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Clinical Trial Contract Jobs (NOW HIRING)

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$75K - $90K/yr

... 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 ...

PTC Therapeutics

Contract, Clinical Trial Associate

Warren, NJ · On-site

$34.75 - $47.50/hr

The Contract, Clinical Trial Associate provides clinical study and Trial Master File (TMF) support for clinical operations. This involves supporting Clinical Trial Managers (CTMs) with activities ...

Viking Therapeutics

Clinical Trial Manager

San Diego, CA · On-site

$110K - $140K/yr

Supports all aspects of clinical trial management and processes from initiation, planning ... Experience negotiating vendor/site contracts and managing the budgets * Solid vendor management ...

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 ...

Sagimet Biosciences

Clinical Trial Manager

San Mateo, CA · On-site

$90 - $100/hr

Job Type Contract Description The Clinical Trial Manager manages and leads the day-to-day clinical trial activities related to the development and execution of cross-functional and third-party vendor ...

Kardigan

Clinical Trial Manager

Princeton, NJ · On-site

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 ...

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All JobsClinical Trial Contract Jobs

Clinical Trial Contract information

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$11

$37

$68

How much do clinical trial contract jobs pay per hour?

As of Jul 29, 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 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 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 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 July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.
Clinical Trial Associate II

Clinical Trial Associate II

Prometrika LLC

Cambridge, MA • On-site

$75K - $90K/yr

Full-time

Posted 29 days ago

Job description

PROMETRIKA is a full-service clinical research organization (CRO) with extensive experience in clinical operations, data management, biostatistics, medical writing, and pharmacovigilance. We’re driven by our passion for the human aspect of our work and our compassion for the people whose lives have been improved by the innovations we help bring to market. Our clients include national and international biopharmaceutical and medical device companies of all sizes.

The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research projects, working with the study team in the initiation, maintenance and closeout of clinical projects according to GCP, ICH, CFR and SOPs/WPDs. The CTA II will:

  • With minimal oversight, manage all study start up, maintenance and closeout site management responsibilities, under the supervision of the Clinical Trial Manager
  • Lead the maintenance of audit-ready clinical trial documentation and study status: manage and track regulatory documentation, IND Safety Letter distribution, Confidentiality Agreements and Clinical Trial 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, develop study specific processes to ensure that necessary study supplies are available at sites as required, coordinating with appropriate vendors as needed (i.e., Case Report Forms, Study Manuals, lab kits, drug supplies, lab supplies, etc.)
  • With minimal oversight, manage clinical operations site payments, prepare site invoices and supporting documentation, and approve site payment distribution
  • With minimal oversight, manage drug supply and non-drug supply study trackers
  • May assist with reviewing monitoring visit reports

The CTA II will also perform the following CTA responsibilities:

  • Support the CTM or project manager with study start up and execution
  • Act as a second point of contact between team members, vendors and study sites to assist with study conduct
  • Follow established clinical study standards and procedures to plan and conduct clinical research studies
  • Request, collect and submit site documents
  • Review study start up documents and disseminate to the appropriate functional groups (i.e., legal, regulatory)
  • Coordinate IRB/EC submissions and tracking progress to review and approval
  • Track study start-up status
  • Support the establishment and maintenance of the study TMF. Prepare master Clinical Study Files and Trial Master Files for archiving and/or transfer to a client
  • Set-up and maintain study clinical trial management system (CTMS)
  • Assist in development of supportive study documents such as informed consent forms, monitoring templates, study subject tracking tools, study drug shipment and monitoring forms, study manuals and training materials, as required for a new clinical study
  • Assist with and/or may play a lead role in the development of data collection tools and procedure manuals
  • Work with Project Managers/ Clinical Trial Manager to develop status report templates in accordance with client specifications. Assists the Project Managers/ Clinical Trial Manager to compile status report data throughout the course of a study
  • Assist with the tracking and compilation of enrollment information from sites
  • Participate in tracking and reporting of study data for management reports
  • Collate and distribute study related materials
  • Collate and assemble study binders (regulatory, pharmacy, laboratory), study reference manuals and study data collection tools
  • Support non-drug supply management
  • Support clinical operations site payments, prepare site invoices and supporting documentation
  • Accompany the CTM or CRA on site monitoring visits, if required
  • Will have some site management responsibilities
  • Assist with vendor management
  • Apply knowledge of company policies and standard practices to resolve problems
  • Maintain open communication channels with study sites and members of the study team to ensure proper study progress
  • Analyze issues and use judgment to make decisions
  • Escalate non-standard problems or issues as may be required
  • Contribute to Standard Operating Procedures (SOPs), manuals, forms and templates to support efficient and compliant best practices of the department
  • Contribute to thought leadership and knowledge sharing activities
  • Lead team trainings
  • Continually identify, recommend and implement innovative process ideas and technologies to elevate PROMETRIKA’s core competencies and offerings
  • Perform other duties as required

EDUCATION

  • Bachelor’s degree in a scientific or health related field or equivalent
  • PMP Certification preferred but not required

EXPERIENCE

  • Minimum of 2 years of experience directly supporting clinical research trials

SKILLS

  • Problem solving abilities, troubleshooting abilities and resourcefulness
  • Analytical problem-solving experience, including excellent organizational skills and attention to detail
  • Working knowledge of clinical drug development process as well as ICH, GCP guidelines, and US FDA regulations
  • Effective communication and interpersonal skills; ability to build relationships internally and externally
  • Knowledge seeking personality, interested in continually seeking out new information, techniques and diverse perspectives
  • Ability to track many actions and prioritize timely completion
  • Cross functional and cross-cultural awareness, someone who seeks out diverse perspectives and considers these perspectives in decisions that are made
  • Must possess soft skills and empathy towards others
  • Patient centric philosophy towards research is a must
  • Familiarity with medical terms
  • Demonstrated writing skills to deliver messages effectively so messages are clearly understood
  • Demonstrated expertise with PCs and standard Microsoft Office software applications

Physical Requirements

Incumbents generally must be able to, with or without accommodation, have the proficient use of both sensory perception/clarity and muscle control/coordination. This may include vision (near, far, color, glare control), hearing (auditory attention, sound localization), speech, strength, agility, dexterity flexibility, steadiness or reaction time.


The salary range for this position here noted is representative of a good faith estimate of all experience levels for this position. PROMETRIKA considers several factors when extending and offer, including but not limited to the role, the function and associated responsibilities, the candidate’s work experience, education/training background and parity with current employees in the same or similar positions.