This role involves leading epidemiology programs, designing and delivering observational studies using real-world data, and providing scientific advice to cross-functional teams. The position offers opportunities for growth and impact in a hybrid working environment.
This role involves leading epidemiology programs, designing and delivering observational studies using real-world data, and collaborating with cross-functional teams. The position offers opportunities for growth and impact in the development and lifecycle of medical products.
This role involves providing technical leadership for facility and utility systems at Moderna’s new biotech site in Harwell, Oxford. The Facilities Engineering Manager will oversee maintenance, vendor performance, and engineering projects across R&D and manufacturing environments, ensuring compliance and operational reliability. The position emphasizes continuous improvement, digital tool integration, and collaboration with global teams in a GMP-regulated setting.
This role involves providing technical leadership for facility and utility systems at Moderna’s biotech manufacturing site in Harwell. The Facilities Engineering Manager ensures operational reliability, oversees vendor performance, and drives maintenance excellence across R&D and manufacturing environments. The position emphasizes continuous improvement, compliance, and the use of digital tools including AI-enabled systems, within a GMP-regulated setting.
The role involves end-to-end management of clinical trials within a fast-paced, AI-driven drug discovery environment. The Senior Clinical Trial Manager will lead cross-functional teams, oversee trial start-up through close-out, ensure compliance with ICH/GCP standards, and integrate AI innovations into clinical operations. Key responsibilities include vendor and budget management, clinical documentation, data oversight, and supporting regulatory readiness and audits.
Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.
This role involves joining Recursion's Internship Talent Network to be considered for future internship opportunities within a TechBio company focused on AI-driven drug discovery. Interns will engage with a platform that integrates biology, chemistry, and clinical development using proprietary AI models and large-scale automated laboratories. The position emphasizes innovation, cross-functional collaboration, and rapid learning in a mission-driven environment aimed at addressing significant unmet medical needs.
This role involves leading chemical biology efforts at Recursion, developing strategies for chemical probe design, and managing a team of chemists. The position focuses on integrating AI/ML-driven platforms to advance drug discovery and target identification, working closely with multidisciplinary teams.
The Central Monitor (CM) oversees and supports clinical trials through centralized monitoring activities, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure Central Monitoring technology, and provide ongoing data surveillance and risk management.
This role involves leading early-phase clinical development (Phase 1 and 2) of novel gastroenterology therapies, with a focus on inflammatory bowel disease (IBD). The Translational Medicine Expert will design clinical development plans, serve as medical lead for trials, and collaborate closely with research, biomarker, and late-phase development teams. The position requires strong scientific leadership, engagement with key opinion leaders, and active involvement in regulatory interactions.
Lead the development of medical devices from concept to commercial launch within a multidisciplinary engineering team. Provide technical leadership, mentor junior engineers, and ensure robust design and compliance, particularly for products involving injection-moulded plastic components. Contribute to regulatory strategy and full lifecycle development in a fast-paced environment focused on improving patient outcomes.
The Process/Equipment Engineer provides technical support for the Bio-Vaccines Suites, ensuring equipment reliability and resolving manufacturing issues. Responsibilities include troubleshooting, leading investigations, validation, compliance, and continuous improvement initiatives.
This role involves supporting the clinical development of vaccines through various activities, including protocol development, regulatory compliance, data review, and medical oversight. The position provides hands-on experience in a busy clinical research environment, contributing to global vaccine programs and promoting STEM activities.
Operate and monitor manufacturing processes in a cGMP-regulated biopharmaceutical environment, supporting the production of life-changing medicines. Perform troubleshooting, contribute to process improvements using Lean methodologies, and assist in validation and documentation activities. Work within a rotating shift pattern in a safety-focused, highly regulated team setting.
