Key Responsibilities:

• Lead the clinical trial team in the delivery of multiple medium to complex global studies, promoting a learning and sharing environment, consistent performance, and operational excellence.
• Create effective CTT dynamics and achieve performance, priorities, and communication in close collaboration with CTT sub-team leaders.
• Guide planning and decision making at the study level, ensuring assigned clinical studies are delivered per the Operational Execution Plan (OEP) and clinical study protocol.
• Foster an agile culture within assigned studies, working to achieve sprint goals and cycles, thereby maximizing collaboration and minimizing dependencies.
• Oversees study recruitment and responsible for activating mitigation strategies.
• Achieves excellence in study operations and management through process improvement.

Essential Requirements:

• Bachelor’s degree in life sciences/healthcare or clinically relevant degree. An advanced degree is a plus.
• At least 4 years of recent involvement in clinical research or drug development, spanning Phases I through IV clinical activities.
• ≥ 3 years of recent experience in conducting clinical studies (e.g. planning, executing, reporting and publishing) in a global/matrix environment within the pharmaceutical industry or a contract research organization.
• Experience managing people globally within a complex matrix environment is preferred.
• Proven abilities in negotiation and conflict resolution, strategic thinking, strong analytical, and problem-solving skills.
• Experience in developing effective working relationships with internal and external stakeholders
• Excellent communication and presentation skills (both oral and written), with the ability to communicate across all levels.