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Contract Remote Clinical Trials Jobs (NOW HIRING)

Vitalief

Clinical Trials Contracts Manager

New Brunswick, NJ · On-site +1

$91K - $122K/yr

... remote position supporting our client, a leading academic clinical research center in New Jersey ... The ideal candidate will bring extensive experience in clinical research contract review and ...

Vitalief

Clinical Trials Contracts Manager

New Brunswick, NJ · Remote

$91K - $121K/yr

... remote position supporting our client, a leading academic clinical research center in New Jersey ... The ideal candidate will bring extensive experience in clinical research contract review and ...

Yale University

Clinical Trials Project Manager

This is a remote position. Job seekers who live within one of Yale's approved work states are ... Contract Research Organizations (CROs) to resolve site-level barriers to activation and improve ...

CG Oncology, Inc.

Senior Clinical Trials Scientist

$150K - $170K/yr

Remote Essential Functions * Provide scientific leadership for the planning, design, and ... applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.

Gilead Sciences, Inc.

Clinical Trials Manager

$133K - $172K/yr

As a Clinical Trials Manager at Gilead/Kite, you will be responsible for: * Coordinating and ... budget/contract process. * May be asked to train CROs, vendors, investigators, and study ...

Vitalief

Clinical Trials Coverage Analyst

Chicago, IL · On-site +1

$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 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 ...

Emerald Clinical Trials

Project Specialist

$60K - $76K/yr

At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO ... Enjoy hybrid or remote working arrangements, depending on your location and role. • Career Growth

Dana-Farber Cancer Institute

Monitoring will be performed through a combination of remote data review and onsite monitoring visits; therefore, a willingness and ability to travel occasionally is required. The Clinical Trials ...

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How much do contract remote clinical trials jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for contract remote clinical trials in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.
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Contract Remote Clinical Trials jobs near you
Infographic showing various Contract Remote Clinical Trials job openings in the United States as of June 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trials Contracts Manager

Vitalief

New Brunswick, NJ • On-site, Remote

$91K - $122K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 15 days ago

Job description

ABOUT VITALIEF
Vitalief is a consulting and professional services firm that partners with clinical research sites, sponsors, and CROs to improve trial activation, operational performance, and workforce readiness. By combining clinical research expertise with operational and business excellence, we help organizations streamline processes, reduce costs, accelerate timelines, and enhance patient outcomes.
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 in New Jersey. The ideal candidate will bring extensive experience in clinical research contract review and negotiation, along with a strong understanding of regulatory, legal, and operational requirements. In this role, you will develop and sustain strategic partnerships with industry sponsors while ensuring the timely and effective review, negotiation, and management of clinical trial agreements and related research contracts.
WHY VITALIEF?
  • Work remotely while supporting high-impact clinical trials.
  • Standard work hours: 8:00am to 4:30pm EST zone.
  • Contribute to advancing scientific discoveries that improve patient lives.
  • PEOPLE FIRST culture with opportunities for growth and innovation.
  • Competitive benefits include 20 PTO days + 9 paid holidays; Company-paid life insurance and short/long-term disability; 401(k) retirement program; Comprehensive healthcare plans.
  • Market-competitive salary: commensurate with experience.

KEY RESPONSIBILITIES
  • Independently review, interpret, negotiate, and process clinical trial agreements, nondisclosure agreements, and related contracts from legal, business, and technical perspectives, ensuring alignment with institutional policies and sponsor requirements.
  • Develop and execute negotiation strategies that align with institutional policies, regulatory requirements, and sponsor expectations.
  • Provide guidance on contract terms, risk assessment, and industry best practices.
  • Collaborate with General Counsel, Risk Management, Research Commercialization, finance, and other internal stakeholders to resolve legal and business matters.
  • Maintain proactive communication with sponsors and internal teams, providing timely updates and resolving contractual issues.
  • Ensure contract packages are complete, accurate, and properly maintained, including electronic files and negotiation histories.
  • Support timely study start-up by coordinating executed agreements and distributing required documentation upon SRB approval.
  • Serve as a subject matter expert in clinical research contract management and maintain compliance with institutional, federal, and state regulations.
  • Participate in performance improvement initiatives and ongoing training to remain current on regulatory and institutional requirements.

QUALIFICATIONS
  • Bachelor's degree in Paralegal Studies, Law, or related field required; JD preferred.
  • Minimum of 3 years of clinical trial agreement review and negotiation experience, including at least 2 years within an academic medical research environment.
  • Demonstrated experience negotiating both industry-sponsored and non-industry clinical trials.
  • Strong knowledge of clinical research regulations and institutional policy frameworks.
  • Excellent written and verbal communication skills, with the ability to convey complex information clearly and effectively.
  • Proven ability to manage multiple priorities independently, exercise sound judgment, and collaborate effectively across departments.
  • Detail-oriented, proactive, and committed to delivering exceptional customer service.

PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs.
IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.
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