bluebird bio
Paralegal Contracts Specialist
This job is now closed
Job Description
- Req#: 7074875
Employer Industry: Biotechnology
Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Supportive and collaborative work environment
- Engage in meaningful work that contributes to innovative gene therapies
- Chance to work with diverse teams and integrate multiple viewpoints
- Competitive pay and comprehensive benefits package
What to Expect (Job Responsibilities):
- Draft, review, and negotiate a high volume of routine legal agreements, including Confidentiality Agreements, Material Transfer Agreements, Consulting Agreements, Sponsored Research Agreements, Master Services Agreements, and Work Orders
- Support legal and scientific teams in executing agreements with CROs, academic collaborators, vendors, and consultants
- Maintain and organize the contract management system while ensuring accurate document tracking and version control
- Collaborate with stakeholders across R&D, finance, and business development to ensure contracts meet operational needs and compliance standards
- Monitor contract terms and timelines, including renewals, expirations, and obligations
What is Required (Qualifications):
- Bachelor's degree required; Paralegal certification preferred
- Minimum of 3–5 years of relevant experience, preferably in a biotech, pharmaceutical, or life sciences setting
- Familiarity with pre-clinical research operations and regulatory environment (e.g., IACUC, IRB, GLP)
- Experience with contract lifecycle management (CLM) systems and document management tools
- Exceptional organizational and communication skills, with strong attention to detail
How to Stand Out (Preferred Qualifications):
- Experience in drafting and negotiating contracts within the biotech or pharmaceutical industry
- Familiarity with FDA, NIH, and GLP standards
- Ability to thrive in a fast-paced, collaborative environment
#Biotechnology #ContractsSpecialist #CareerOpportunity #CollaborativeWorkEnvironment #GeneTherapies
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We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer.About the company
bluebird bio, Inc., The company's only - in the European Union - approved drug is betibeglogene autotemcel, which treats transfusion-dependent beta thalassemia, a rare genetic blood disorder, and has been approved for use by the European Medicines Agency.
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