About this role
<p>B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap® and CAPS®.</p> <p>Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise® philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit <a href="http://www.bbraunusa.com">www.bbraunusa.com</a></p> <div> <h3> </h3> <h3><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><strong>Position Summary</strong></span></h3> <p><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">B. Braun is seeking a strategic and influential <strong>Senior Director, Medical Affairs</strong> to lead Clinical Trials and Pharmacovigilance across North America. This executive leader will drive clinical and safety strategy, ensure regulatory compliance, and partner with R&D, Regulatory, Commercial, and Global Medical Affairs teams to shape product development and lifecycle management. The ideal candidate combines deep scientific expertise with strong leadership, sound medical judgment, and the ability to thrive in a dynamic, global environment.</span></p> <p> </p> <h3><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><strong>Key Responsibilities</strong></span></h3> <ul> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Lead Clinical Trials and Pharmacovigilance teams across the U.S. and Canada.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Develop and execute clinical study plans and publication strategies for new and existing products.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Serve as the Local Safety Officer (LSO), providing oversight of adverse event assessments and regulatory reporting decisions.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and company policies.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Partner with global and cross-functional teams to drive clinical evidence generation and product strategy.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Provide medical and scientific leadership to support regulatory, commercial, and product development initiatives.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Mentor and develop leaders while fostering a high-performing, collaborative culture.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Manage departmental budgets, resources, and long-range strategic priorities.</span></li> </ul> <h3> </h3> <h3><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><strong>Qualifications</strong></span></h3> <ul> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">MD, PharmD, or PhD required.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">10–15 years of experience in Medical Affairs, Clinical Development, Pharmacovigilance, or related life sciences functions.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Minimum 5 years of leadership experience managing teams and leaders.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Experience with pre-market and post-market clinical evidence generation, preferably within medical devices or combination products.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Proven success leading in a matrixed, global organization.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Strong understanding of clinical research, regulatory requirements, and drug/device safety.</span></li> </ul> <h3> </h3> <h3><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><strong>Key Skills</strong></span></h3> <ul> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Strategic leadership and executive presence.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Expertise in clinical trials, pharmacovigilance, and regulatory compliance.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Exceptional communication and presentation skills.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Ability to influence cross-functional and global stakeholders.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Strong decision-making skills in complex, high-impact situations.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Ability to drive operational excellence and organizational change.</span></li> </ul> <h3> </h3> <h3><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><strong>Work Environment</strong></span></h3> <ul> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Hybrid role with a preference for candidates located in Pennsylvania; relocation assistance available.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Onsite presence required at least three days per week.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Up to 30% domestic travel.</span></li> <li style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Fast-paced, highly collaborative environment with significant interaction across global teams and senior leadership.</span></li> </ul> <p style="font-size:12.0pt"> </p> <p style="font-size:12.0pt"><span style="font-size:12.0pt;font-family:tahoma, arial, helvetica, sans-serif">Salary Range: $200,000-$300,000</span></p> <p style="font-size:12.0pt"> </p> </div><p>The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate.</p> <p>B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at <a href="http://www.bbraunusa.com">www.bbraunusa.com</a>.</p> <p>Through its “Sharing Expertise®” initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services.</p> <p><em>We are an equal opportunity employer. We evaluate applications without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected characteristic. Know Your Rights: Workplace Discrimination is Illegal, <a href="https://www.eeoc.gov/poster">click here</a>.</em></p>