Parexel

Compensation

Full Description

Job Description: • Oversee the management and leadership of Parexel's Patient Safety pillar • Work with senior management, customers, business development, and project teams providing oversight of processes and functions related to Patient Safety Services • Lead operational level planning with significant business oversight • Drive positive change through continuous process improvement programs • Contribute to the leadership and direction of the Business Unit (BU) • Lead the operational contribution to proposal development and business development activities at a project level • Provide senior operational and strategic direction for Safety Project Leadership • Mentor, support and direct the functional team to develop robust patient engagement strategies • Identify knowledge gaps and develop plans to build skills across the business • Facilitate functional team metrics collection and case study creation • Provide expertise in Safety Project Leadership and project management best practices • Strive to ensure internal and external clients receive the required deliverables within stipulated timelines and budget Requirements: • Minimum 13+ years of pharmaceutical and/or CRO experience including but not limited to areas of focus in clinical operations, sales and decentralized clinical trials/direct to patient studies • 7-10 years of management experience, including direct project management or program oversight Benefits: • Excellent leadership and line management skills • Excellent knowledge of drug safety and the drug development process • Excellent knowledge of and ability to interpret and apply global safety regulations • Experience in data analysis, evaluation of safety data and the preparation of safety reports preferred • Excellent team / project leadership and delegation skills • Ability to train and mentor people • Excellent presentation skills • Excellent interpersonal skills • Excellent time management skills • Client focused approach to work • Experience with Pharmacovigilance related computing systems • Clinical Research or Pharmacovigilance knowledge /qualifications • Computer proficiency, ability to work with web-based applications and familiarity with the Windows operating system and Microsoft Office apps • Ability to comprehend various regulatory or client requests and be able to strategize a handling approach • Flexible attitude with respect to work assignments and new learnings • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail • Willingness to work in a matrix environment and to value the importance of teamwork