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Clinical Contracts Associate Jobs (NOW HIRING)

Tekhawks LLC

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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

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 ...

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 ...

Integrated Resources

Administrative Assistant

Cambridge, MA · On-site

$19.75 - $26.50/hr

... Contracts Associates. The Contracts Assistant will liaise with both internal and external stakeholders as required in the execution and document management of clinical contracts, management of ...

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Clinical Contracts Associate information

See salary details

$15

$36

$54

How much do clinical contracts associate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical contracts associate in the United States is $36.34, according to ZipRecruiter salary data. Most workers in this role earn between $26.44 and $43.75 per hour, depending on experience, location, and employer.

What is a clinical contracts associate?

Clinical Contracts Associates are professionals who manage and negotiate contracts related to clinical trials and research studies, typically within the pharmaceutical, biotechnology, or healthcare industries. They ensure that agreements with research sites, vendors, and other stakeholders are compliant with legal, regulatory, and company requirements. Their responsibilities often include drafting, reviewing, and revising contracts, as well as collaborating with legal, finance, and clinical operations teams. Clinical Contracts Associates play a crucial role in supporting the timely initiation and execution of clinical studies.

What are some common challenges a clinical contracts associate faces when negotiating agreements with clinical trial sites?

Clinical Contracts Associates often encounter challenges such as balancing sponsor requirements with site preferences, addressing complex regulatory and compliance issues, and ensuring contract language aligns with both parties' expectations. Negotiations may be prolonged due to differences in legal terms, indemnification, or budget concerns. Effective communication, attention to detail, and the ability to prioritize multiple agreements simultaneously are essential for overcoming these obstacles and maintaining positive relationships with sites.

What are the key skills and qualifications needed to thrive as a clinical contracts associate, and why are they important?

A Clinical Contracts Associate should possess strong knowledge of contract law, clinical trial processes, and regulatory compliance, typically supported by a bachelor's degree in life sciences, business, or a related field. Familiarity with contract management systems, Microsoft Office Suite, and eClinical tools is commonly required, and certifications such as CCRA or similar are advantageous. Excellent negotiation, attention to detail, and effective communication skills help manage stakeholder expectations and resolve issues efficiently. These skills are crucial for ensuring timely, compliant contract execution and supporting the smooth operation of clinical research projects.

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

AspectClinical Contracts Associate
Primary RoleDrafting, reviewing, and negotiating clinical trial contracts and budgets
Required SkillsLegal knowledge, contract management, attention to detail
Work EnvironmentCorporate or sponsor offices, legal or contracts departments
Common CertificationsNone specifically required, but legal or contract management certifications are a plus

The Clinical Contracts Associate primarily focuses on managing and negotiating contracts related to clinical trials, ensuring compliance and proper budgeting. In contrast, a Clinical Research Coordinator handles the day-to-day operations of clinical trials, including patient recruitment and data collection. Both roles are essential in the clinical research industry but serve different functions within the trial process.

What cities are hiring for Clinical Contracts Associate jobs?

Cities with the most Clinical Contracts Associate job openings:

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 Associate jobs?

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

Clinical Contracts Associate jobs near you

Clinical Contracts Associate

Fladger Associates

San Mateo, CA

Full-time

Posted 25 days ago

Job description

Foster City, CA
Contract Duration: 6-36 months
Rate: Negotiable
Salary: NA $1.00
Responsibilities:

  • Excellent employment opportunity for a Clinical Contracts Associate in the Foster City, CA.
  • Provide contract and payment administration support
  • Responsible for clinical administrative operations activities involving clinical finance support and/or assistance with contract negotiations.
  • Identifies issues/problems and provides customary recommendations for solutions.
  • May focus on either contracts or finance or both areas based on business need.
  • Coordinates and ensures that monthly payment processes are completed accurately and on time.
  • Works on diverse business problems that require financial analysis with oversight from more senior individuals in department.
  • Assists clinical teams in resolving financial issues as they relate to either site or vendor contracts.
  • Coordinates the preparation, execution, and tracking of domestic and/or international clinical site agreements, including study-specific budget templates, contracts and other documents with specific guidance from manager.
  • Works closely with internal and vendor clinical teams to ensure rapid start-up of study sites.
  • Responsible for tracking the progress of study-start-up activities as it relates to contracts and budgets.
  • Assists clinical teams in evaluating the progress of vendor contracts as the clinical program progresses.
  • Invoice review, expense account coding, and review routing.
  • Requires strong attention to detail, a high level of organization, and experience and aptitude to understand and utilize accounting systems.
  • Payment reconciliation: ability to research and review site payment data and determine payment status, determine if over or under payment has occurred, and answer site and team queries.
  • Requires in-depth and often complex investigation of payment discrepancies and thorough, yet efficient communication
  • Investigator Payment Generation: requires mastery of propriety clinical tracking system and ability to review and understand payment schedules and terms enter data and generate site payments on determined cycles.
  • Project management: ability to manage and lead projects cross-functionally from inception to completion.
  • Exercise knowledge in strategizing for the most effective methods, approaches, and level of communication and engagement.
  • Provide world-class customer service with internal and external customers.
  • Ability to maintain professionalism at all times especially during difficult interactions or items requiring escalation to senior management.
Experience:
  • Minimum 3-5 years of experience with a BA or BS in a relevant discipline.
  • Relevant experience typically includes contract administration or finance.
  • Pharma or Biotech experience preferred.
  • Demonstrates excellent verbal, written, and interpersonal communication skills.
  • Performs routine work without detailed instructions.
  • Demonstrates moderate proficiency in the use of complex budgeting & forecasting database tools.
  • Interacts well with clinical teams, legal, and corporate finance.
  • Performs routine work under moderate supervision and complex tasks under general supervision.
  • Consistently demonstrates the ability to understand and take effective approaches to varying levels of communication that would be most efficient and productive.

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