Job Description

About AstraZeneca
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the worlds most serious diseases. But were more than one of the worlds leading pharmaceutical companies.
Regulatory Affairs Sr Manager (Clinical Trials)
Reports to Director - Regulatory Affairs
Position purpose

• Coordinate with key stakeholders (local regulatory authority, local MC and Global Regulatory Affairs etc.) to achieve rapid/high-quality submissions and approvals related to Clinical Trials
• Prepare/review high-quality regulatory dossiers for GCT/Phase IV studies submissions
• Monitor the Clinical Trial approval process and promptly report whenever necessary
• Life cycle management of Clinical trials
• Adequate support in SEC preparations
• Collates, communicates, prepares/reviews to Health authorities queries
• Participate in Regulatory meetings with Health authorities as well as in internal meetings for Regulatory issues/follow-up.
• Performs periodic reviews of the archival
• Liaise with several government agencies to procure timely deliverables

Minimum requirements Qualification: M.Pharm/B.Pharm/ 6-10 yrs Experience in India Regulatory function, knowledge of dossier compilation. He/ she should be conversant with Indian regulations.
Key Result Areas/ outputs xc2xb7

• Adherence to AZ and industry codes of conduct, ethics and good regulatory practices
• Ensure that all licensing for assigned products is complete in accordance with relevant norms
• Develop and implement action regulatory plans for allocated products to achieve requisite approvals rapidly and facilitate rapid launch
• Maintain the awareness of, and shape the regulatory environment relevant to the assigned products portfolio
• Competitive Intelligence and analysis

Adherence to AZ and industry codes of conduct, ethics and good regulatory practices
xc2xb7 Align with the values and vision of AZ
xc2xb7 Ensure compliance with Local legislation, Global regulatory policies, AZ code of
conduct, Corporate Governance and Audit requirement
xc2xb7 Ensure that company confidentiality is maintained (i.e. intellectual property, product
information and strategic information)
xc2xb7 Disclose potential breach of codes or conducts
Key Result Areas/outputs Activities

• Ensure that all licensing for assigned products is complete in accordance with relevant norms
• Monitor status of product licenses
• Project manage changes in product licenses and coordinate with other changes, planned and in progress
• Maintain complete documentation records
• Communicate changes to licenses status promptly
• Develop and implement action regulatory plans for allocated products to
• achieve requisite approvals rapidly and facilitate rapid launch
• Maintain detailed knowledge of critical aspects of products: commercial strategies, content of the dossiers, regulatory intelligence, regulatory timelines and supply strategy
• Ensure that local regulatory strategies are consistent with global product strategies and local priorities
• Develop regulatory plan in conjunction with key stakeholders and ensure allocation of adequate resources and deliver plans on time
• Track status and take prompt corrective measures whenever necessary to ensure rapid approval and launch
• Provide Leadership and direction within project teams
• Strive to ensure high levels of performance and achievements.
• Take decision and accountability for actions.
• Build commitment within the team.
• Enhance positive attitudes and mindset.
• Demonstrate confidence and conviction.
• Challenge status quo for continuous improvement. xc2xb7 Help build an open and trusting atmosphere.
• Assist in Issue Management
• Provide detailed information of regulatory status of affected products
• Undertake assigned follow-up action where necessary
• Maintain the awareness of, and shape the regulatory environment relevant to the assigned products
• Portfolio Interact with relevant regulatory authorities on a regular basis to facilitate the process of obtaining necessary approvals / permissions
• Monitor and understand the impact of external changes in the regulatory and political environment that will impact on the assigned products
• Communicate the impact of changes to key stakeholders.
• Influence key external stakeholders, in line with codes of conduct, to improve regulatory outcomes
• Develop excellent relationships and partnerships with Regulatory Authorities
• Competitive Intelligence and Analysis
• Monitor the global pipelines of competing pharmaceutical companies
• Analyse gathered information for its impact on AstraZeneca proposed pipelines
• Provide scenario with options and a risk benefit analysis for AstraZeneca going forward

Why AstraZeneca?
At AstraZeneca were dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. Theres no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. Were on an exciting journey to pioneer the future of healthcare.
Date Posted 26-May-2025
Closing Date 29-Jun-2025
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.