Biopharmaceutical Attorney (Part-Time)
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Biopharmaceutical Attorney (Part-Time)
Our Client - Pharma & Biotech company
- Remote
$200.00 - $250.00/hour
Exact compensation may vary based on skills, experience, and location.
20 hrs/wk
Contract (1099)
Remote work yes (100%)
Travel not required
Start date
October 19, 2026
End date
October 19, 2027
Superpower
Legal
Capabilities
Contracts & Document Review
Preferred skills
Clinical Research
Clinical Trials
Pharmaceuticals
Biotechnology
Informed Consent
Negotiation
Confidentiality
Data Privacy
Preferred industry experience
Pharma & Biotech
Experience level
5 - 8 years of experience
Job description
Core Responsibilities
- Review of clinical trial site confidentiality and non-disclosure agreements, clinical trial agreements and country-specific informed consent form templates
- Review and negotiate clinical trial site confidentiality and non-disclosure agreements, clinical trial agreements and informed consent forms across various global regions for Phase 3 clinical trials
- Collaborate with internal clinical operations, clinical development and regulatory teams and our external clinical research organization in the review of clinical trial related documents
- Review and negotiate confidentiality and non-disclosure agreements, master services agreements, consulting agreements and statements of work
- Initial and ongoing development of clause playbooks and negotiation parameters for clinical trial related contracts and vendor related contracts
Qualifications/Skills
- Minimum of 5-8 years of legal experience with public biotechnology or pharmaceutical companies
- Strong knowledge of laws and regulations relevant to the industry, including FDA law and regulations, GCP as adopted by the FDA and ICH, US Anti-Kickback Statute, and global Anti-Fraud statutes
- Deep understanding of applicable data privacy and data governance regulations both in the US and internationally
- Strong experience negotiating with universities and academic medical centers in the US and internationally
Benefits/Perks
- Fully remote
- No travel required
- Flexible hours
All applicants applying for U.S. job openings must be legally authorized to work in the United States and are required to have U.S. residency at the time of application.
If you are a person with a disability needing assistance with the application, or at any point in the hiring process, please contact us at support@themomproject.com.
Screening Questions
- Approximately how many Phase 2 and/or Phase 3 global clinical trials have you worked on for pharmaceutical companies in the last 5 years and what regions globally did they cover?
- Are you familiar with the various laws and regulations relevant to the industry as listed in the job description and are you comfortable answering questions from internal stakeholders as they related to clinical trials?
- What type of experience do you have with the review and negotiation of NDAs, MSAs, SOWs and other similar contracts in the pharmaceutical field?