At a Glance
- Tasks: Develop and implement strategies to enhance patient recruitment and retention in clinical trials.
- Company: Join a leading global biopharmaceutical company with a focus on innovation.
- Benefits: Competitive salary, remote/hybrid work options, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on best practices and continuous improvement.
- Why this job: Make a real difference in global health by optimising clinical study delivery.
- Qualifications: Experience in Clinical Development and strong understanding of trial processes required.
The predicted salary is between 85000 - 90000 £ per year.
Cpl Life Sciences is partnering with a global biopharmaceutical company to appoint a Senior Manager within Trial Optimisation, with a particular focus on patient recruitment and retention. This is an opportunity to join a growing team supporting global clinical studies across a range of therapeutic areas. The role will focus on developing recruitment strategies, improving participant engagement, and working with internal and external stakeholders to optimise study delivery.
Key Responsibilities
- Develop and implement patient recruitment and retention strategies across global clinical studies.
- Partner with Clinical Operations, Medical Affairs, Study Management and Feasibility teams to support study enrolment goals.
- Conduct country feasibility assessments and evaluate operational landscapes to support country and site selection.
- Work closely with CROs, recruitment vendors and patient engagement partners to deliver recruitment initiatives.
- Provide patient and site insights to support protocol development and improve the participant experience.
- Identify recruitment risks and develop mitigation plans to minimise impact on study timelines.
- Analyse recruitment and operational data to support decision-making and study optimisation.
- Monitor study performance and recommend actions to improve enrolment and retention outcomes.
- Support process improvement initiatives and contribute to best practice across trial optimisation activities.
Requirements
- Experience within Clinical Development, Clinical Operations, Feasibility, Patient Recruitment or Trial Optimisation.
- Strong understanding of global clinical trial processes and patient recruitment strategies.
- Experience working with CROs, vendors and cross-functional teams.
- Ability to interpret data and translate findings into practical recommendations.
For further information or a confidential discussion, please apply or contact sarah.phillips@cpl.com.
Senior Manager of Clinical Trial Optimisation employer: Cpl Life Sciences
Cpl Life Sciences is an exceptional employer, offering a dynamic work environment that fosters collaboration and innovation in the biopharmaceutical sector. With a strong focus on employee growth, you will have access to professional development opportunities while working remotely or in a hybrid setting, allowing for a healthy work-life balance. Join us to make a meaningful impact on global clinical studies and be part of a supportive team dedicated to optimising patient recruitment and retention.
