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Clinical Trial Attorney Jobs (NOW HIRING)

Serve as a dedicated attorney supporting HVTI, with a primary focus on reviewing research agreements and clinical trial agreements. * Responsible for reviewing a high volume of contracts ...

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Kelley | Uustal trial attorneys have dramatically improved the lives of clients they represent. Our ... At least five (5) years of experience in clinical practice. Experience in a law firm/ legal ...

Kelley | Uustal trial attorneys have dramatically improved the lives of clients they represent. Our ... At least five (5) years of experience in clinical practice. Experience in a law firm/ legal ...

Kelley | Uustal trial attorneys have dramatically improved the lives of clients they represent. Our ... At least five (5) years of experience in clinical practice. Experience in a law firm/ legal ...

Kelley | Uustal trial attorneys have dramatically improved the lives of clients they represent. Our ... At least five (5) years of experience in clinical practice. Experience in a law firm/ legal ...

Kelley | Uustal trial attorneys have dramatically improved the lives of clients they represent. Our ... At least five (5) years of experience in clinical practice. Experience in a law firm/ legal ...

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Clinical Trial Attorney information

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$17

$39

$70

How much do clinical trial attorney jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for clinical trial attorney in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What are some common challenges faced by clinical trial attorneys in their daily work?

Clinical Trial Attorneys often navigate complex regulatory frameworks and tight timelines to review and negotiate contracts, which can be challenging given the high stakes of clinical research. They regularly balance the interests of sponsors, research sites, and regulatory bodies to ensure compliance and manage risk. Additionally, they stay current with evolving international, federal, and state laws impacting clinical trials. This role often involves close collaboration with cross-functional teams such as clinical operations, compliance, and research staff, making strong interpersonal skills and adaptability essential to resolving issues efficiently.

What is a clinical trial attorney?

A Clinical Trial Attorney is a legal professional who specializes in the regulatory, ethical, and contractual aspects of clinical research and drug development. They ensure that clinical trials comply with FDA regulations, ethical guidelines, and contractual obligations. Their responsibilities may include drafting and negotiating clinical trial agreements, advising on regulatory compliance, handling disputes, and mitigating legal risks for pharmaceutical companies, research institutions, or healthcare organizations. They play a crucial role in protecting patient rights while facilitating medical advancements.

What are the key skills and qualifications needed to thrive as a clinical trial attorney?

A Clinical Trial Attorney typically needs a law degree, active bar admission, and specialized expertise in clinical trial regulations, contracts, and compliance. Familiarity with regulatory databases, contract management software, and certifications such as CIPP/US (Certified Information Privacy Professional) are highly advantageous. Strong negotiation, analytical thinking, and communication skills enable success in collaborating with stakeholders and managing complex legal issues. These competencies are critical for ensuring clinical trials are conducted lawfully, ethically, and with minimal risk to sponsors and research sites.

More about Clinical Trial Attorney jobs
What cities are hiring for Clinical Trial Attorney jobs? Cities with the most Clinical Trial Attorney job openings:
What states have the most Clinical Trial Attorney jobs? States with the most job openings for Clinical Trial Attorney jobs include:
Infographic showing various Clinical Trial Attorney job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Associate Director, Legal Contracts

Travere

San Diego, CA

Full-time

Medical, Life, Retirement, PTO

Posted 23 days ago


Job description

Department:

101400 Legal

Location:

San Diego

Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease.

At Travere Therapeutics, we recognize that our exceptional employees are vital to our success. We are a dedicated team focused on meeting the unique needs of rare patients.Our work is rewarding - both professionally and personally - because we are making a difference. We are passionate about what we do.

We are seeking talented individuals who will thrive in our collaborative, diverse, fast-paced environment and share in our mission - to identify, develop and deliver life-changing therapies to people living with rare disease. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community.

At Travere Therapeutics, we are in rare for life. We continue to courageously forge new paths as we move toward a common goal of elevating science and service for rare patients.

Position Summary:

The Associate Director, Corporate Counsel, Legal Contracts is responsible for providing a high quality and diverse range of contractual legal services, while exercising discretion, professionalism, and solid judgment. In addition, the Associate Director, Corporate Counsel, Legal Contracts will draft and negotiate agreements, protecting the company's interests while ensuring the company's contractual arrangements are in compliance with applicable laws, as well as oversee and optimize contracts related policies and procedures.

