Clinical Trials Partner

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July 30

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Briefly™️

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SaaS • B2B • Marketplace

Briefly is a comprehensive platform designed to assist freelancers, agencies, and service providers in securing and managing clients more effectively. It provides tools for business growth, client management, accounting, invoicing, and more from a single dashboard. With over 1800 vendors in its base, Briefly facilitates perfect matchmaking between clients and service providers, ensuring detailed scope of work and seamless interaction through text, calls, and video chat. The platform automates business development processes, providing transparency and efficiency in client engagements, from initial introduction calls to pitch submissions and beyond. Briefly aims to simplify the client's acquisition and management process while ensuring timely payments and accurate work scopes, making it an essential tool for anyone offering brand building services.

11 - 50 employees

☁️ SaaS

🤝 B2B

🏪 Marketplace

📋 Description

• WHO WE ARE.... • Outside GC, the nation’s leading partner-only provider of on-demand general counsel services, is a thriving and expanding virtual law firm offering an innovative approach to legal services for early-stage, growing, and mature businesses. With a team of senior business lawyers with substantial in-house and general counsel experience, Outside GC provides private and public companies and non-profit organizations with outstanding corporate and IP legal services as needed at a fraction of the cost of either hiring a full-time general counsel or relying exclusively on law firm counsel. Clients typically develop a working relationship with one Outside GC lawyer and have access to the whole team for specific subject-matter experience.

🎯 Requirements

• Experience: At least 10+ years of corporate legal practice, including experience as an in-house attorney, serving as a General Counsel and/or in another senior in-house legal role, and 3+ years of law firm training • Specialized Expertise: • Significant experience drafting and negotiating clinical trial agreements, contract research agreements, and sponsored research agreements for biotech, pharma, and academic research institutions • Proven track record supporting life sciences clients through all phases of clinical development, including vendor and manufacturing agreements, software and data licensing, and regulatory infrastructure • Deep understanding of multi-site research frameworks, including IRB reliance arrangements and compliance with NIH’s Single IRB Review Policy • Skilled in navigating complex regulatory environments involving human subject protections, research misconduct, and HIPAA compliance • Experience working with academic medical centers, hospitals, and federal research agencies to design and implement streamlined, scalable contracting and compliance protocols • Familiarity with secondary use of clinical trial data, data de-identification, and data sharing agreements (DSAs, DTAs) • Demonstrated success as a practical, business-focused, and responsive legal partner • J.D. from a nationally accredited law school • State bar membership in state where reside/practice

🏖️ Benefits

• Flexibility to work full-time, part-time, and during preferred times as part of a fully remote team • High-quality legal engagements • The collegiality and camaraderie of highly experienced and talented colleagues to share resources, referrals, and coverage • The support of an outstanding team of financial, operations, client relations and business development professionals to facilitate the delivery of exceptional, pragmatic, and cost-effective legal services to our clients