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Clinical Contracts Jobs (NOW HIRING)

Clinical Contracts Analyst (REMOTE)

Boston, MA · Remote

$75K - $90K/yr

Position Summary The Clinical Contracts Analyst will develop and negotiate contracts and budgets associated with clinical trials, ensure contracts comply with regulations, manage the lifecycle of ...

Clinical Contracts Analyst (REMOTE)

Philadelphia, PA · On-site +1

$69K - $84K/yr

Position Summary The Clinical Contracts Analyst will develop and negotiate contracts and budgets associated with clinical trials, ensure contracts comply with regulations, manage the lifecycle of ...

As a Clinical Contract Analyst, you will play a critical role in enabling clinical operations by driving contract management, vendor coordination, and financial processes that support both clinical ...

$170 - $182/hr

The Senior Manager, Clinical Contracts will ensure the successful negotiation and ongoing management of clinical trial-related agreements and serve as the key liaison between Clinical Operations ...

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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:

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.

Sr. Clinical Outsourcing Contracts Manager

Neurocrine Biosciences

San Diego, CA • On-site

$148.50 - $203/hr

Other

Medical, Dental, Vision, Retirement, PTO

Re-posted 3 hours ago


Job description

About the Role

Responsible for leading the development of clinical site budgets, review, adjustment and negotiation with clinical sites, and for ensuring contracts are executed timely. Manages the administrative execution of clinical contracts across multiple projects, coordinates with Accounting and legal teams, and may supervise contract administrators.

Your Contributions
  • Manages clinical trial contractual negotiations, triaging, reviewing and escalating issues across multiple projects.
  • Ensures on‑time processing of all clinical contracts from initial request through execution in accordance with project timelines.
  • Attends clinical operational meetings to advise on contracting activities across multiple projects and vendors.
  • For outsourced studies, manages CRO contracts, site and budget agreement activities, and serves as primary contact and budget liaison between CRO, company legal and clinical operations.
  • Oversees the CTA start‑up process, including development and routing of CTA templates, budget grids and supporting documentation to sites.
  • Serves as escalation contact with sites for contracts and coordinates web requests and legal execution of CTAs.
  • Collaborates with the Head of Clinical Operations in managing work orders, service agreements, consulting agreements, license agreements, MSAs and CDAs.
  • Guides budget negotiation with clinical sites based on parameters defined by the Head of Clinical Operations.
  • Collaborates with finance/accounting departments to support contract budgets and monthly/quarterly reviews.
  • Manages invoices associated with clinical trials and ensures payments are made based on executed contracts.
  • Contributes to process efficiencies and organization of contracting and budget/payment processes.
  • Mentors and delegates cross‑functionally to support growth of direct reports.
  • Leads onboarding for clinical contracts personnel.
  • Performs other duties as assigned.
Requirements
  • BS/BA degree in business administration or health care/science related field AND 8+ years of experience in a CRO, Biotech or Pharmaceutical organization.
  • OR Master’s degree in business administration or health care/science related field AND 6+ years of similar experience in contract management, negotiation, budgeting and administration.
  • Anticipates business and industry issues; recommends process, technical or service improvements.
  • Demonstrates broad expertise and is considered an expert within the company, with external presence in the area of expertise.
  • Applies in‑depth expertise and broad knowledge of related areas to improve team efficiency.
  • Leads and collaborates with multiple teams; strong leadership and mentoring skills.
  • Excellent computer, communication, problem‑solving, analytical thinking and project management skills.
  • Ability to meet multiple deadlines across a variety of projects with high accuracy and efficiency.
  • Expert at managing complexity and multiple work streams in changing circumstances.
  • Advanced knowledge of the clinical trial process, regulations and guidelines; proven success across a matrix organization.
  • Demonstrated ability to prepare and negotiate external provider master service agreements, work/change orders, etc., and track them for clinical operations.
  • Can read and interpret highly complex clinical contracts to ensure language/terms meet company standards.
  • Expert contract administration skills, including managing budgets, billing/invoicing, issue resolution and acting as CRO point of contact.
  • Advanced understanding of clinical contract accounting and budgeting processes.
  • Advanced understanding of drug development and clinical operations.
Compensation & Benefits

The annual base salary ranges from $148,500.00 to $203,000.00, with pay decisions based on location, complexity, responsibilities, job duties and experience.

Additional compensation includes an annual bonus target of 30% of the earned base salary and eligibility for a company equity‑based long‑term incentive program.

Benefits include a retirement savings plan with company match, paid vacation, holiday and personal days, paid caregiver/parental leave, medical leave, and health benefits covering medical, prescription drugs, dental and vision.

EEO & Diversity Statement

Neurocrine Biosciences is an EEO/Disability/Vets employer. We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements.

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