About the role
AI summarisedThe Senior Clinical Innovation Manager at MedTech Catapult will lead the identification and validation of unmet clinical needs, translating them into product development and clinical trial strategies. This role involves managing complex projects, engaging stakeholders across the healthcare ecosystem, and ensuring compliance with regulatory and ethical standards. The ideal candidate has a PhD or degree in a relevant field and 5-7 years of experience in clinical innovation or medical device trials.
ResearchFull-timeMedTech Catapult
Key Responsibilities
- Identify and validate unmet clinical needs and translate them into viable project plans where clinical insights guide key user and design requirements.
- Provide expertise in clinical trial design, management, resourcing, regulatory pathways, procurement processes, and integration into hospital workflows.
- Engage clinical research organisations, clinicians, healthcare administrators, industry partners, and suppliers to accelerate translational success and adoption.
- Contribute to national efforts in clinical innovation, capability development, and knowledge sharing across the healthcare ecosystem.
- Ensure projects comply with clinical governance, ethical standards, and regulatory requirements.
- Prepare and review clinical and translational evidence to support market access and adoption milestones and/or decisions.
- Manage multiple projects concurrently with effective project planning and execution.
Requirements
- PhD or Degree in a relevant field (medicine, biomedical sciences, engineering, pharmacy, or related).
- Minimum 5 to 7 years of experience in clinical innovation, clinical operations, medical device trials and/or healthcare research.
- Strong knowledge of clinical governance, ethics, regulatory frameworks, procurement processes, and hospital operations.
- Demonstrated ability to translate clinical and scientific insights into product development and adoption strategies.
- Track record in supporting clinical innovation and clinical trials for FDA Class II and Class III medical devices preferred.
- Proven project management skills with experience managing diverse stakeholders and complex initiatives.
- Excellent communication and interpersonal skills with the ability to influence across clinical, industry, and policy stakeholders.