Genpact (NYSE: G) is a global professional services and solutions firm delivering outcomes that shape the future. Our 125,000 people across 30 countries are driven by our innate curiosity, entrepreneurial agility, and desire to create lasting value for clients. Powered by our purpose – the relentless pursuit of a world that works better for people – we serve and transform leading enterprises, including the Fortune Global 500, with our deep business and industry knowledge, digital operations services, and expertise in data, technology, and AI.

Inviting applications for the role of Manager, Regulatory Affairs
We are inviting applications for the role of Manager, Regulatory affairs.

Responsibilities:
• Develop and support clinical study/submission strategy for lifesaving therapeutic products in development and through life cycle management considering all relevant guidance, commercial needs, and company objectives.
• Develop strategic direction and provide leadership for all interactions related to clinical/medical studies with FDA/EMA/global regulatory authorities.
• Lead new dossier submissions to global and/or FDA (IND, BLA, NDA, and supplements) utilizing internal and external resources
• Maintain an up-to-date knowledge of medical terminologies, complex scientific concepts (like cell gene therapy)
• Able to author Module 4 5 components for FDA – BLA EMA new submissions for biologics, preferably in cell gene therapy
• Conduct literature reviews to support clinical development activities and regulatory submissions
• Writing clinical documents (e.g. new INDs, briefing book content, BT Designation request, Priority Review Requests, ODD); reviewing core documents to support IND/BLA/NDA, in conjunction with EUL or GRL as needed.
• Foster positive relationships with FDA.
• Build and maintain a strong, collaborative relationship with all key stakeholders including Commercial, Medical Affairs, Promotion Compliance, Global Development, and other functions key to the success of product development.
• Interact routinely and will develop a strong team environment with colleagues throughout GRS.
• Ability to lead client meetings and managing project governance.
• Work with cross-functional teams to track and follow up outstanding documentation, coordinate on project status reporting to stakeholders using different communication channels.
• Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills.
• Demonstrated understanding of related fields
• Demonstrated ability to generate innovative solutions to problems and effectively collaborate with and communicate to key stakeholders.
• Demonstrated flexibility in responding to changing priorities, multi-tasking and dealing with unexpected events.
• Demonstrated effective leadership, communication, and interpersonal skills.
• Strong ability to work successfully in a matrix environment and to lead teams successfully toward drug approvals.
• Significant experience in clinical writing
• Expert understanding of policy, laws, regulations, and guidelines as they apply to U.S. FDA EMA for drug development and approval.
• Expert understanding of drug development process and understanding of scientific content and complexities related to a project in life-saving therapeutic drugs.
• Direct experience in developing strategy and leading teams through interactions with FDA/EMA.
• Extensive experience in initiating and conducting successful interactions within FDA/EMA.
• Communicates opinions, facts and thoughts with clarity, transparency, and honesty.
• Demonstrates ownership of results within (and beyond) area of responsibility.
• Sets clear and high expectations and holds self and others accountable for decisions and results achieved.
• Looks for opportunities for continuous improvement.
Qualifications we seek in you
Minimum Qualifications / Skills
• Ph.D., M.D., PharmD., MS or commensurate experience

Genpact is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, religion or belief, sex, age, national origin, citizenship status, marital status, military/veteran status, genetic information, sexual orientation, gender identity, physical or mental disability or any other characteristic protected by applicable laws. Genpact is committed to creating a dynamic work environment that values diversity and inclusion, respect and integrity, customer focus, and innovation. Get to know us at genpact.com and on LinkedIn, X, YouTube, and Facebook.
Furthermore, please do note that Genpact does not charge fees to process job applications and applicants are not required to pay to participate in our hiring process in any other way. Examples of such scams include purchasing a 'starter kit,' paying to apply, or purchasing equipment or training.