Overview
This role is responsible for drafting, negotiating, and managing a variety of contracts that support research, development, and supply chain functions.
Responsibilities
- Draft, negotiate, and manage a wide range of contracts under close supervision, which may include:
- Confidentiality agreements
- Consulting and service agreements
- Materials transfer agreements
- Research agreements
- Clinical study agreements
- Vendor services agreements
- Advise and troubleshoot on existing agreements under supervision.
- Define and communicate contract-related risks to appropriate internal decision-makers for discussion and resolution.
- Interact with internal stakeholders to address legal and business questions.
- Handle miscellaneous legal tasks on an as-needed basis under supervision.
- Maintain and track contracts status.
- Provide support to in-house attorneys as requested.
- Perform other duties as assigned.
- Comply with all policies and standards.
Requirements
Education and Experience
- BS/BA degree in a related discipline and 7 years of related experience; or
- JD preferred; or
- Equivalent combination of education and experience.
Experience (required)
- Bachelor’s degree and 2–3 years of in-house experience at a biotechnology, pharmaceutical, or high-tech company, with a focus on contract drafting and negotiation.
Knowledge, Skills, and Abilities (required)
- Thorough understanding of the contract management process, including tracking, negotiation, approval, and signature processes.
- Ability to work independently and effectively across functional groups (e.g., Commercial, Research and Development, CMC, Human Resources, Finance, Facilities, IT, and Investor Relations) and all levels of management.
- Flexibility and willingness to learn new procedures and skill sets.
- Detail-oriented with strong organizational skills.
- Ability to handle multiple tasks simultaneously.
- Ability to prioritize; responsible and conscientious.
- Ability to work under pressure to meet specific deadlines.
- Commitment to quality and reliability in all work tasks.
Preferred Qualifications
- Working knowledge of the drug discovery and development process, including the ability to understand risks and requirements associated with pharmaceutical contracting.
- Experience with or knowledge of paralegal support tasks, with a focus on intellectual property matters or corporate matters.
- Clear and concise verbal and written communication skills, with excellent interpersonal communication.
- Strong computer skills (e.g., Microsoft Word, Excel, and PowerPoint).
Compensation & Benefits
- Base pay range: $122,000 - $173,000 annually.
- Base pay may be adjusted based on geographic region tied to defined U.S. markets, as well as job-related knowledge, skills, experience, and internal equity.
Benefits (as part of Total Rewards):
- 401k plan with generous company contributions
- Group medical, dental, and vision coverage
- Life and disability insurance
- Flexible spending accounts
- Discretionary annual bonus program (or, if field sales staff, a sales-based incentive plan)
- Opportunity to purchase company stock and receive long-term incentives
- 15 accrued vacation days in the first year
- 17 paid holidays including a company-wide winter shutdown in December
- Up to 10 sick days throughout the calendar year
Location and Travel
- Travel requirement: 0% (no travel required).
Working Conditions
- Modern office environment designed to support collaboration.
- Company-provided equipment, including dual monitors and ergonomic chairs.
Equal Opportunity
- Equal Opportunity Employer. No discrimination based on race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, disability, or other protected class status under applicable federal, state, or local law.
Disclaimer
This job description is intended to describe the general nature and level of work performed and is not a complete inventory of all duties, responsibilities, and qualifications required for the role.