Global Regulatory Counsel

At LabCorp, you are part of a journey to accelerate life-changing healthcare breakthroughs and improve the delivery of care for all. You'll be inspired to discover more, develop new skills and pursue career-building opportunities as we help solve some of today's biggest health challenges around the world. Together, let's embrace possibilities and change lives!LabCorp is searching for a Global Regulatory Compliance Attorney as a member of the LabCorp Corporate Compliance Department. This Department is committed to a trusting and collaborative culture where we value growth and development. We engage proactively with our business colleagues in maintaining the company's commitment to a strong culture of compliance.The successful candidate will:Possess working knowledge of regulatory, compliance, and other legal issues related clinical laboratories, in vitro diagnostic devices, clinical trials, and global trade, including: (1) FCPA and other anti-bribery regulations; (2) importexport compliance; (3) global trade regulations (4) FDA regulations (and other international equivalents); (5) ICH-GxP requirements; and (6) global medical device and in vitro diagnostic registration requirementsProvide day-to-day compliance and regulatory counselingConduct foreign third-party due diligence, including post-contract monitoring, risk evaluations and reviewImplement and oversee compliance policy and training updatesProvide legal support in responding to government and client audits or investigationsMonitor and analyze legal and regulatory changesParticipate in acquisition due diligence and integration of compliance programUnderstand and be able to clearly articulate to the business the legal ramifications of varied regulatory issues, succinctly articulate risks, and offer potential solutionsBe a "hands-on" attorney who is able to effectively collaborate across the organizationEducationQualificationsRequirementsLicenseCertificationEducation: A Juris Doctor (JD) degree from an ABA-accredited law school is required. Education and Experience: JD from ABA accredited law schoolMinimum of 1-3 years of overall experience (law firm or in-house)Admission to a US State BarAnti-bribery regulations, global trade regulations, and FDAmedical device regulations experienced highly preferredSolid working knowledge of laws, regulations, and industry standards (e.g. ISO 13485) that affect the development and commercialization of pharmaceutical and biotechnology products and impact a global organizationTeam player with excellent judgment and interpersonalcommunication skillsAbility to constructively counsel and influence clients in making the right decisionsCapacity to simultaneously handle a variety of complex legal matters with minimal guidanceDemonstrable experience taking ownership of issues and providing practical adviceAbility to prioritize and undertake mission critical tasks in a fast-paced environmentExperience in the global healthcare industryApplication Window: 10202024Hours 8am EST to 5pm ESTBenefits: All job offers will be based on a candidate's skills and prior relevant experience, applicable degreescertifications, as well as internal equity and market data. Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STDLTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Commissions, and Company bonus where applicable. For more detailed information, please click here.

Created: 2024-11-02