Beatriz Sarrión Valero

Line Manager of 20 Clinical Research Associates with the below main responsibilities:

• Generate action plans and provide strategic oversight to optimize CRA services.
• Assist with and contribute to project resourcing to ensure proper level and allocation resource is assigned for each project.
• Collaborate with the Clinical Team Leads and Clinical Operations Management Team to ensure that resource needs and site requirements are met appropriately.
• Develop, mentor, manage and coach CRA staff to progress their skills.
• Perform accompanied site visits to assess CRA skills and developmental needs.
• Identify quality risks and issues and recommend corrective action plans as needed to leadership team to address deficiencies in performance of employees.
• Work with the Clinical Operations Management Team to continually improve and enhance CRA expectations and procedures to promote quality, consistency and efficiency in execution.
• Develop and maintain metrics pertinent to CRA resource oversight.
• Participate in the interview process for new CRAs by conducting CV review and participating in the interviewing process.
• Conduct on-boarding training for new CRA staff in conjunction with relevant company team.

Working al Global Lead CRA managing international projects.

Also acting as Line Manager supervising, mentoring and managing of 5 CRAs.

Main responsibilities:

• Management and operational delivery of the clinical elements within a trial including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning activities and close-out.
• Successful execution of assigned trials and ensuring completion of trial deliverables.
• Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trials by working in close collaboration with other functional team members.
• Mentoring and training of team members.
• Identify challenges to study timelines/deliverables and offer creative action plans to the team/sponsor
• Lead CRAs as they establish relationships with their sites for high quality oversight of monitoring, regulatory, IP, site payment and overall site correspondence activities.
• Maintain team focus on study priorities through efficient cross-functional partnerships and effective communication to achieve the highest level of client satisfaction.