← Back to all open roles

Temp Corporate Contracts Manager II (Clinical Trial Contracts) - Alameda, CA (Updated to FULLY REMOTE)

Remote, CA6 MonthsLegalLife Sciences

Posted October 6, 2026 · ID 26065

Orbis Clinical is seeking a Temporary Corporate Contracts Manager II located in Alameda, CA (Fully remote or Fully onsite preferred or Hybrid 3x onsite week) for 6 months.


Job Title: Temporary Corporate Contracts Manager II

Location: Alameda, CA (Fully REMOTE or Fully onsite preferred or Hybrid 3x onsite week)

Contract: 6 months

Shift: 9am-5pm


Summary/Job Purpose:

The Temporary Corporate Contracts Manager II is responsible for drafting, negotiating and managing a variety of contracts supporting company's research, development, and supply chain functions, providing key support to advance company's 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


Top Skills:  

  • Direct experience drafting, redlining, and negotiating Clinical Study Agreements (CSAs), Clinical Trial Agreements (CTAs), and other clinical-study-related contracts. Candidate must have hands-on negotiation experience with counterparties, not just contract administration or coordination. 
  • Bachelor's degree and 2-3+ years of in-house contracts experience supporting contract drafting and negotiation within biotechnology, pharmaceutical, clinical research, or similar environments. 5+ years of relevant experience preferred. 
  • Broader experience supporting other areas of R&D contracting activities. 
  • Strong organizational and time management skills. 
  • Experience using a Contract Management system (Agiloft experience a plus; any CLM experience accepted). 


Strong Plus: 

  • Experience collaborating with and managing external vendors. 
  • Experience supporting vendor-related contracting activities, including negotiation of vendor agreements and collaboration with external service providers. 


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).


Compensation Details:

  • Orbis Clinical is an equal opportunity employer that provides a reasonable range of compensation for our positions. Actual compensation is influenced by a wide array of factors including, but not limited to, skill set, level of experience and specific office location.
  • The Pay Range for this position is $52.18 - $55.77 per hour, can vary depending on employment status.
  • Orbis Clinical offers eligible employees health benefits (medical, dental, and vision), employer-paid basic life and AD&D insurance, and a partial employer match on a 401(k). 


EEO and Reasonable Accommodation Statement:

Stone Harbor Staffing Group is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, genetic information, veteran status, or any other characteristic protected by law. We also consider qualified applicants with criminal histories, consistent with applicable law. If you need assistance or an accommodation during the application process, please contact us.


By applying for this position, you agree that any calls from Orbis Clinical and its subsidiaries may be monitored or recorded for training and quality assurance purposes.