96 Clinical Trials jobs in London

Job Title: Deputy Production Manager

Company: Leading UK Clinical Research Organisation

Location: London, UK

Working Schedule: Full-time – On-site

Start Date: ASAP

About the Company

This organisation is one of the UK’s leading independent early-phase clinical research centres. They have built a strong reputation for running safe, high-quality Phase I trials with biotech and pharma partners worldwide. The pharmacy and production teams are central to this mission, preparing and managing investigational medicines under strict GMP.

The company is also in an exciting period of expansion . Facility upgrades are already underway, with further improvements due over the next 1–2 years. These will bring new capabilities, enhanced staff benefits, and a modernised GMP environment. Joining now means being part of that journey – shaping processes, influencing standards, and playing a direct role in how the pharmacy function grows.

The Role

We’re looking for a Deputy Production Manager to join the pharmacy team. This is a senior production role, ideal for someone with aseptic training and strong production management experience. You’ll deputise for the Production Manager, lead technicians, and ensure the highest GMP standards across sterile and non-sterile manufacturing.

Key responsibilities include:

• Leading the day-to-day management of the production team, including rotas and capacity planning.
• Writing, reviewing, and maintaining SOPs.
• Overseeing preparation of sterile and non-sterile formulations (suspensions, solutions, capsules).
• Managing environmental monitoring and aseptic operations.
• Representing pharmacy during audits and inspections.
• Mentoring technicians and apprentices, ensuring compliance and quality standards.
• Supporting the Production Manager with scheduling, documentation, and sponsor liaison.

You’ll work closely with QA and clinical operations, reporting directly into the Principal Pharmacist & Production Manager.

Key Requirements

We’re ideally looking for someone with:

• A science-based degree (pharmacy, pharmaceutical sciences, microbiology, or similar).
• Strong GMP knowledge with hands-on aseptic/sterile manufacturing experience.
• Experience preparing sterile and non-sterile medicines (solutions, suspensions, capsules).
• Previous supervisory or management experience in a GMP environment.
• Ability to write, review, and maintain SOPs.
• Confident with documentation, email communication, and regulatory standards.
• GPhC registration preferred but not essential if equivalent GMP aseptic production experience can be demonstrated.

What’s on Offer

• 25 days annual leave, pension, and overtime pay.
• A collaborative, supportive environment with fast feedback and interview turnaround.
• The chance to play a visible, high-responsibility role in shaping early-phase clinical research.

Job Title: Deputy Production Manager

Company: Leading UK Clinical Research Organisation

Location: London, UK

Working Schedule: Full-time – On-site

Start Date: ASAP

About the Company

This organisation is one of the UK’s leading independent early-phase clinical research centres. They have built a strong reputation for running safe, high-quality Phase I trials with biotech and pharma partners worldwide. The pharmacy and production teams are central to this mission, preparing and managing investigational medicines under strict GMP.

The company is also in an exciting period of expansion . Facility upgrades are already underway, with further improvements due over the next 1–2 years. These will bring new capabilities, enhanced staff benefits, and a modernised GMP environment. Joining now means being part of that journey – shaping processes, influencing standards, and playing a direct role in how the pharmacy function grows.

The Role

We’re looking for a Deputy Production Manager to join the pharmacy team. This is a senior production role, ideal for someone with aseptic training and strong production management experience. You’ll deputise for the Production Manager, lead technicians, and ensure the highest GMP standards across sterile and non-sterile manufacturing.

Key responsibilities include:

• Leading the day-to-day management of the production team, including rotas and capacity planning.
• Writing, reviewing, and maintaining SOPs.
• Overseeing preparation of sterile and non-sterile formulations (suspensions, solutions, capsules).
• Managing environmental monitoring and aseptic operations.
• Representing pharmacy during audits and inspections.
• Mentoring technicians and apprentices, ensuring compliance and quality standards.
• Supporting the Production Manager with scheduling, documentation, and sponsor liaison.

You’ll work closely with QA and clinical operations, reporting directly into the Principal Pharmacist & Production Manager.

Key Requirements

We’re ideally looking for someone with:

• A science-based degree (pharmacy, pharmaceutical sciences, microbiology, or similar).
• Strong GMP knowledge with hands-on aseptic/sterile manufacturing experience.
• Experience preparing sterile and non-sterile medicines (solutions, suspensions, capsules).
• Previous supervisory or management experience in a GMP environment.
• Ability to write, review, and maintain SOPs.
• Confident with documentation, email communication, and regulatory standards.
• GPhC registration preferred but not essential if equivalent GMP aseptic production experience can be demonstrated.

