Graduate jobs in Gran Bretaña

Location: London, UK

Reporting to: Director, Clinical Development

Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the development of innovative cell and gene therapies. Orchard has its global headquarters in London and its U.S. headquarters in Boston and is a wholly owned subsidiary of Kyowa Kirin, a Japan-based Global Specialty Pharmaceutical Company.

The Senior Manager, Clinical Development will play a key role in shaping and driving one or more of Orchard’s clinical development programs, by supporting the clinical development lead for that program. They will support the development and execution of clinical strategies that align with the company’s scientific and regulatory goals. They will also support regulatory interactions across all phases of development, from early clinical trials to regulatory approval and ongoing post-marketing commitments.

This is a unique opportunity to join a dynamic, forward-thinking team committed to advancing innovative therapies that have the potential to transform patient lives. This role is ideal for a medically trained professional early in their career who is eager to gain hands‑on experience in clinical drug development within a dynamic biotech environment.

• Support the development and execution of robust clinical plans that meet scientific objectives, align with regulatory requirements across all participating regions, and deliver high‑quality data for timely asset delivery.
• Medical oversight and input to clinical trial design, conduct, and data interpretation, working closely with cross‑functional teams—including clinical operations, regulatory affairs, pharmacovigilance, and biostatistics.
• Collaborate with clinical operations and pharmacovigilance to ensure study integrity and subject safety.
• Maintain close communication and collaboration with clinical sites and physicians, gaining insight into study design, identifying, and leading solutions for study issues.
• Leading and ensuring development, review, finalization and delivery of high‑quality key clinical study documents, including protocol, IB, CSRs, committee charters, SOPs and other compliance documents, where required, to meet study timelines.
• Support the clinical lead in regulatory interactions – both written and verbal (meetings).
• Key author in the strategic writing and review of clinical sections of regulatory documents and regulatory interactions (INDs, CTA submissions, information requests).
• Act as the medical monitor for one or more programs, overseeing CRO medical monitoring, and providing medical input and expertise, including collaboration with pharmacovigilance.
• Maintain up‑to‑date knowledge of the scientific literature, competitive landscape, and regulatory requirements within relevant therapeutic areas.
• Work cross‑functionally to maintain critical overview of study related activities including SAE/stopping criteria, signal detection, data management/stats analysis, etc; as well as planning investigators meetings, kick‑off meetings, and similar forums for study activities discussions.
• Contribute to the development and maintenance of the clinical sciences budget for associated assets/activities, ensuring cost effectiveness and addressing and escalating issues as appropriate.
• Interact with various vendors in support of clinical development programs.
• Participate in publication plans and execution, as required.
• Ensure accurate maintenance and archiving of study records.
• Support the development of clinical development project plans, management of risk, monitoring of progress, and implementation of contingencies as required. Support the efficient use of resources and adherence to strategic initiatives.
• Ensure adherence to Good Clinical Practice and all applicable local and international regulations.
• Participate in business development initiatives for new programmes, as required.
• Present at internal and external meetings, congresses as required.

• Understanding of stages of clinical development, and fundamentals of data interpretation from clinical studies.
• Proven experience in cross functional working, problem solving, collaboration at the academia/CRO/sponsor interface.
• Collaborating with external partners, including investigators, academic partners, and vendors.
• Understanding of regulatory environment, GCP/ICH.
• Gene therapy / paediatrics / neurometabolic diseases / neurology / rare disease background desired.
• The position will suit a physician newly moving into the pharmaceutical industry, with prior CRO or clinical trial experience, or with a number of years of experience within a sponsor company.

• Scientific curiosity and analytical mindset, strong attention to detail and documentation, strong ethical judgment and patient focus.
• Mature thinker, who takes accountability and is capable of working independently to make robust decisions, as well as awareness of when and how to elevate topics for senior input when needed.
• Strong communication (written and verbal) and presentation skills (including PowerPoint proficiency), enabling efficient sharing of information in external, internal, group, and 1:1 setting and ability to respond to questions in real time with clarity and composure.
• A high achiever with the ability and desire to work in a fast‑paced and highly dynamic environment. ‘Can‑do’ attitude and willingness to be flexible at short notice and adjust according to changing demands.
• Proactivity – pragmatic identification of issues, taking ownership of routes to solution without prompting.
• Strong leadership skills – able to lead workstreams and influence across cross functional teams.
• Collaborative working style; the ideal candidate will partner effectively with their colleagues across the organization to seek critical information, constructively challenge plans and assist with the optimal allocation of resources.
• Excellent organisational skills: able to prioritise activities depending on business imperative and to contribute to multiple projects in parallel.
• Able to work and navigate the complexities of academic/biotech interface.
• Able to work in a virtual enterprise.
• Data interpretation and critical analysis skills.

• Medical degree essential, with at least 4 years of clinical work following qualification. Ideally with a relevant post‑graduate qualification (e.g., MRCP, MRCS, MFPM, MD, PhD).