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Contracts Specialist II

Role overview

Qualifications

  • Bachelor's Degree in Business, Legal Studies, Healthcare Administration, Life Sciences, or a related discipline
  • Minimum of 3 years of commercial contracting, legal operations, contract administration, or related experience
  • Knowledge of contract lifecycle management processes and contract best practices
  • Strong organizational skills with the ability to manage multiple priorities and deadlines

Responsibilities

  • Independently create, review, negotiate, and manage Confidential Disclosure Agreements (CDAs), Work Orders (WOs), and other agreements
  • Conduct independent legal review of Change Orders (COs) as required
  • Manage and track contract escalations to Subject Matter Experts (SMEs)
  • Maintain organized electronic document repositories for approvals, contract versions, and executed agreements

Key facts

Other skills

  • Organizational Skills
  • Communication
  • Problem Solving
  • Decision Making

About the company

Clario logo

Clario

Contract Research Organizations (CRO)

Clario is a leading healthcare research and technology company that generates high quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac safety, medical imaging, precision motion, and respiratory endpoints. Since our founding more than 50 years ago, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported clinical trials over 26,000 times in more than 100 countries. Our global team of science, technology, and operational experts have supported over 60% of all FDA drug approvals since 2019. For more information, visit Clario.com

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size1001 - 5000

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Job description

At Clario, a part of Thermo Fisher Scientific, our contracts team plays a critical role in accelerating clinical research by ensuring efficient, compliant, and commercially sound agreements with clients and partners worldwide. As a Contract Specialist II, you will independently manage a broad range of commercial contracting activities, support contract negotiations, and collaborate with internal stakeholders and external clients to facilitate timely contract execution. This role is ideal for a professional who thrives in a fast-paced environment and enjoys balancing legal, operational, and business priorities while supporting global clinical trial initiatives.

What We Offer

  • Competitive pay and incentives

  • Provident fund and medical insurance

  • Engaging employee programs and local events

  • Modern office spaces and remote work flexibility

What You'll Be Doing

  • Independently create, review, negotiate, and manage Confidential Disclosure Agreements (CDAs), Work Orders (WOs), Start-Up Agreements (SUAs), and Letters of Intent (LOIs) in accordance with Clario contracting standards.

  • Conduct independent legal review of Change Orders (COs) as required.

  • Independently create, review, and negotiate Master Service Agreements (MSAs), Quality Agreements (QAs), Service Level Agreements (SLAs), Stand-Alone Agreements (SAAs), and Data Processing Agreements (DPAs).

  • Manage and track contract escalations to Subject Matter Experts (SMEs) for terms outside approved standards or playbooks.

  • Review legal language and provide contract interpretation and guidance with appropriate senior oversight.

  • Update, manage, prioritize, and maintain assigned contract cases within Salesforce.

  • Accurately enter and maintain contractual data, legal terms, and supporting documents in Salesforce.

  • Support the monitoring and management of centralized team mailboxes and action requests.

  • Contribute to updates of Commercial Contracting Quick Reference Guides (QRGs) and process documentation.

  • Conduct peer reviews and provide support to more junior team members.

  • Maintain organized electronic document repositories for approvals, contract versions, and executed agreements.

  • Review, track, process, store, and communicate electronic signature activity in accordance with company standards.

  • Participate in departmental and cross-functional projects to support continuous improvement initiatives.

  • Support client, internal, and regulatory audits as assigned.

  • Ensure compliance with company SOPs, training requirements, and quality standards.

What We Look For

  • Bachelor's Degree in Business, Legal Studies, Healthcare Administration, Life Sciences, or a related discipline, or an equivalent combination of education and relevant experience.

  • Minimum of 3 years of commercial contracting, legal operations, contract administration, or related experience.

  • Experience reviewing and negotiating complex and non-standard commercial agreements.

  • Knowledge of contract lifecycle management processes and contract best practices.

  • Experience within pharmaceutical, healthcare, clinical research, Contract Research Organization (CRO), or life sciences environments preferred.

  • Proficiency with Microsoft Office applications, including intermediate Microsoft Word and Excel skills.

  • Experience working with Salesforce or similar contract management systems preferred.

  • Strong organizational skills with the ability to manage multiple priorities and deadlines.

  • Excellent verbal and written communication skills with strong client-facing abilities.

  • Exceptional attention to detail, judgment, and problem-solving capabilities.

  • Ability to work independently while contributing effectively within a collaborative team environment.

  • Ability to perform successfully in a fast-paced, metrics-driven environment requiring sound decision-making and adaptability.


At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to workβ€”and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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