Key Responsibilities:

• Provide clinical strategic and tactical leadership for country clinical development and research programs or trials.
• Gather, inform, and act on clinical, medical or scientific insights to optimize clinical trial implementation.
• Drive the identification and involvement of qualified investigators and overcome clinical recruitment hurdles.
• Ensure adherence to safety standards and clinical data quality in the country.
• Collaborate with country functions to ensure successful trial start-up, timely recruitment, and mitigation of potential delays.
• Provide clinical or medical expertise during interactions with external experts and regulatory authorities.
• Support planning, implementation, and follow-up of scientific, clinical or medical components of regulatory inspections and internal audits.

Essential Requirements:

• Scientific degree (M.D., Ph.D.) with subspecialty training desirable.
• Minimum 2-5 years of clinical development experience in the pharmaceutical industry or clinical practice.
• Strong understanding of the overall clinical development process and ICH/GCP principles.
• Ability to manage studies from a scientific, medical or clinical perspective and solve complex issues.
• Effective leadership and communication skills to motivate cross-functional teams.
• Willingness to travel as when needed.

Skills:

• Clinical Monitoring.
• Clinical Research.
• Clinical Trial Protocol.
• Clinical Trials.
• Decision Making Skills.
• Drug Development.
• Health Sciences.
• Lifesciences.
• Regulatory Compliance.

Languages :

• English.