About the Role
Our client, a leading pharmaceutical company focused on developing innovative therapies, is seeking an experienced and proactive Clinical Project Manager . This critical role involves overseeing the planning, execution, and successful completion of clinical trials from initiation to close-out. You will manage project timelines, budgets, resources, and cross-functional teams to ensure trials are conducted in compliance with regulatory standards and company objectives. This position, based in Reading, Berkshire , offers a Hybrid working model, combining essential in-office collaboration with remote work flexibility. The ideal candidate will possess strong leadership skills, extensive knowledge of clinical trial management, and a proven track record of delivering complex projects on time and within budget. You will be instrumental in advancing our client's drug development pipeline.
Key Responsibilities
- Lead and manage all aspects of clinical trial execution, including planning, monitoring, and reporting.
- Develop and manage clinical trial budgets, timelines, and resource allocation.
- Oversee the selection and management of clinical trial sites and vendors.
- Ensure compliance with all applicable regulatory requirements (e.g., ICH-GCP, FDA, EMA) and company SOPs.
- Lead and motivate cross-functional project teams, including CRAs, data managers, statisticians, and medical monitors.
- Develop and execute risk management plans to mitigate potential project delays or issues.
- Serve as the primary point of contact for the project team and stakeholders, including regulatory authorities and external partners.
- Prepare and present project status reports, updates, and metrics to senior management.
- Manage the quality of trial data and ensure its integrity throughout the project lifecycle.
- Contribute to the development and continuous improvement of clinical operations processes and standards.
Requirements
- Bachelor's degree in a Life Science, Pharmacy, Nursing, or a related field. A Master's degree or PMP certification is a significant asset.
- Minimum of 5-7 years of experience in clinical trial management within the pharmaceutical or biotechnology industry.
- Demonstrated experience managing multiple complex clinical trials simultaneously.
- In-depth knowledge of clinical trial operations, regulatory guidelines (ICH-GCP), and drug development processes.
- Proven ability to manage project budgets, timelines, and resources effectively.
- Strong leadership, team management, and interpersonal skills.
- Excellent communication, presentation, and negotiation skills.
- Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC) systems, and project management software.
- Ability to work effectively in a hybrid environment, fostering collaboration both remotely and in-office.
- Strong problem-solving and decision-making capabilities.
Benefits
Our client offers a competitive salary, performance-based bonuses, and a comprehensive benefits package. This includes extensive health, dental, and vision insurance, as well as a company pension scheme. A generous annual leave allowance and other paid time off benefits are provided. Excellent opportunities for professional development, including advanced training and leadership programs, are available. The hybrid work model provides flexibility and promotes a healthy work-life balance. Join a dynamic and growing organization where your project management expertise will directly contribute to bringing life-changing medicines to patients.