What’s on Offer

• 25 days annual leave, pension, and overtime pay.
• A collaborative, supportive environment with fast feedback and interview turnaround.
• The chance to play a visible, high-responsibility role in shaping early-phase clinical research.

• Conduct site initiation, interim monitoring, and close-out visits in accordance with Good Clinical Practice (GCP) and protocol requirements.
• Ensure the quality, accuracy, and integrity of clinical data collected at investigational sites.
• Verify that all investigational sites are adequately supplied with study supplies and informed about protocol requirements.
• Oversee patient recruitment and retention efforts at assigned clinical sites.
• Build and maintain strong working relationships with investigators, site staff, and other stakeholders.
• Ensure compliance with all applicable regulatory requirements (e.g., FDA, EMA) and internal company policies.
• Prepare and present study-related materials to site staff during initiation visits and regular calls.
• Identify and resolve site-level issues and escalate critical problems as necessary.
• Review and approve site visit reports and other study documentation.
• Contribute to the development of clinical trial protocols, case report forms (CRFs), and other study documents.
• Manage multiple clinical trials and study sites concurrently.
• Stay updated on oncology research trends and regulatory guidelines.

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; Master's degree or equivalent experience preferred.
• Minimum of 5 years of progressive experience as a Clinical Research Associate, with a significant focus on oncology trials.
• Thorough understanding of GCP, ICH guidelines, and relevant regulatory requirements.
• Demonstrated experience in monitoring clinical trials from initiation to close-out.
• Excellent knowledge of oncology drug development and clinical trial designs.
• Strong analytical and problem-solving skills with meticulous attention to detail.
• Exceptional communication, interpersonal, and negotiation skills.
• Ability to travel to clinical sites as required (approximately 40-60% travel).
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Ability to work independently and manage time effectively.
• A proactive approach to problem-solving and a commitment to patient safety and data integrity.

We are seeking an experienced Clinical Trial Manager to join a London-based biotech and lead the planning, execution, and delivery of clinical trials. The successful candidate will excel in fast-paced, dynamic biotech settings and be committed to driving trials that meet the highest standards of quality, compliance, and operational excellence.

Responsibilities:

• Lead the design, start-up, and execution of clinical trials, ensuring projects are completed on schedule, within scope, and aligned with budgetary expectations.
• Serve as the primary sponsor contact for CROs, investigators, and providers.
• Oversee CRO performance, including reviewing monitoring outputs and KPIs.
• Work closely with Regulatory Affairs on ethics/regulatory submissions, ensuring alignment with ICH-GCP guidelines and current UK/EU regulations.
• Maintain trial inspection readiness, overseeing safety reporting, audit response, and vendor governance.
• Develop and review protocols, informed consent forms, and study reports.
• Drive risk management, issue resolution, and collaboration across cross-functional teams.
• Play an active role in refining operational processes and SOPs within the Clinical Operations function.

Requirements:

• Bachelor’s degree (or equivalent) in a life science or health-related discipline.
• Minimum of 8 years in clinical trial management across pharma, biotech, or CROs.
• Site monitoring experience or proven ability to critically evaluate CRO monitoring performance.
• In-depth understanding of ICH-GCP and global regulatory requirements, with strong understanding of upcoming UK/EU regulatory changes (e.g., UK CTR 2026).
• Demonstrated success in managing CROs and vendors, including financial oversight.
• Skilled at balancing multiple priorities and tight timelines.
• Proficient in navigating lean, fast-paced environments; direct experience in biotech settings is valued.
• Strong interpersonal and communication skills, with proven ability to manage internal stakeholders with accountability and transparency.
• Able to work on-site in central London in a hybrid capacity.

We are seeking an experienced Clinical Trial Manager to join a London-based biotech and lead the planning, execution, and delivery of clinical trials. The successful candidate will excel in fast-paced, dynamic biotech settings and be committed to driving trials that meet the highest standards of quality, compliance, and operational excellence.

Responsibilities:

• Lead the design, start-up, and execution of clinical trials, ensuring projects are completed on schedule, within scope, and aligned with budgetary expectations.
• Serve as the primary sponsor contact for CROs, investigators, and providers.
• Oversee CRO performance, including reviewing monitoring outputs and KPIs.
• Work closely with Regulatory Affairs on ethics/regulatory submissions, ensuring alignment with ICH-GCP guidelines and current UK/EU regulations.
• Maintain trial inspection readiness, overseeing safety reporting, audit response, and vendor governance.
• Develop and review protocols, informed consent forms, and study reports.
• Drive risk management, issue resolution, and collaboration across cross-functional teams.
• Play an active role in refining operational processes and SOPs within the Clinical Operations function.

