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Clinical Contracts Jobs (NOW HIRING)

Tekhawks LLC

Be Seen First

Sr. Clinical Contracts Associate - Plano, TX or Maple Grove, MN

Plano, TX · On-site

$45 - $55/hr

Job Title: Sr. Clinical Contracts Associate Duration: 12+ Months Location: Plano, TX or Maple Grove, MN Position Overview Seeking a Clinical Contracts Associate to support the development ...

Tekhawks LLC

Be Seen First

Sr. Clinical Contracts Associate - Plano, TX or Maple Grove, MN

Plano, TX · On-site

$45 - $55/hr

Job Title: Sr. Clinical Contracts Associate Duration: 12+ Months Location: Plano, TX or Maple Grove, MN Position Overview Seeking a Clinical Contracts Associate to support the development ...

Abbott

Clinical Contracts Associate II

Plano, TX · On-site

Clinical Contract Associatepositionwith Sylmar, CA, Santa Clara, CA, Plano, TXor Maple Grove, MN as preferred location. This is an in-office position Position Summary Working under the direction of ...

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Clinical Contracts information

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$41K

$106K

$139K

How much do clinical contracts jobs pay per year?

As of Aug 22, 2026, the average yearly pay for clinical contracts 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 are clinical contracts?

Clinical contracts are legally binding agreements that outline the terms and conditions for conducting clinical trials or research studies. These contracts typically detail the responsibilities, obligations, timelines, and financial arrangements between sponsors, research sites, investigators, and other parties involved in the study. Clinical contracts help ensure compliance with regulatory requirements, protect the interests of all parties, and clarify the scope of work and confidentiality. They play a crucial role in facilitating smooth collaboration and minimizing risks during clinical research.

What are the key skills and qualifications needed to thrive as a clinical contracts specialist?

To thrive as a Clinical Contracts Specialist, you need a solid understanding of clinical research, contract negotiation, and legal terminology, typically supported by a bachelor’s degree in life sciences, business, or law. Familiarity with contract management systems, regulatory compliance tools, and Microsoft Office Suite is commonly required. Strong attention to detail, negotiation skills, and effective communication are crucial soft skills for managing complex agreements and facilitating collaboration. These competencies ensure that clinical trials proceed smoothly, legally compliant, and within budget and time constraints.

What are some common challenges faced by professionals in clinical contracts, and how can they be effectively managed?

Professionals in Clinical Contracts often encounter challenges such as negotiating complex terms with multiple stakeholders, managing tight timelines, and ensuring compliance with regulatory requirements. Effectively managing these challenges involves strong communication skills to align expectations, attention to detail to avoid contractual risks, and staying updated on industry regulations. Building collaborative relationships with legal, finance, and clinical operations teams also helps streamline the contract review and approval processes.

What is the difference between Clinical Contracts vs Clinical Research Associate?

AspectClinical ContractsClinical Research Associate
Primary RoleDrafting, negotiating, and managing clinical trial contracts with vendors, sites, and partnersMonitoring clinical trial progress, ensuring compliance, and collecting data at trial sites
Required CredentialsLegal or contractual background, often with life sciences knowledgeLife sciences degree, clinical research certifications
Work EnvironmentLegal, legal teams, or contract management departmentsClinical sites, research teams, monitoring visits
Industry UsageLegal and contractual departments within pharmaceutical or biotech companiesClinical research organizations, pharmaceutical companies, CROs

While Clinical Contracts focus on managing agreements related to clinical trials, Clinical Research Associates are involved in monitoring and ensuring the quality of clinical trial conduct. Both roles are essential in the clinical research process but serve different functions within the industry.

More about Clinical Contracts jobs

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

The most popular types of Clinical Contracts jobs are:

What states have the most Clinical Contracts jobs?

States with the most job openings for Clinical Contracts jobs include:

What job categories do people searching Clinical Contracts jobs look for?

