

$91K - $121K/yr

THE ROLE We are seeking a full-time, fully benefited Clinical Trials Contracts Manager to join Vitalief in a fully remote position supporting our client, a leading academic clinical research center ...

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Full Time Labcorp Clinical Trials information

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How much do full time labcorp clinical trials jobs pay per year?

As of Jul 23, 2026, the average yearly pay for full time labcorp clinical trials in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.
What cities are hiring for Full Time Labcorp Clinical Trials jobs? Cities with the most Full Time Labcorp Clinical Trials job openings:
What are the most commonly searched types of Labcorp Clinical Trials jobs? The most popular types of Labcorp Clinical Trials jobs are:
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Full Time Labcorp Clinical Trials jobs near you
Clinical Research Coordinator, Cardiovascular Device Clinical Trials

Clinical Research Coordinator, Cardiovascular Device Clinical Trials

Southcoast Health System, Inc.

Fall River, MA • On-site

$57K - $96K/yr

Full-time

Retirement

Posted 29 days ago

Southcoast Health rating

7.0

Company rating: 7.0 out of 10

Based on 75 frontline employees who took The Breakroom Quiz

417th of 889 rated healthcare providers

Job description

Overview
Community Focused. Care Driven.
Join Southcoast Health, where your future is as promising as the care we provide. Our commitment to each other, our patients, and our community is more than a mission - it's our way of life, and you'll be at the heart of it.
Southcoast Health is a not-for-profit, charitable, health system with multiple hospitals, clinics and facilities throughout Southeastern Massachusetts and Rhode Island.
Nestled in local communities, Southcoast Health provides inclusive, ethical workplaces where our highly skilled caregivers offer world-class, comprehensive healthcare close to home.
Find out for yourself why Southcoast Health has been voted 'Best Place to Work' for 7 years in a row!
We are searching for a talented Clinical Research Coordinator, Cardiovascular Device Clinical Trials
Hours: Full Time - Exempt
Shift: Day Shift
Location: Fall River, MA
A career at Southcoast Health offers you:
  • A culture of well-being that embraces, respects, and celebrates the rich diversity of one another and the communities we serve
  • Competitive pay and comprehensive benefits package
  • Generous Earned Time Off Package**
  • Employee Wellbeing Program
  • 403B Retirement Plan with company match
  • Tuition assistance / Federal Loan Forgiveness programs
  • Professional growth opportunities and customized leadership training

**Available to regular status employees who are scheduled to work a minimum of 24 hours.
Southcoast Health is an Equal Opportunity Employer.
Responsibilities
Under the direction of the Care Center Director or Designee, perform diversified duties in coordinating all activities related to clinical trials. Duties include but are not limited to oversight of all research-related activities, screening and evaluation of prospective trial patients, clinical follow-up of enrolled trial patients, correspondence and coordination with the Institutional Review Board and trial sponsors. Facilitation and development of relationships with Sponsors for clinical trials. Management/tracking of compliance with Federal and institution guidelines relating to conducting human subject research. Educate patients to clinical trials and obtain informed consent to participate. Responsible for implementing new trials, collaborating with multiple MD Principal Investigators, negotiating and maintaining budgets, managing audits and ensuring adherence to study protocols about mandated visits, medicine management and symptom tracking.
Qualifications
  • Bachelors Degree or the equivalent experience is required.
  • Degree in Healthcare administration, Healthcare, Science or related field is preferred.
  • Three to five years of experience working directly in clinical trials involving human subjects is preferred.
  • Attention to detail and strong organizational skills are required.
  • US Drivers license is required. Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Associate (CCRA) is preferred.
  • Certification within 6 months of hire.
  • If less than 2 years full time clinical research experience, the minimum allowed before you can sit for the exam, certification will then be required.
  • Must be fully vaccinated against seasonal Influenza and the COVID 19 virus or to be exempt from the requirement for medical or personal reasons by signing a statement certifying you are choosing to be exempt from vaccination once hired.
  • Compensation: Pay rate will be determined based on level of experience.

Pay Range
USD $57,553.60 - USD $96,761.60 /Yr.

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