McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve - we care.
What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow's health today, we want to hear from you.
Title: Staff Counsel - SCRI
Location: Nashville, Tennessee (Preferred)
Other locations: Atlanta, Georgia; Columbus, Ohio; Dallas, Texas; Richmond, Virginia
Hybrid or Remote
Required experience: 1-3 years healthcare experience
Description
In June 2022, McKesson and HCA Healthcare announced the creation of a joint venture that combined McKesson's US Oncology Research (USOR) and HCA Healthcare's Sarah Cannon Research Institute (SCRI). This joint venture established a fully integrated oncology research organization aimed at expanding clinical research, accelerating drug development and increasing availability and access to clinical trials for community oncology providers and patients, including those in underserved communities. In addition, through the combination of their clinical research networks, data and analytic capabilities and more, the joint venture brings greater efficiency to the drug development process - making it possible to help more cancer patients access new, life-saving medications.
Position Description
McKesson's Law Department is seeking an experienced healthcare and transactional lawyer to join the SCRI legal team and provide comprehensive legal support to its businesses. As Staff Counsel, you will serve as the initial point of contact on legal matters and provide day-to-day counseling on issues related to clinical trials, drug development, regulatory compliance, and other legal aspects specific to the oncology field. You will collaborate closely with internal stakeholders, including management, research teams, and business development, to ensure compliance with applicable laws, regulations, and industry standards.
The Staff Counsel responsibilities include the following:
- Staying current on relevant laws, regulations, and industry guidelines related to clinical trials, drug research & development, human research protection and data privacy & security.
- Overseeing and providing project management leadership to ensure successful implementation of legal guidance.
- Working independently and escalate issues to supervising attorneys as necessary.
- Drafting, reviewing and negotiating complex contracts, including clinical trial agreements, research services agreements, master services agreements, physician consulting agreements, confidentiality agreements, technology agreements, data use agreements and vendor contracts.
- Preparing legal presentations and memoranda for the senior attorneys and presenting to senior business unit leaders, as applicable
- Preparing contract summaries and/or issues lists to present to supervising attorney or business unit partners for review, if applicable.
- Recommending and implementing contracting policies, procedures and processes
- Coordinating with colleagues to identify regulatory issues, assess business impact risk and communicate same to business partners
- Working under supervision of supervising attorneys and exercising independent judgment in escalating issues within broadly defined practices and policies.
Qualifications
Minimum Requirements
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