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Clinical Trials Contracts Manager Jobs (NOW HIRING)

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 ...

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 ...

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 ...

... all trials within the portfolio, escalating concerns and issues to the HRI operational and ... Manager is the facilitator for clinical communication between the program, leadership, and the ...

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Clinical Trials Contracts Manager information

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$41K

$106K

$139K

How much do clinical trials contracts manager jobs pay per year?

As of Aug 7, 2026, the average yearly pay for clinical trials contracts manager in the United States is $106,034.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,000.00 and $119,000.00 per year, depending on experience, location, and employer.

What is a clinical trials contracts manager?

A Clinical Trials Contracts Manager is a professional responsible for negotiating, drafting, and managing contracts between sponsors, research institutions, and other parties involved in clinical trials. They ensure that all agreements comply with regulatory requirements and protect the interests of their organization. Their role involves coordinating with legal, finance, and clinical teams, managing timelines, and resolving any contract-related issues that arise during the course of a clinical trial.

How does a clinical trials contracts manager collaborate with legal, clinical, and sponsor teams during contract negotiation?

A Clinical Trials Contracts Manager works closely with legal departments to ensure compliance with regulatory requirements and institutional policies while drafting and negotiating contracts. They also coordinate with clinical teams to understand study protocols and operational needs, ensuring contract terms align with trial objectives. Regular communication with sponsors is essential to clarify expectations, resolve budget or indemnification concerns, and expedite contract execution. This cross-functional collaboration helps streamline the contracting process and supports timely study start-up.

What skills and qualifications are needed to be a clinical trials contracts manager?

To thrive as a Clinical Trials Contracts Manager, you need a solid understanding of clinical research, contract law, and negotiation, typically supported by a degree in life sciences, law, or a related field. Familiarity with clinical trial management systems (CTMS), contract management software, and regulatory guidelines such as ICH-GCP is essential. Strong organizational skills, attention to detail, and effective communication with stakeholders set top performers apart. These skills ensure compliance, timely contract execution, and successful collaboration among research teams and sponsors.

What is the difference between Clinical Trials Contracts Manager vs Clinical Research Coordinator?

AspectClinical Trials Contracts ManagerClinical Research Coordinator
Primary RoleManages contract negotiations and legal agreements with sponsors and sitesOversees daily trial operations, patient recruitment, and data collection
Required CredentialsBachelor's degree, experience in contracts, knowledge of regulationsBachelor's degree, clinical research experience, good clinical practice (GCP) knowledge
Work EnvironmentLegal, administrative, and compliance-focused settingsClinical sites, hospitals, or research centers
Industry UsageCommon in pharmaceutical and biotech companiesCommon in hospitals, research institutions, and CROs

The Clinical Trials Contracts Manager primarily handles contract negotiations and legal aspects of trials, requiring legal and regulatory knowledge. In contrast, the Clinical Research Coordinator focuses on trial operations and patient management. Both roles are essential in clinical research but serve different functions within the trial process.

More about Clinical Trials Contracts Manager jobs
What cities are hiring for Clinical Trials Contracts Manager jobs? Cities with the most Clinical Trials Contracts Manager job openings:
What states have the most Clinical Trials Contracts Manager jobs? States with the most job openings for Clinical Trials Contracts Manager jobs include:
What job categories do people searching Clinical Trials Contracts Manager jobs look for? The top searched job categories for Clinical Trials Contracts Manager jobs are:
Infographic showing various Clinical Trials Contracts Manager job openings in the United States as of August 2026, with employment types broken down into 95% Full Time, and 5% Part Time. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $106,034 per year, or $51 per hour.

Clinical Trials Assistant

Quakertown Veterinary Clinic

Quakertown, PA • On-site

Part-time

Re-posted 5 days ago


Job description

This is a part-time position that could go into full-time


Clinical Trials Assistant
Summary

The Clinical Trials Assistant supports the clinical research team by helping identify veterinary patients who may be eligible for approved clinical trials. Working alongside veterinarians and the research team, this role reviews scheduled appointments, laboratory results, and medical records to help identify potential study candidates for further evaluation by the clinical trials team.

This position also provides administrative and clinical support for ongoing research studies while assisting with patient care in a veterinary hospital setting. The role offers opportunities to learn research procedures and clinical trial operations through training and hands-on experience.

Essential Duties and Responsibilities
  • Perform all duties in accordance with hospital policies, study protocols, and applicable regulations.
  • Prepare and maintain examination rooms and treatment areas.
  • Review upcoming patient appointments and medical information to identify patients who may meet study eligibility criteria.
  • Notify the clinical trials team of potential study candidates for review by the study veterinarian or investigator.
  • Maintain familiarity with active clinical trials and their eligibility requirements.
  • Support Good Clinical Practice (GCP) standards in the conduct of research studies.
  • Assist veterinarians and study personnel during appointments and research visits.
  • Learn and follow study protocols and electronic data capture systems.
  • Communicate professionally with pet owners regarding approved clinical studies and protocol-required follow-up.
  • Coordinate with study sponsors, contract research organizations, and research partners as directed.
  • Maintain study supplies, investigational products, and inventory records.
  • Participate in required training related to clinical research and hospital procedures. (Required training is compensated.)
  • File study documentation, resolve data queries, and assist with maintaining accurate research records.
  • Prepare laboratory samples for shipment according to study requirements.
  • Under appropriate training and supervision, assist with administering medications and treatments as permitted by hospital policy and applicable regulations.
  • Under supervision, assist with collecting diagnostic samples and performing basic laboratory procedures.
  • Under supervision, assist with obtaining diagnostic images and non-invasive patient measurements.
  • Assist with patient admissions and discharges and provide client education as directed by the veterinary team.
  • Learn about commonly prescribed medications, preventatives, and therapeutic diets to assist with client education.
  • Support other hospital team members as needed.
  • Maintain accurate medical and research records.
  • Provide compassionate, professional care to patients and exceptional service to clients.
  • Maintain professional appearance and conduct.
  • Perform other duties as assigned.
Preferred Qualifications
  • High school diploma or equivalent required.
  • College coursework, associate's degree, bachelor's degree, or Certified Veterinary Technician (CVT) credential preferred but not required.
  • Previous veterinary hospital, animal care, or clinical research experience is preferred.
Skills and Competencies
  • Strong communication and interpersonal skills.
  • Excellent organizational skills and attention to detail.
  • Ability to prioritize tasks in a fast-paced environment.
  • Strong teamwork and collaboration skills.
  • Professional customer service skills.
  • Ability to remain calm and efficient in busy clinical settings.
  • Passion for animal health and patient care.
  • Basic computer proficiency; experience with veterinary practice management software is a plus.
Computer Skills

Experience with Microsoft Office is preferred. Familiarity with veterinary practice management software, including Impromed or similar systems, is beneficial but not required.

Travel

Minimal travel may occasionally be required.

Physical Requirements

This position requires frequent standing, walking, bending, lifting, and speaking. Employees should be able to routinely lift up to 40 pounds and occasionally assist with lifting larger animals with team assistance.

Work Environment

Work is performed in a veterinary hospital and clinical research setting. Employees may be exposed to anesthetic gases, animal odors, noise, blood and other biological materials, animal waste, contagious diseases, and the risk of animal bites or scratches. Appropriate training and personal protective equipment are provided in accordance with hospital policies.