Chief Operations Officer

10 - 31 years

9 - 12 Lacs

Posted:4 days ago| Platform: Apna logo

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Work Mode

On-site

Job Type

Full Time

Job Description

A pharma project manager's job involves leading drug development projects from concept to market by planning, executing, and monitoring all project phases while managing budgets, timelines, and cross-functional teams. They are the key point of contact, communicating with stakeholders like regulatory bodies, scientists, and management to ensure project goals are met and risks are controlled. This requires a deep understanding of pharmaceutical processes and regulatory requirements to successfully bring new life-saving medications to patients.   Key Responsibilities ·        Project Planning & Execution:  Developing detailed project plans, identifying tasks, timelines, and resource allocation for new drug development or other pharmaceutical initiatives.  ·        Budget & Resource Management:  Overseeing project budgets, ensuring projects remain on schedule and within financial constraints, and allocating resources effectively.  ·        Team Leadership:  Assembling and leading multi-disciplinary project teams, including scientists, researchers, regulatory experts, and other specialists.  ·        Risk Management:  Proactively identifying, assessing, and mitigating project-related risks to prevent delays and ensure successful outcomes.  ·        Quality & Regulatory Compliance:  Ensuring that all project activities adhere to industry standards, including GMP (Good Manufacturing Practices), and all applicable regulatory requirements.  ·        Monitoring & Reporting:  Tracking project progress, monitoring key performance indicators, and providing regular status reports and updates to management.  ·        Problem-Solving:  Addressing unexpected challenges and making decisions to keep the project on track towards its objectives.  Essential Skills & Knowledge   ·        Pharmaceutical Knowledge:  A strong understanding of the drug development process, from research and clinical trials to regulatory submission and market launch.  ·        Regulatory Expertise:  Familiarity with the complex regulatory landscape governing pharmaceutical products.  ·        Leadership & Communication:  Strong leadership to motivate teams and excellent communication skills to effectively interact with diverse stakeholders.  ·        Technical Skills:  Ability to use project management software and manage complex charts for long-term projects.  ·        Analytical Skills:  Capable of analyzing data, identifying issues, and developing cost-effective solutions.   

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