Senior Contracts Specialist- Biotech/Pharma/Medical Device ( Remote)

Location: Remote (U.S.)

Pay Rate: $55-$65hr ( Based on experience level)

Schedule: Full-Time | Monday-Friday

Duration: 8-9 Month Contract (Maternity Leave Coverage with Potential to Extend)

Our client recognizes that their exceptional employees are vital to their success. Their work is rewarding – both professionally and personally – because they are making a difference. The team is seeking talented individuals who will thrive in their collaborative, diverse, fast-paced environment and share in their mission – to identify, develop and deliver life-changing therapies to people living with rare disease. They are pursuing of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community. Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease!

About the Role

We are seeking an experienced Senior Contracts Specialist to support a fast-paced Research & Development (R&D) organization by managing the full contract lifecycle for a high volume of vendor and service agreements. This role is heavily focused on contract processing, documentation, and coordination, with much of the day spent reviewing, entering, tracking, and managing contracts through multiple systems.

The ideal candidate has experience within the biotechnology, pharmaceutical, life sciences, or medical device industry and is comfortable working cross-functionally with Clinical Operations, Regulatory, Legal, Procurement, and external vendors. This position requires exceptional attention to detail, patience, strong organizational skills, and the ability to manage multiple priorities while ensuring contracts move efficiently through the review and approval process.

Key Responsibilities

• Manage the full contract lifecycle, from contract request through execution, amendments, renewals, and contract closeout.
• Draft, review, and finalize a wide variety of contracts using approved company templates.
• Process and manage high-volume contract data entry, ensuring contract information is entered accurately and efficiently throughout the day.
• Maintain accurate contract records and supporting documentation within the Contract Lifecycle Management (CLM) system.
• Submit contract requests using Smartsheet (or similar tools), upload documentation into Coupa, and route agreements through Agiloft (or similar CLM system) for Legal review and approval.
• Track contracts throughout the approval process while ensuring all required documentation is complete.
• Partner closely with Clinical Operations, Research & Development (R&D), Regulatory Affairs, Legal, Procurement, Finance, Purchasing, and external vendors to ensure contracts move through the workflow efficiently.
• Review contract language for completeness, accuracy, consistency, and compliance with company policies.
• Monitor contract status and proactively follow up with internal stakeholders to prevent delays.
• Maintain detailed contract files, approval records, audit documentation, and supporting files.
• Support vendor onboarding and supplier contract activities.
• Assist with developing and improving contract templates, SOPs, workflows, and contract management processes.
• Communicate contract processes and requirements to internal business partners who may not be familiar with contracting procedures.
• Support multiple projects simultaneously while meeting deadlines in a collaborative, fast-paced environment.

Required Qualifications

• 4-10 years of experience as a Contract Specialist, Contract Administrator, or similar contracts-focused role.
• Must have experience within the biotechnology, pharmaceutical, life sciences, or medical device industry.
• Experience managing the entire contract lifecycle, including drafting, reviewing, processing, executing, renewing, and amending contracts.
• Hands-on experience using Contract Lifecycle Management (CLM) systems to manage and track contracts.
• Experience using Agiloft (Preferred) or a similar CLM platform.
• Experience using Coupa for procurement and contract workflows.
• Experience maintaining accurate contract records and supporting documentation within a CLM system.
• Experience using Smartsheet (preferred), Google Sheets, and/or Microsoft Excel to manage contract requests and workflow tracking.
• Understanding of submitting contract requests through workflow tools (such as Smartsheet), uploading documentation into Coupa, and routing contracts through Agiloft (or similar platform) for Legal review.
• Experience spending the majority of the workday processing, reviewing, entering contracts.
• Strong experience drafting, reviewing, and finalizing contracts using approved company templates.
• Experience with: Master Service Agreements (MSAs) Consulting Agreements, Service Agreements, Confidentiality Agreements (NDAs/CDAs),Statements of Work (SOWs).Work Orders. Change Orders , Amendments
• Experience working closely with Clinical Operations, Research & Development (R&D), Regulatory Affairs, Legal, Procurement, and vendor management teams.
• Experience with vendor onboarding, supplier contract management, and procurement workflows.
• Highly collaborative with excellent verbal and written communication skills.
• Patient, flexible, and comfortable explaining contract processes to internal stakeholders who may not be familiar with contracting procedures.
• Experience working in a remote setting – reliable internet and home office
• Bonus: Experience developing or improving contract templates, SOPs, workflows, and business processes
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What We're Looking For

• Highly organized with exceptional attention to detail.
• Collaborative team player who enjoys partnering with Legal, Clinical, Procurement, and business teams.
• Comfortable spending much of the day reviewing, entering, and managing contracts.
• Able to communicate contract processes clearly to both technical and non-technical stakeholders.
• Thrives in a fast-paced environment while maintaining accuracy and quality.
• Self-motivated, dependable, and able to manage multiple priorities independently.

TCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.