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Corporate Paralegal

Job in South San Francisco, San Mateo County, California, 94083, USA
Listing for: ALTEN
Full Time position
Listed on 2026-01-12
Job specializations:
  • Law/Legal
    Regulatory Compliance Specialist, Business Law
  • Business
    Regulatory Compliance Specialist, Business Law
Salary/Wage Range or Industry Benchmark: 60000 USD Yearly USD 60000.00 YEAR
Job Description & How to Apply Below

Position: Full-time with minimum 2 days onsite (Mondays and Wednesdays) in South San Francisco.

Contracts Management
  • Draft, review, and edit routine contracts (e.g., NDAs, service agreements, consulting agreements, supply and vendor contracts, master service agreements and associated work orders, material transfer agreements, and clinical trial agreements).
  • Manage the contract lifecycle, including intake, tracking, execution, and archiving through contract management systems/database.
  • Support counsel and internal clients with redlines, revisions, and communication with counter parties.
  • Monitor contract compliance and key obligations, and coordinate renewals or amendments.
  • Assist with continued development and revision of standard form agreements.
Corporate Governance & Entity Management
  • Maintain corporate records, including minutes, resolutions, bylaws, and organizational documents.
  • Coordinate annual filings, business licenses, and other regulatory filings as required.
  • Assist in preparing board and committee materials and maintaining governance calendars.
  • Support compliance initiatives and corporate policies (e.g., signature authority, document retention).
General Legal Support
  • Assist with due diligence, audits, and internal or external inquiries.
  • Support implementation and internal training of contract forms and procedures and legal/compliance SOPs.
  • Manage Legal Department's internal intranet page and employee-accessible SharePoint files.
Skills
  • Strong understanding of corporate governance principles.
  • Knowledge and understanding of global regulations and guidelines, including those related to GxP.
  • Ability to regularly communicate highly confidential information to senior level staff.
  • Ideal candidate is flexible and willing to learn new procedures and skill sets.
  • Must be able to collaborate and work with other departments such as Clinical, Commercial, Finance, Research & Development, Manufacturing, and Supply Chain/Purchasing.
  • Ability to work in a fast‑paced, deadline‑driven environment.
  • Strong attention to detail and ability to multitask and handle multiple contract negotiations simultaneously.
  • Excellent organizational skills and ability to prioritize effectively to deliver results within reasonable timelines.
  • Proficient in MS Word, Excel, PowerPoint, Outlook, SharePoint, and related software.
  • Ability to work independently and as part of a team.
  • Strong interpersonal skills, including verbal and written communication.
Education & Experience
  • Bachelor's degree required; paralegal certificate from an accredited program preferred.
  • Minimum 5 to 10 years of contracts and/or corporate experience, preferably in a biotech or pharma company.
  • Experience with reviewing confidentiality agreements, master service agreements, material transfer agreements and associated work orders, supply chain agreements, and clinical trial agreements.
  • Candidates must be authorized to work in the U.S.
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