Responsibilities:

  • Draft, review and negotiate a wide variety of agreements across many company departments including: Research and Development oriented agreements, Clinical Trial Agreements, Sponsored Research Agreements, Material Transfer Agreements, Licensing Agreements, Manufacturing Agreements, Master Services Agreements, Vendor Agreements, Consulting Agreements, Confidentiality Agreements, Operations oriented agreements, and Commercial oriented agreements. Draft and negotiate other types of agreements as needed.

  • Provide legal advice to the business on contract matters, including structuring, contract interpretation, compliance and enforcement, risk assessment, and legal and regulatory compliance.

  • Resolve legal and compliance issues using negotiation skills and expertise; negotiate with sophisticated counterparties.

  • Partner closely with the business to address current needs, anticipated future needs, and resolve internal and external business challenges and/or regulatory issues.

  • Assist with the optimization, implementation, and monitoring of contracting policies, procedures and programs, working closely with and partnering with the business and G&A functions.

  • Maintain a current working knowledge of new laws, case law trends with respect to contracts, regulatory developments, ; recommend process, product, or service improvements.

Education/Experience Requirements:

  • Juris Doctor (J.D.) from ABA accredited law school and active licensee of the California Bar in good standing or qualified to practice law as in-house counsel in California.

  • Minimum of 6 - 8 years of attorney experience, with combined corporate legal experience at a biotechnology, pharmaceutical, medical device or other life sciences company, and law firm preferred.

Additional Skills/Experience/Requirements:

  • The ideal candidate will embody Travere's core values: Courage, Community Spirit, Patient Focus and Teamwork.

  • Experience drafting and negotiating a broad range of contracts with experience specific to the life sciences industry (Collaboration Agreements, Sponsored Research Agreements, Clinical Trial Agreements, Master Service Agreements, License Agreements, Supply Agreements, Confidentiality Agreements, etc.)

  • Strong contract drafting and negotiation skills.

  • Excellent verbal and written communication skills, including the ability to succinctly explain reasons and purpose of contractual language as needed.

  • Experience using contract management systems.

  • Skilled at garnering cross-functional support with sensitivity and tact, embodying a collaborative mindset that puts the company first.

  • Strong attention to detail, the ability to see the big picture and recognize cross-functional effects.

  • Independent, self-starting individual with a demonstrated ability to thrive and prioritize work in a fast-paced environment.

  • Strong internal and external customer service mentality and sense of urgency.

  • Ability to work independently and contribute as part of a team.

  • Successful record of creating and managing complex project plans.

  • Ability to adapt to modification and changes to project plans, demonstrating flexibility to implement new strategies and tactics to accommodate these changes.

  • All positions have an essential job function to be able to perform face to face work with colleagues and/or onsite in San Diego. No role is expected to be 100% remote.

Total Rewards Offerings:
Travere provides comprehensive total rewards offerings that demonstrate our commitment as a diverse, equitable, people-centric, and pay-for-performance organization.

Benefits: Our benefits include premium health, financial, work-life and well-being offerings for eligible employees and dependents, wellness and employee support programs, life insurance, disability, retirement plans with employer match and generous paid time off.

Compensation: Our competitive compensation package includes a combination of both cash compensation (base pay and short-term incentive) and long-term incentive compensation (company stock), designed to recognize, retain, and reward employees.

Target Base Pay Range:

$173,000.00 - $225,000.00

*This information is current as of the date of this posting and may be modified in the future. Actual pay offered to a candidate will depend on a variety of factors including the candidate's experience, education, skills, and location.

Travere will accept applications on an ongoing basis until a candidate is selected for the position.

Travere Therapeutics, Inc. is an EEO/AA/Veteran/Disability Employer.

If you require a reasonable accommodation to complete the application or interview process, please contact us by sending an email to accommodations@travere.com. Please note that this email address is to be used exclusively to request an accommodation with the online application, interview or hiring process only. Travere HR will not reply to emails sent to this address for any other reason.