Senior Patent Attorney supporting pharmaceutical product discovery and development at Lilly. Collaborating with scientists and legal teams to manage complex IP strategy.
About the role
- Senior Counsel providing legal guidance for data generation and scientific communications at GSK. Supporting legal compliance and strategic initiatives while collaborating with Medical Affairs and regulatory teams.
Responsibilities
- Provide legal advice and support on data generation activities, including clinical trials, real-world evidence, and observational studies
- Counsel on scientific communications to HCPs, Regulators, Payers, Patient Advocacy Groups, etc, through various in-person and digital channels such as Congress settings, medical education, Medical Information inquiries, etc
- Advise on regulatory and compliance matters related to medical and scientific activities, ensuring alignment with applicable laws and GSK policies
- Draft, review, and negotiate agreements related to data generation and scientific communications, such as research collaborations and service agreements
- Collaborate with cross-functional teams, including Medical Affairs, CMO Office, Commercial, Compliance, and Regulatory, to address legal risks and support strategic initiatives
- Manage external legal counsel to ensure high-quality, cost-effective legal services
Requirements
- Qualified solicitor or barrister in the UK with a current practicing certificate OR US qualified lawyer
- A demonstrable number of years of legal experience, including advising on regulatory, compliance, and commercial matters
- Strong knowledge of laws and regulations related to data generation, scientific communications, and healthcare interactions
- Proven ability to provide clear, pragmatic legal advice in a fast-paced environment
- Experience drafting and negotiating complex agreements
- Excellent interpersonal and communication skills, with the ability to build trusted relationships across teams
- In-house legal experience within the pharmaceutical or healthcare industry (preferred)
- Familiarity with global regulatory frameworks and compliance requirements (preferred)
- Experience advising on clinical trials, real-world evidence, or observational studies (preferred)
Benefits
- Health insurance
- Flexible working hours
- Professional development opportunities
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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