As a Portfolio Team Lead, you will play a crucial role in the success of our clinical trials. This position reports directly to the Portfolio Country Head and is responsible for overseeing the activities of Clinical Project Managers (CPMs) in their study-specific tasks.
The successful candidate will ensure that CPMs coordinate their activities across all CRAs working on the same trials/projects in collaboration with CRA Managers/FSP line managers. Key responsibilities include collaborating with the Leadership team to implement innovative practices and patient engagement tactics for advancing clinical trial planning, execution, and quality.
Key Responsibilities:
* Collaborate with the Leadership team to implement innovative practices and patient engagement tactics for advancing clinical trial planning, execution, and quality.
* Identify and lead innovative solutions to advance Project Management in the GDD portfolio in collaboration with Study & Site Operations country leadership.
* Support the Country Portfolio Head in implementing the global strategy within the country structure.
* Collaborate with SSO Feasibility Manager, SSO Site Partnership Manager, and others to develop opportunities that give GDD trials a competitive advantage.
* Ensure country study site selection, activation, enrolment, data flow, and timeline commitments are delivered as planned.
* Ensure adherence to clinical data standards, legislation, GCP, Ethical Committee, and SOP requirements.
* Manage the hiring, training, development, and retention of a team of Clinical Project Managers.
* Manage country study budgets and ensure study milestones are reached in a timely manner.
Essential Requirements:
* Scientific/healthcare degree and experience in clinical operations or project management.
* At least 8 years' experience in clinical research and/or project management with proven team management and leadership capabilities.
* Understanding of all aspects of clinical drug development, focusing on monitoring and trial execution.
* Thorough understanding of international drug development processes, standards, and regulations.
* Demonstrated negotiation and conflict resolution skills.
* Excellent project management skills with the ability to problem solve and mediate complex issues.
* Effective communication skills in a local/global matrixed environment.
* Fluency in both written and spoken English.
We are committed to building an inclusive work environment and diverse teams that reflect the communities we serve.
This role offers the opportunity to work in a dynamic and collaborative environment where you can make a significant impact on the success of our clinical trials.
If this role is not suitable but you wish to stay connected and learn more about career opportunities, visit our website to explore other job openings.