Future Tech Jobs
Future Tech Jobs
This role involves leading medical oversight in oncology clinical development, focusing on hematology and clonal myeloid disorders. The Medical Director will guide study design, ensure patient safety, interpret clinical data, and collaborate with cross-functional teams and external experts. It is a physician-led position embedded in clinical strategy with a strong emphasis on real-world impact and regulatory engagement.
This role involves providing medical leadership within GSK's oncology clinical development team, focusing on genitourinary (GU) cancers. The Medical Director will lead medical monitoring, ensure patient safety, interpret clinical data, and contribute to study design and regulatory submissions. Working closely with cross-functional teams, the role integrates physician-level insight into clinical strategy and drug development execution.
Leads scientific components of oncology clinical studies, contributing to protocol design, data interpretation, and regulatory documentation within a defined clinical programme. Works closely with cross-functional teams to ensure scientific rigor and alignment with development goals. Focuses on generating robust clinical insights to advance cancer therapies in high unmet need areas.
Provides scientific leadership in oncology clinical development, contributing to study design, data interpretation, and regulatory deliverables within a defined clinical programme. Works closely with cross-functional teams and external experts to ensure scientific rigor and data integrity. Focuses on advancing cancer therapies with high unmet need through robust clinical science and collaboration.
This role involves providing medical leadership in oncology clinical development, with responsibilities spanning study design, medical monitoring, safety oversight, and data interpretation. The Medical Director will integrate physician-level insights into clinical trials, collaborate with cross-functional teams and external experts, and contribute to regulatory submissions and scientific communications. The position emphasizes patient-centered decision-making and real-world impact in cancer treatment innovation.
Leads clinical development strategy for oncology assets focused on lung and head/neck cancers, defining the scientific narrative, benefit-risk framework, and decision pathways across the asset lifecycle. Serves as the primary clinical authority, representing Clinical Development in governance, regulatory interactions, and cross-functional strategy. Leverages advanced analytics and AI to drive data-informed decisions and mentors clinical talent within a global R&D environment.
Lead the design and execution of real-world evidence (RWE) and health outcomes studies to support GSK's hepatology assets across the product lifecycle. Drive scientific credibility in value-based evidence generation, aligning with regulatory, reimbursement, and payer requirements. Collaborate with cross-functional teams and external experts to translate evidence needs into impactful research strategies.
Leads a global team responsible for developing and managing regulatory labelling strategies for oncology products across the drug development lifecycle. Ensures compliance with global regulations, collaborates with cross-functional stakeholders in R&D, safety, and commercial teams, and engages with regulatory authorities to shape innovative, patient-focused labelling. Plays a strategic role in governance and policy development within GSK’s oncology portfolio.
Leads clinical development strategy for oncology assets focused on lung and head/neck cancers, defining the scientific narrative, benefit-risk framework, and decision-making roadmap across the asset lifecycle. Serves as the primary clinical authority within cross-functional teams and external engagements, leveraging advanced analytics and AI-driven insights to accelerate development. Focuses on integrating clinical, regulatory, and commercial strategies to deliver impactful medicines for high-unmet-need cancers.
Leads clinical development strategy for oncology assets focused on lung and head/neck cancers, defining the scientific narrative, benefit-risk framework, and decision pathways across the asset lifecycle. Acts as the primary clinical authority, shaping strategic direction, engaging with health authorities, and integrating AI and advanced analytics to accelerate development. Mentors clinical talent and ensures alignment across regulatory, commercial, and scientific functions to drive impactful patient outcomes.
Leads clinical development strategy for oncology assets focused on lung and head/neck cancers, defining the scientific narrative, benefit-risk framework, and governance decisions across the asset lifecycle. Serves as the primary clinical authority, integrating clinical, regulatory, and commercial considerations while leveraging advanced analytics and AI to accelerate development. Provides strategic direction to study teams and represents Clinical Development in internal governance and external engagements.
This role leads clinical strategy and scientific vision for oncology assets focused on lung and head/neck cancers, shaping end-to-end development from discovery to real-world impact. The Executive Medical Director acts as a strategic leader within cross-functional teams, drives governance decisions, and leverages advanced analytics and AI to accelerate clinical development. They represent Clinical Development in regulatory and external engagements while mentoring talent and advancing integrated, data-driven approaches across the asset lifecycle.
Leads clinical development strategy for oncology assets focused on lung and head/neck cancers, defining the scientific narrative, benefit-risk framework, and decision pathways across the asset lifecycle. Acts as the primary clinical authority, shaping strategic direction, engaging with health authorities, and leveraging advanced analytics to accelerate development. Mentors clinical talent and drives integrated, data-driven decision-making across cross-functional teams.
Leads the design and execution of real-world evidence and health outcomes research studies to support GSK's hepatology assets. Works cross-functionally to align evidence generation with regulatory, reimbursement, and market access needs, ensuring robust data supports product value and patient access. Engages with internal teams and external experts to translate scientific insights into impactful health outcomes strategies.
Lead the design and execution of real-world evidence and health outcomes research studies to support GSK's hepatology assets, ensuring robust data for market access and reimbursement. Collaborate with cross-functional teams and external experts to generate impactful evidence on product value. Drive scientific credibility in study planning, analysis, and dissemination across the product lifecycle.
