Medical Director

• Act as a trusted partner to Country Business Leaders, contributing to strategic decision-making
• Understand the needs of diverse clinical and non-clinical stakeholders across the healthcare ecosystem
• Build and maintain strong external relationships with key stakeholders, including Strategic Accounts, Hospital Groups, Regulatory Authorities, and Medical Societies
• Develop and nurture partnerships with customers, with a strong focus on identifying, engaging, and developing Key Opinion Leaders (KOLs)
• Identify and establish strategic collaborations that drive growth across core business areas
• Ensure that evidence supporting J&J MedTech products and services is robust, relevant, and aligned with country requirements
• Drive clear, credible, and impactful communication of scientific and clinical evidence
• Anticipate healthcare trends, policy developments, and changes in the healthcare ecosystem to inform strategic direction
• Collaborate with Global Franchise Medical Affairs teams to shape the global innovation agenda through customer insights and identification of unmet needs
• Support the execution of evidence plans, including case support and identification of data generation opportunities
• Contribute to and execute the evidence dissemination strategy, ensuring translation of evidence into clinical practice
• Provide scientific and medical leadership within areas of surgical expertise to support business priorities
• Facilitate scientific exchange through medical education activities, congress participation, and expert engagement

Medical Affairs Director

• Lead the end-to-end strategy and execution of assigned renal clinical development program(s) across the full Research, Development and Commercial (RDC) continuum; from early development through pivotal/registrational phases
• Providing clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program
• Leading development of clinical sections of trial and program level regulatory documents
• Driving execution of the assigned clinical program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, where applicable
• Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall program safety reporting in collaboration with Patient Safety colleagues
• Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas
• As a medical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards
• May work with BR (Biomedical Research/ Translational Medical Sciences) to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L (Business Development & Licensing) including target identification and due diligences together with other medical matters, as needed.

Senior Clinical Development Medical Director – Renal

• Serve primarily as a Medical Monitor (MM) with the main responsibility of developing, setting up, managing, and reporting out data from Phase 1-4 clinical trial protocols
• Contribute to study protocol development concepts and protocol writing
• Provide medical perspective on overall study conduct, procedures, and management of safety events to clinical study team
• Provide daily medical oversight to study participants enrolled in clinical trials including answering questions regarding patient care that arise from the study site or the Principal Investigator
• Support and contribute to regulatory filings to U.S. and international health authorities both during and after trial conduct

• Lead and deliver the clinical strategy across Clinics & Specialist Primary Care, working closely with service line directors
• Ensure services are consistently rated ‘Good’ or above by the CQC and comply with Bupa clinical governance and risk standards
• Act as the clinical voice on the Clinics Leadership Team, contributing to strategic and operational decision-making
• Attract, develop and retain high-calibre clinical professionals across multiple specialties
• Ensure robust clinical governance, performance management and management of clinical outliers
• Work with Innovation and Product teams to develop new pathways and services that enhance patient outcomes
• Oversee the collection and use of clinical outcomes, PROMs and PREMs to evidence quality and value
• Support sales and marketing activity by articulating Bupa’s clinical excellence and expertise

Medical Director – Clinics

• Define and drive the clinical strategy for the assigned care area (molecular imaging)
• Lead the development of Target Product Profiles (TPPs)
• Represent the therapeutic area in governance forums and regulatory interactions
• Engage with KOLs and external experts to shape development strategy
• Oversee cross-functional alignment across Regulatory, Medical Affairs, Commercial, and Clinical Operations
• Mentor and guide clinical scientists and medical monitors working within the care area
• Provide medical oversight for one or more clinical trials
• Review safety data, assess adverse events, and support dose modifications or protocol amendments
• Respond to investigator queries and support site engagement
• Participate in Data Safety Monitoring Boards (DSMBs) and internal safety reviews
• Contribute to clinical study reports (CSRs), regulatory submissions, and medical writing
• Collaborate with Clinical Operations and Pharmacovigilance teams

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Medical Affairs Director

Senior Clinical Development Medical Director – Renal

Medical Director

Medical Director – Clinics

Senior Medical Director