.Cdc Trial Manager Madrid, Community of Madrid Cdc Trial ManagerMadridMadrid, Community of Madrid, ES Are you passionate about Trial Management and would like to be part of the patient's life change? Do you want to be part of our Clinical Development Centre (CDC) team integrated by Spain and Portugal? If your answer is yes, don't hesitate and apply now to this unique opportunity!We are currently recruiting 2 Clinical Trial Manager for our Cardiovascular and RareDteams. Our office is in Madrid, but position could be based in anywhere in Spain. The Position As a Clinical Trial Manager working in the Cardiovascular Disease (CVD) or in Rare Diseases (RareD) team, you will use your project management skills to drive clinical trials in the CDC forward, making sure they are in accordance with the protocol, company policies, Standard Operating Procedures (SOPs), countries' legislation and ICH GCP requirements. You will be responsible for all the aspects of the clinical trials within the CDC project team of CRAs and CTAs, including strategy, country budget, recruitment, retention, risk analysis and management, database lock (DBL) and archiving. Your responsibilities will include:Project planning, management, and execution of assigned clinical trials in the CDC and adjacent affiliates in accordance with applicable regulatory requirements, NN Protocols and SOP's. Coordinating the CDC trial teams at a project levelwithin the 2 countries. To lead the project team, taking accountability for the trial budget, ensuring successful start-up clinical activities, setting project specific strategies and providing direction to ensure successful project delivery. Leading the planning, execution and communicating between relevant roles, such as CDC, Clinical Trial Assistants and Clinical Research Associates (CRA), as well as CRA coaching. To ensure effective communication of all trial related issues between the headquarters, CDC, other affiliates, and other internal/external stakeholders. To act as project manager for the trial management activities in the CDC from site selection to post-clinical trial activities. Representing CDC countries in study meetings as relevant: Country Calls, Monitor and Investigator meetings, Study Result meetings. Proactive risk identification and mitigation plans in the CDC level and adjacent affiliates. We are looking for a passionate and proactive solution-orientated professional able to coordinate tasks, identify potential risks as well as mitigations, effectively communicate between the Trial Squads, the Monitors (CRAs) and the Heads of Clinical/Clinical Research Managers to facilitate progress and global coordination of the clinical trial programme. Qualifications Minimum Bachelor's degree level in Life Sciences or equivalent Strong experience in Clinical Research, including at least 2 years in a Trial Management role. Experience with international clinical trials is desired for this positionStrategic and analytical mindset
