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Clinical Trial Contract Jobs (NOW HIRING)

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

The CTLis responsible forcoordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelinesand withquality.

Allucent

Clinical Trial Lead

Cary, NC · On-site +1

The CTL is responsible for coordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelines and with quality.

Allucent

Clinical Trial Lead

Cary, NC · Remote

The CTL is responsible for coordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelines and ...

Medpace, Inc.

Experienced Contract Manager

Irving, TX · On-site +1

$82K - $110K/yr

Experience with clinical trial contracting or life sciences commercial operation Travel : minimal Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing ...

Medpace, Inc.

Contract Manager

Cincinnati, OH · On-site +1

$85K - $114K/yr

Experience with clinical trial contracting or life sciences commercial operation Travel : minimal Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing ...

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$36.50 - $50/hr

... Contracts, as well as other clinical trial documents * Set-up, implement and maintain the audit-ready eTMF system under guidance of the Clinical Trial Manager * In collaboration with the Sr. CTA/CTM ...

Ora

Sr. Site Contract and Payment Associate

Support the development and , review, and negotiate clinical trial budgets with sponsors and sites, including per-patient costs, start-up fees, pass-through expenses, and overhead * Track contract ...

Ora

Sr. Site Contract and Payment Associate

Support the development and , review, and negotiate clinical trial budgets with sponsors and sites, including per-patient costs, start-up fees, pass-through expenses, and overhead * Track contract ...

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ

$95K - $115K/yr

Minimum of 2 years of progressive experience in clinical operations, clinical trial management, or project management within the pharmaceutical, biotechnology, medical device, or contract research ...

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... Manages CRO and vendor budgets and invoicing procedures according to study contract * Summarizes ...

Icon plc

Clinical Trial Manager

Raleigh, NC · On-site

Manage clinical trial budget and associated vendor contracts, including tracking and data in associated systems * Ensure quality and completeness of TMF for assigned clinical trials * Participates in ...

Icon plc

Clinical Trial Manager

Houston, TX · On-site

Manage clinical trial budget and associated vendor contracts, including tracking and data in associated systems * Ensure quality and completeness of TMF for assigned clinical trials * Participates in ...

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Clinical Trial Contract information

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$11

$37

$68

How much do clinical trial contract jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for clinical trial contract in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What are clinical trial contracts?

Clinical trial contracts are legally binding agreements between sponsors (such as pharmaceutical companies) and research institutions or investigators that outline the terms and conditions for conducting a clinical trial. These contracts specify responsibilities, financial arrangements, intellectual property rights, confidentiality, publication rights, and regulatory compliance. They play a crucial role in ensuring that both parties understand their obligations, protect participants’ rights, and comply with ethical and legal standards throughout the research process.

What are the key skills and qualifications needed to thrive as a clinical trial contract specialist, and why are they important?

To thrive as a Clinical Trial Contract Specialist, you need a solid understanding of contract law, clinical research regulations, and strong negotiation skills, typically supported by a degree in life sciences, law, or a related field. Familiarity with contract management systems, regulatory databases, and Microsoft Office Suite is commonly required, along with certifications such as CCRA or CCTM being advantageous. Attention to detail, strong communication, and problem-solving abilities are crucial soft skills that distinguish top performers in this role. These competencies ensure accurate, compliant, and timely contract execution, which is vital for the smooth and ethical operation of clinical trials.

What are some common challenges faced by professionals working in clinical trial contract roles, and how can they be addressed?

Professionals in clinical trial contract roles often encounter challenges such as negotiating complex legal terms, aligning diverse stakeholder interests, and ensuring compliance with regulatory requirements. Navigating differences between sponsor and site requirements or timelines can also be demanding. To address these challenges, effective communication, strong negotiation skills, and a thorough understanding of clinical research regulations are essential. Collaborating closely with legal teams, clinical operations, and external partners helps streamline the process and facilitates faster contract finalization.

What is the difference between Clinical Trial Contract vs Clinical Research Associate?

AspectClinical Trial ContractClinical Research Associate
Primary RoleDrafting, negotiating, and managing contracts with sites and vendorsMonitoring clinical trial sites, ensuring protocol compliance
Required CredentialsLegal, regulatory, or contract management background often with life sciences knowledgeLife sciences degree, clinical research certifications (e.g., CCRP)
Work EnvironmentLegal, contractual, and administrative settingsClinical sites, hospitals, or research organizations
Industry UsageUsed mainly in contract negotiations and management teamsCommonly employed in clinical trial monitoring teams

While both roles are integral to clinical trials, a Clinical Trial Contract focuses on legal agreements and negotiations, whereas a Clinical Research Associate primarily monitors trial progress and compliance at research sites.

What cities are hiring for Clinical Trial Contract jobs?

Cities with the most Clinical Trial Contract job openings:

What are the most commonly searched types of Clinical Trial jobs?

The most popular types of Clinical Trial jobs are:

What states have the most Clinical Trial Contract jobs?

States with the most job openings for Clinical Trial Contract jobs include:

Clinical Trial Contract jobs near you
Infographic showing various Clinical Trial Contract job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Clinical Trial Lead

Allucent

Cary, NC • On-site, Remote

Full-time

Re-posted 12 days ago

Job description

At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

We are looking for a Clinical Trial Leader (CTL) to join our A-team (office-based*/remote). As a CTL at Allucent, you are providing leadership, management and oversight to the Clinical Research Associates (CRAs) and other clinical functional groups, in their day-to-day clinical trial activities on a global, multi-country, or regional basis. The CTLis responsible forcoordinating and managing the planning, implementation, tracking, and ensuring the clinical deliverables as per the trial contract, budget, timelinesand withquality.

Responsibilities

As an expert in Clinical Trial Leadership, you are:

  • Coordinating and managing CRA activities across all geographies, liaising with sponsor and Project Managerand other functional leadsto ensureclinical monitoringdeliverables (timeline, budget, quality, productivity) are met.
  • Liaising closely with the Project Manager (PM) and other department leaders if /whennecessary,on all trial-related issues and service delivery.
  • Supporting the management team with training, process improvements, co-monitoring visits,mentoring ofstaffand /or any other special assignments within Global Clinical Operations.

Requirements

To be successful you will possess:

  • A degree in life sciences or nursing qualification preferred, but notrequired.
  • A minimum of5years ofclinical research experience with at least2-years'CTL or other relevant experience.
  • In-depth knowledge ofICH GCP,clinicaltrialsand the critical elements for success in clinical trials 
  • Strong therapeutic background in oncology
  • Possesses experience and knowledge in the CRO industry that will supportAllucent'smanagement of clinical trials
  • Strong written and verbal communication skills including professional command of English language to communicate with internal and external stakeholders on a daily basis.

Benefits

Benefits of working at Allucent include:

  • Comprehensive benefits package per location
  • Competitive salaries per location
  • Departmental Study/Training Budget for furthering professional development
  • Flexible Working hours (within reason)
  • Opportunity for remote/hybrid* working depending on location
  • Leadership and mentoring opportunities
  • Participation in our Buddy Program as a new or existing employee
  • Internal growth opportunities and career progression
  • Financially rewarding internal employee referral program

Disclaimers:

*Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.

"The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively "Allucent"). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources."

#LI-Remote #LI-Hybrid #LI-TCW

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