Target PR Range: 43-53/hr DOE
SUMMARY/JOB PURPOSE
The Temporary Corporate Contracts Manager II is responsible for drafting, negotiating and managing a variety of contracts supporting research, development, and supply chain functions, providing key support to advance mission.
ESSENTIAL DUTIES/RESPONSIBILITIES
- Draft, negotiate and manage a wide range of contracts (which may include confidentiality agreements, consulting and service agreements, materials transfer agreements, research agreements, clinical study agreements, and various vendor services agreements) under close supervision.
- Advise and troubleshoot on existing agreements under supervision.
- Define risks related to contracts documents and relationships, and be able to communicate those risks to appropriate internal decision-makers for discussion and resolution.
- Interact with various internal clients effectively to address legal and business questions.
- Handle miscellaneous legal tasks on an as needed basis under supervision.
- Maintain and track status for contracts.
- Provide support to in-house attorneys as requested.
- Performs other duties as assigned
- Complies with all policies and standards
SUPERVISORY RESPONSIBILITIES
- No supervisory responsibilities
EDUCATION/EXPERIENCE/KNOWLEDGE/SKILLS & ABILITIES
Education
- BS/BA degree in related discipline and 7 years of related experience; or
- JD preferred; or
- Equivalent combination of education and experience.
Experience
- 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 both independently and effectively across a variety of functional groups (such as Commercial, Research and Development, CMC, Human Resources, Finance, Facilities, IT and Investor Relations) and all levels of management.
- Flexible and willing to learn new procedures and skill sets.
- Must be detail oriented and have strong organizational skills.
- Ability to handle multiple tasks simultaneously.
- Ability to prioritize; must be responsible and conscientious.
- Ability to work under pressure to meet specific deadlines.
- Dedication to quality and reliability in all work tasks.
Preferred:
- Working knowledge of the drug discovery and development process and ability to understand risks and requirements associated with pharmaceutical contracting preferred.
- Experience with or knowledge of paralegal support tasks, with a focus on intellectual property matters or corporate matters, preferred. Clear and concise verbal and written communication skills; must have excellent interpersonal communication skills. Strong computer skills (e.g., Microsoft Word, Excel and PowerPoint).