Requirements:

• Bachelor’s degree (or equivalent) in a life science or health-related discipline.
• Minimum of 8 years in clinical trial management across pharma, biotech, or CROs.
• Site monitoring experience or proven ability to critically evaluate CRO monitoring performance.
• In-depth understanding of ICH-GCP and global regulatory requirements, with strong understanding of upcoming UK/EU regulatory changes (e.g., UK CTR 2026).
• Demonstrated success in managing CROs and vendors, including financial oversight.
• Skilled at balancing multiple priorities and tight timelines.
• Proficient in navigating lean, fast-paced environments; direct experience in biotech settings is valued.
• Strong interpersonal and communication skills, with proven ability to manage internal stakeholders with accountability and transparency.
• Able to work on-site in central London in a hybrid capacity.

Hobson Prior is seeking a Clinical Trial Supply Manager to join a dynamic team in Uxbridge, UK. In this role, you will play a key part in managing the supply chain for investigational products, ensuring timely delivery and alignment with clinical study goals. This position involves collaboration with internal teams and external partners to support global clinical trials in the cell and gene therapy/biologics space.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Develop and maintain supply strategies for investigational products based on clinical and regulatory requirements.
• Work closely with internal teams and external vendors to ensure all supply needs are met.
• Plan and communicate supply chain strategies to align with clinical study objectives.
• Monitor inventory, analyze drug usage, and adjust forecasts as needed.
• Oversee manufacturing, packaging, and labeling requests to meet protocol and regulatory standards.
• Support use date extensions and ensure compliance with country-specific regulations.
• Participate in meetings to provide updates, highlight risks, and propose mitigation strategies.
• Manage distribution strategies and maintain supply levels at depots and clinical sites.
• Collaborate on budget planning and procurement of commercial drugs.
• Act as the primary contact for clinical supply matters related to assigned studies.
• Ensure inspection readiness by preparing necessary documentation and addressing product complaints or deviations.

Key Skills and Requirements:

• Strong understanding of global drug development processes and regulatory requirements.
• Proficient in forecasting, planning, and supply chain management.
• Knowledge of manufacturing, packaging, labeling, and logistics processes.
• Familiarity with industry systems such as IVRS and CTMS.
• Excellent communication, negotiation, and project management skills.
• Ability to analyze issues, resolve conflicts, and build consensus within teams.
• Experience in managing budgets and working with external vendors.

For more information, please contact Emma Miles .

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -

Hobson Prior is seeking a Clinical Trial Supply Manager to join a dynamic team in Uxbridge, UK. In this role, you will play a key part in managing the supply chain for investigational products, ensuring timely delivery and alignment with clinical study goals. This position involves collaboration with internal teams and external partners to support global clinical trials in the cell and gene therapy/biologics space.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Develop and maintain supply strategies for investigational products based on clinical and regulatory requirements.
• Work closely with internal teams and external vendors to ensure all supply needs are met.
• Plan and communicate supply chain strategies to align with clinical study objectives.
• Monitor inventory, analyze drug usage, and adjust forecasts as needed.
• Oversee manufacturing, packaging, and labeling requests to meet protocol and regulatory standards.
• Support use date extensions and ensure compliance with country-specific regulations.
• Participate in meetings to provide updates, highlight risks, and propose mitigation strategies.
• Manage distribution strategies and maintain supply levels at depots and clinical sites.
• Collaborate on budget planning and procurement of commercial drugs.
• Act as the primary contact for clinical supply matters related to assigned studies.
• Ensure inspection readiness by preparing necessary documentation and addressing product complaints or deviations.

Key Skills and Requirements:

• Strong understanding of global drug development processes and regulatory requirements.
• Proficient in forecasting, planning, and supply chain management.
• Knowledge of manufacturing, packaging, labeling, and logistics processes.
• Familiarity with industry systems such as IVRS and CTMS.
• Excellent communication, negotiation, and project management skills.
• Ability to analyze issues, resolve conflicts, and build consensus within teams.
• Experience in managing budgets and working with external vendors.

For more information, please contact Emma Miles .

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - -policy.