Senior Global Clinical Project Manager

• Job title: Senior Global Clinical Project Manager

• Company: Biotechnology

• Location: London Area (Hybrid)

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We’re looking for a Senior Clinical Project Leader who can work independently and take charge of global clinical trials from start to finish. You'll be responsible for timelines, budgets, and making sure everything runs smoothly according to the company SOPs and ICH/GCP guidelines. This includes both in-house studies and those outsourced to CROs. You'll also help drive process improvements.

This role is within an ambitious Biotechnology company with a low staff turnover rate. They pay higher than the industry average in the study management space and have great opportunities for personal development. The team is very collaborative and passionate about their research.

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What You'll Do:

• Lead the cross-functional team for clinical study delivery and be the main point of contact.

• Provide operational input into protocol development.

• Oversee the creation of study documents like case report forms, data management plans, monitoring plans, and more.

• Manage study systems like CTMS and TMF.

• Ensure compliance with clinical trial registry requirements.

• Identify outsourcing needs and manage vendor contracts.

• Develop and manage study budgets and timelines.

• Assess risks and create mitigation strategies.

• Select regions and countries for the study.

• Conduct site evaluations and selections.

• Prepare and execute investigator meetings.

• Monitor site activation and visits, addressing any deviations.

• Develop and implement patient recruitment and retention strategies.

• Monitor data entry and query resolution.

• Manage budgets and scope changes.

• Forecast and manage study drug and clinical supplies.

• Escalate issues related to study conduct, quality, timelines, or budget.

• Ensure CROs and vendors are aligned and delivering as expected.

• Maintain audit and inspection readiness throughout the study lifecycle.

• Support internal audits and external inspections.

• Manage study close-out activities like database lock and vendor contract reconciliation.

• Contribute to clinical study report writing and review.

• Facilitate study-level lessons learned.

• Assign tasks to Clinical Study Management staff and support their deliverables.

• Participate in process improvement initiatives.

• Identify innovative approaches to clinical study execution.

• Handle unmasked tasks for studies, including investigational product management and data review.

• Supervise CTM staff, including work assignments, performance management, recruitment, and training.

To apply:

If you would like to discuss this vacancy further or to discuss your career options in confidence, please click ‘apply’ or contact Joe Pearce for any further information

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About RBW Consulting

RBW Consulting is a life sciences talent & strategic consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We’ve created a culture rooted in support, transparency and mutual commitment. We lead with our values from the inside; empowering and investing in our people is more important than short-term commercial gain.

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We are an equal opportunities Recruitment Business and Agency

RBW Consulting is an equal opportunity workplace. We prioritize talent (both current and potential) over resumes, challenge the status quo, and value people as our most important asset. We do not discriminate on the basis of race, ethnicity, colour, sex, gender identity or expression, sexual orientation, religion, age, marital status, visible or invisible disability, medical condition, national origin, veteran status, or any other protected status. We strive to be a diverse workforce that is representative at all levels and are committed to building a team that represents a variety of backgrounds, perspectives, and skills.