Regulatory Affairs Job for Pharma Freshers at Accenture | Apply Now
Are you a fresher looking to start your career in the pharmaceutical industry? This Regulatory Affairs Job at Accenture is an excellent Pharma Freshers Job opportunity in Bengaluru. Join as a LifeScience Regulatory Services Associate and gain hands-on experience in regulatory operations, global submissions, and compliance within the life sciences domain.
- Job Title: LifeScience Regulatory Services Associate
- Job No.: AIOC-S01634595
- Location: Bengaluru
About the Company
Accenture is a leading multinational professional services company specializing in consulting, technology, and operations. Headquartered in Dublin, it operates in over 120 countries and employs more than 700,000 people worldwide. Accenture helps organizations improve performance and drive digital transformation through services like cloud computing, artificial intelligence, cybersecurity, and data analytics. It serves a wide range of industries, including healthcare, pharmaceuticals, banking, and retail, and is known for working with top global clients.
Job Description
- Aligned with the Life Sciences R&D vertical, supporting end-to-end services
- Covers research labs, clinical trials, regulatory services, pharmacovigilance, and patient solutions
- Part of sub-offerings: Clinical, Pharmacovigilance & Regulatory
- Supports global biopharma companies in improving patient outcomes
- Focus on combining scientific expertise with patient insights
Regulatory Services Responsibilities:
- Ensure compliance with laws and regulatory requirements
- Guide regulatory frameworks and standards
- Prepare and submit regulatory documentation and reports
- Stay updated with regulatory changes and guidelines
- Conduct compliance audits
Key Tasks:
- Coordinate documentation for global regulatory filings
- Manage electronic submissions (eCTD)
- Handle:
- Original application filings
- Life Cycle Management (LCM) submissions (CMC, Ad-promos, amendments)
- Annual reports
- SPL submissions
Key Responsibilities
- In this role, you are required to solve routine problems, largely through precedent and referral to general guidelines
- Your expected interactions are within your own team and with your direct supervisor
- You will be provided with a detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments
- The decisions that you make will impact your own work
- You will be an individual contributor as part of a team, with a predetermined, focused scope of work
- Please note that this role may require you to work in rotational shifts
Qualification
- Bachelor of Pharmacy/Master of Pharmacy
- Skill required: Regulatory Services – Life Sciences Regulatory Operations
- Designation: LifeScience Regulatory Svs Associate
- Years of Experience: 0 to 3 years
- Language – Ability: English(International) – Proficient
