Job Description

Roles and Responsibilities Manage program management activities, including planning, execution, monitoring, and controlling of programs. Coordinate with cross-functional teams to ensure effective communication and collaboration. Develop and maintain project plans, timelines, budgets, and resource allocation plans. Ensure compliance with regulatory requirements and company policies. Identify potential risks and develop mitigation strategies. Desired Candidate Profile 12-18 years of experience in pharmaceutical industry or related field (Clinical Trials). Master degree from a recognized institution. Strong understanding of regulations (e.g., GCP, USFDA, EU) and ICH guidelines. Excellent communication skills in English; ability to work effectively with international stakeholders. Proficiency in MS Office applications (Word, Excel).