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Work as Senior Regulatory Affairs Associate at PAREXEL


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Work as Senior Regulatory Affairs Associate at PAREXEL

PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.

Post : Senior Regulatory Affairs Associate

Candidate Profile
• Around 4-8 years of relevant experience in handling of pre and post approval life cycle management of  drug products (small molecules as well as biologics) in various markets.
• Good understanding of regulatory framework, including regional trends, for various types of applications and procedures
• Contribute to preparation (including authoring where relevant) and delivery of simple, and with experience, increasingly more complex regulatory maintenance submissions from either a global and/or regional perspective.
• Working knowledge of EU/US regulatory procedures including post approval requirements. Knowledge of ROW markets regulatory legislations would be an added advantage
• Experience in handling CMC related health authority queries
• Good understanding of regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions as well as knowledge of global pharmaceutical legislation and guidance specifically linked to regulatory CMC aspects in the ICH countries.
• Preparation and review of Marketing Authorization Applications & Variations for various types of medicinal products (Orals & Parenterals) for filing in EU through different types of procedures (DCP/MRP/National Procedures).

• Preparation of documentation for different types of Variation procedures like Super grouping,
• Grouping and Work-sharing to the Marketing Authorizations.
• Regulatory review of DMFs, batch records, specifications, and stability data to ensure their compliance with the regulatory requirements.
• Providing regulatory impact assessment for change proposals and identification of required documentation for EU submissions
• Liaise closely with cross-functional members with aligned product responsibilities.
• Execute and maintain submission delivery plans, submission content plans, and proactively provide status updates to designated stakeholders.
• To prepare, review and submit safety variations to Health Authorities and perform post Approval CMC related updates.
• Working experience in Regulatory Information Management Systems like Veeva Vault.
• Strong communications skills and ability to guide and mentor team members.

Additional Information
Location : Mumbai, Hyderabad
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Regulatory
End Date : 31st May 2024

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