Future Tech Jobs
Future Tech Jobs
The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...
CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...
As a medical sales Account Manager covering parts of the Midlands & North, you’ll promote and grow the use of a specialist range of medical devices and cleanroom consumables across hospital pharmacy, aseptic compounding, oncology, infusion, and enteral feeding settings.*...
This role involves leading cross-functional teams in reviewing safety data, mentoring junior staff, and ensuring compliance with GxP guidelines and international regulations. The position also focuses on managing pharmacovigilance procedures, conducting impact assessments of new legislation, and supporting regulatory inspections and audits.
TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...
This role involves leading the design, execution, and reporting of post-authorisation safety studies using real-world data. The candidate will collaborate with various teams to produce high-quality evidence for regulatory decisions and risk management, ensuring AstraZeneca's medicines are safe and effective.
This role involves leading the global Discovery Chemistry and DMPK function within AstraZeneca's Oncology Targeted Delivery (OTD) organization. Responsibilities include setting strategic direction, driving innovation in small molecules, ADCs, and RCs, and fostering a high-performing, collaborative culture across R&D sites in Cambridge (UK), Cambridge (MA), and Gaithersburg (US).
This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.
The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global goals and regional requirements. This role involves close collaboration with global and local teams, providing regulatory expertise, anticipating risks, and driving timely submissions and approvals.
The Regional Regulatory Manager leads the development and execution of regional regulatory strategies for assigned assets, ensuring alignment with global strategies and regional requirements. This role involves close collaboration with global and local teams to deliver timely, compliant regulatory submissions and approvals, while providing regulatory expertise and market insights to support decision-making and risk management.
Medical Devices Project Leader - CambridgeWe are seeking a dynamic and driven Project Leader to join our innovative medical devices team based in Cambridge. This is a unique opportunity to lead cutting-edge development projects that directly impact patient care and...
The Field Technician will assist in troubleshooting, building, repairing, and testing electronic and medical equipment both in a workbench environment and on-site at customer locations. Key responsibilities include performing repairs, promoting service contracts, and supporting the warehouse and sales teams.
The Senior Scientific Writer II role involves developing high-quality medical and scientific communications for Novartis, including slide decks, congress materials, and advisory board content. The position requires strong collaboration with cross-functional teams to ensure content accuracy, consistency, and compliance with internal and external standards.
This senior role involves leading the scientific and operational aspects of complex, global early phase clinical trials. Responsibilities include designing and delivering high-quality studies, leading cross-functional teams, and ensuring robust data for key portfolio decisions. The role requires strong scientific and leadership skills, with a focus on continuous improvement and team collaboration.
As Head of Medicinal Chemistry, you will lead a team of 25 chemists in London, driving the development of novel drugs using cutting-edge AI and machine learning. You will provide strategic direction, mentor team members, and collaborate with AI/ML scientists to accelerate drug discovery and clinical candidate nomination.
This role involves managing the non-clinical aspects of IND submissions, including CMC, DMPK, pharmacology, and tox reporting. You will create and maintain detailed project plans, manage data and document workflows, and coordinate cross-functional teams to ensure regulatory compliance and successful submission.
This role involves leading a team of computational biologists to identify and advance novel oncology therapeutics. Responsibilities include mentoring team members, driving target discovery, defining patient population strategies, and collaborating with cross-functional teams to integrate and analyze complex biological data.
