Clinical Project Manager
A leading provider of advanced analytics research and technology solutions to the life sciences industry is seeking a Clinical Project Manager.
Key Responsibilities:
* Budget Management: Oversee clinical trials budget and ensure resources are allocated effectively, including staff, equipment, and supplies, while monitoring expenses and identifying cost-saving measures.
* Vendor/Staff Management: Recruit, train, and supervise vendors/staff, ensuring they follow GCP guidelines and other regulatory requirements.
* Data Integrity: Ensure the integrity and accuracy of clinical trial data by overseeing data management activities, including collection, analysis, and reporting, while ensuring data storage security and compliance with regulatory requirements.
* Quality Control: Develop and implement quality control measures to ensure compliance with regulatory requirements and standards.
* Stakeholder Liaison: Liaise with study CROs, principal investigators, and other stakeholders to provide regular updates on study progress and address any issues or concerns.
Your Background:
* Budgeting Knowledge: Strong understanding of budgeting and tracking principles.
* Safety and Ethics: Comprehensive knowledge of safety and ethics regulations.
* Site Management: Ability to coordinate site management with research activities.
* Industry Experience: Minimum 5+ years of experience in clinical trial management, preferably within outsourcing and contracts within the Pharmaceutical industry.
* Teamwork: Detail-oriented, analytical, and able to work effectively in a team environment.
About Our Client:
Our client offers research services and technology solutions in the life sciences industry, with operations in over 90 countries worldwide. They utilise artificial intelligence to optimise results of innovations and believe in maximising data usage rather than gathering information.
Location:
This role is a hybrid position, based at our client's sites in Paddington, London, and Basildon.