VP, Clinical Trials – SHV & ICTx

Additional Location(s):US-MA-Marlborough Diversity – Innovation – Caring – Global Collaboration – Winning Spirit- High Performance At Boston Scientific, well give you the opportunity to harness all thats within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, well help you in advancing your skills and career. Here, youll be supported in progressing – whatever your ambitions. About the role: Boston Scientific is seeking a highly experienced and visionary Vice President, Clinical, Structural Heart Valves (SHV) and ICTx Clinical Operations to lead and drive the clinical research for SHV and Clinical Operations efforts of our ICTx Team. The successful candidate will be responsible for overseeing the design, execution, and interpretation of clinical trials, ensuring the safety, efficacy, and regulatory compliance of our products. This role will play a pivotal role in shaping the SHVs clinical strategy, working closely with cross-functional teams to advance the safe and efficacious utilization of our product portfolio. This role will report into the Chief Medical Officer ICTx and will sit on the ICTx leadership team. Your responsibilities will include: Clinical Strategy and Leadership: Provide strategic guidance and support to the core functions of the Clinical Sciences team, overseeing franchise Clinical Strategy, Clinical Operations, and Clinical Evidence. Ensure excellence in planning and execution of SHV clinical programs. Drive the collaborative development and execution of the SHV clinical development strategy – working in conjunction with the business to deliver in alignment with the company and divisions overall vision and objectives. Collaborate with executive leadership to align clinical objectives with the companys business strategy and key internal and external customers and stakeholders. Stay abreast of advancements in clinical science, therapeutic trends, and regulatory guidelines – providing medical expertise to the Division on forward-looking product development and clinical strategy. Drive innovation in all clinical science areas, including design, methods, data sources, partnerships, and other clinical engagement. Provide clinical input for the upstream development of new products, the continued improvement of existing products, and the assessment of potential acquisitions. Partner with the Chief Medical Officer to build and maintain relationships with external KOLs, academic institutions, and professional societies to enhance the organizations scientific credibility and reputation, and to provide meaningful insights into the Urology clinical research strategies. Support clinical diligence associated with business development, merger, and acquisition initiatives. Clinical Trial Design and Execution: Provide strategic guidance on the design and planning of clinical studies, ensuring robust protocols that meet regulatory requirements and generate meaningful data that will support the safe and efficacious adoption of products following launch. Provide leadership as needed on the conduct of clinical trials, ensuring compliance with GCP, relevant regulations, and ethical standards. Ensure clinical trial progress and effectiveness, resolving escalated challenges and potential risks. Drive effective and efficient clinical operations by continually strengthening the organizations strategic approach to evidence generation (e.g., Trial strategies) and trial execution (e.g., insource vs. outsource considerations). Clinical Evidence Evaluation: Oversee the development and implementation for Clinical Evaluation Plans, Reports, and Post-Market Clinical Evaluation Plans, and Reports. Collaborate with key stakeholders to identify communication priorities and target audiences. Providing clinical perspective and input to cross-functional teams such as risk management, product managemen , and post-market surveillance. People Leadership: Attract top talent and build a high-performing team to deliver on Divisions goals and objectives. Excel at clear and transparent communication, ensuring that information flows smoothly both top-down and bottom-up within the team. Actively listening to the teams concerns and ideas will be crucial in building a culture of trust and collaboration. Actively promote diversity and inclusion within the workplace. Value individual differences and foster an inclusive culture for a richer and more innovative work environment. Commitment to fostering professional growth and creating a supportive work environment that will empower individuals to reach their fullest potential. Set clear performance expectations and goals for team members. Track and evaluate performance, recognize achievements, and address challenges to drive continuous improvement. Culture: Foster a culture of scientific excellence, continuous learning, and appropriate risk-taking within the team. Ensure that Clinical Sciences excels in the areas of strategic thinking, accountability to business needs and goals, and acting as collaborative partners will all stakeholders and customers. Provide leadership and advocacy for organizational change strategies, including structural, cultural, and strategic change. Act as a change agent across areas of responsibility to drive the evolution of the Clinical Science organization forward and ensure change readiness and capability of organizations under leadership. Identify and drive continuous improvement activities across Clinical Science, and works to instill a culture of continuous improvement, transparency and problem-solving across the organization. Cross-functional Collaboration: Collaborating with internal teams, including R&D, Regulatory, Quality, Marketing, Commercial and Business Development, to integrate clinical insights into overall product development and commercialization strategies. Work closely with Regulatory Affairs leadership to ensure timely and successful submission of clinical trial applications and product registrations, including representing the company in interactions with regulatory authorities to gain approval for clinical trials and product marketing applications. Work closely with external partners, including contract research organizations (CROs), the Companys Global Commercial Operations group (GCO), academic institutions, and key opinion leaders to facilitate investigator-sponsored and collaborative clinical research efforts. Required qualifications: Advanced degree (Ph.D., MD, or equivalent) in a relevant scientific discipline preferred. Minimum 10 years of experience in clinical research and development within the healthcare or pharmaceutical industry, including leadership roles. Preferred qualifications: Proven track record of leading organizations through successful clinical trial design, execution, and regulatory submissions. Strong knowledge of clinical trial regulations, GCP guidelines, and relevant healthcare compliance standards. Exceptional leadership skills with the ability to inspire and guide cross-functional teams. Demonstrated history of leading Clinical organizations through significant change, including structural, cultural, and strategic change. Strategic mindset with the ability to align clinical objectives with business goals. Excellent communication and interpersonal skills, capable of representing the company in external settings. Requisition ID:592792 As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance… For full info follow application link. Boston Scientific is an Equal Opportunity Employer Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Disability, Veteran