Key skills
Oncology clinical trialsClinical trial conductRegulatory requirementsTherapeutic areasMS OfficeProject management toolsProject managementGCPLeadershipProject ManagementCommunicationCollaborationNegotiation
About this role
IQVIA is a full-service CRO with over 25 years of experience, dedicated to serving biotech sponsors. The Senior Project Manager will lead complex, multi-regional clinical studies in Oncology, ensuring operational excellence and strong client relationships.
Responsibilities:
- Lead bid defense presentations and contribute to study strategy development
- Develop and implement integrated study management plans
- Oversee planning and execution of medium to large, multi-regional clinical studies, ensuring speed, quality, and cost optimization
- Serve as the primary point of contact for clients, fostering strong relationships and customer satisfaction
- Build and lead cross-functional teams, driving collaboration and milestone achievement
- Monitor project progress, manage risks, and resolve issues proactively
- Ensure compliance with ICH GCP, local regulations, and company processes
- Manage project financials, including forecasting, scope changes, and revenue acceleration opportunities
- Mentor and support team members, promoting continuous improvement and knowledge sharing
Requirements:
- Bachelor's degree in Life Sciences or related field
- 7+ years of clinical research experience, including 4+ years in project management
- Strong knowledge of clinical trial conduct, regulatory requirements, and therapeutic areas
- Excellent leadership, communication, and negotiation skills
- Proven ability to manage complex projects across geographies and functions
- Proficiency in MS Office and project management tools