When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will perk a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Lead end-to-end signal management activities including detection, validation, evaluation, tracking, and closure
Perform and oversee qualitative and quantitative signal analysis across clinical, post-marketing, literature, and regulatory data sources
Ensure compliance with global pharmacovigilance regulations and client-specific processes
Provide oversight and/or author aggregate safety reports (Periodic Benefit-Risk Evaluation Report (PBRERs), Development Safety Update Reports (DSURs), Risk Management Plans (RMPs), and allied documents)
Guide development of Corporate Social Responsibility (CSR) narratives and safety assessments, ensuring scientific rigor and regulatory compliance
Ensure effective integration of signal outputs into aggregate reporting and risk management strategies
Oversee delivery across signal management and aggregate writing programs
Manage timelines, resources, budgets, and risks to ensure high-quality, on-time delivery
Drive operational excellence, efficiency, and continuous process improvement
Managerial Responsibilities
Provide overall leadership and strategic direction to teams, ensuring alignment with organizational goals and client expectations
Oversee end-to-end delivery, ensuring quality, timeliness, and efficiency across projects
Manage resource planning, workload distribution, and budget considerations to optimize productivity
Drive performance management, coaching, and deve
📌 Senior Manager, Medical Writing Services Hyderabad (India)
🏢 Parexel
📍 India