The top searched job categories for Clinical Contracts jobs are:

Clinical Contracts jobs near you
Infographic showing various Clinical Contracts job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $106,034 per year, or $51 per hour.

Manager, Clinical Contracts & Finance - III

Fladger Associates

Foster City, CA • On-site

$103K - $138K/yr

Contractor

Re-posted 12 days ago

Job description

Foster City, CA
Contract Duration: 12-18 months
Rate: Negotiable

Responsibilities:

  • Excellent employment opportunity for a Manager, Clinical Contracts & Finance III in the Foster City, CA area.
  • Manager, Development Business Operations, ISR/Collaborative
  • Position will be accountable for the drafting, negotiation, and review of global Investigator Sponsored Research (ISR), Collaborative, and related ancillary contracts such as amendments (together referred to as "ISR/CO contracts") including both language and budget, the management of Functional Service Providers (FSPs) involved in the contracting process.
  • Will require oversight of contract activities for multiple clinical development and Medical Affairs programs within the various Company therapeutic areas, ensuring Company Contract Managers and FSP provide adequate level of staff to complete contracts in an accurate, consistent, and timely manner.
  • Must coordinate with the FSPs, the ISR/CO team, Company Clinical Operations and Company Legal departments to manage and complete the site contract process throughout study duration.
  • Responds and resolves complex issues associated with domestic and international contracts with support from more senior staff and Company Legal department.
  • Ideal candidate will have demonstrated success in working collaboratively with stakeholders, especially senior Development Business Operations management.
  • This role can manage the day-today activities in complex ISR/CO contracts and milestone review.
  • Focuses on ISR/CO contracts, amendments, and accountability as it relates to FSP management and site start-up.
  • Works with Functional Service Provider (FSP) to implement ISR/CO contracts Process to ensure efficient delivery of fully executed contracts and amendments.
  • Manages the day-to-day activities of multiple areas in moderately complex clinical contracts and finance.
  • Including but not limited working closely with internal clinical operations and Medical Affairs.
  • Engages in regular, professional communication with stakeholders, including Medical Affairs, to ensure timely negotiations and transparency of negotiation process.
  • Evaluates contract and budget changes requested within ISR/CO contracts and identifies business and/or legal risks manage the issue to resolution by proposing and providing alternative solutions to legal or senior management.
  • Identifies issues/problems and provides recommendations for solutions.
  • Assists other staff in resolving moderately complex issues relating to contract negotiation and management.
  • Ability to develop use spreadsheets and tracking tools.
  • Manages relationships in conjunction with the Clinical Operations as it relates to ISR/CO contracts
  • With the support of internal customers and the legal department, understands and leads the contract negotiation process.
  • Leads the contract life cycle management process for assigned ISR/CO contracts portfolio.
  • Demonstrates excellent verbal, written, and interpersonal communication skills.
  • This role demonstrates an in-depth knowledge of negotiations of ISR/CO contracts, and proficiency in clinical trials agreements.
  • Demonstrates strong understanding of regulatory and legal issues pertinent to clinical development and Medical Affairs.
  • Demonstrates an understanding of the regulatory implications of contracts as related to clinical research.
  • This role must be able to interact on high level with the clinical teams, and project management to provide oversight of negotiations of ISR/CO contracts and related documents.
  • Completes tasks and projects under minimal to no supervision.

Experience:

  • 5+ years of experience with a BA in a relevant discipline.
  • 3+ years of experience with a MS/MBA/JD in a relevant discipline.
  • Relevant experience typically includes contract negotiation
  • Competent in computer skills (Microsoft Office including Excel, Word and PowerPoint)
  • Relevant experience typically includes contract language and budget negotiation, and application of project management principles.
  • Global Site Contracting experience and/or ISR/CO contracts experience a plus.
  • Skilled at Project Management, able to meet deadlines on multiple concurrent projects and work collaboratively with and through others.