Indero
Published on: 14th July 2025
Position: Regulatory Documents Assistant
Experience: 0–1 Year
Qualification: B.Pharm, M.Pharm
Hiring Type: Apply Online (Email/Web Application)
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🏢 About the Company
Indero is a renowned Contract Research Organization (CRO) focused on clinical trials in dermatology and rheumatology. Since 2000, Indero has maintained a reputation for excellence, operating across Montreal, North America, and Europe. The company is committed to delivering high-quality, regulatory-compliant research services and continues to grow its global presence, including operations in India.
📋 Position: Regulatory Documents Assistant
As a Regulatory Documents Assistant, your key responsibilities will include:
Setting up and maintaining electronic and paper Trial Master Files (TMFs)
Reviewing documents to ensure compliance with ICH-GCP and SOPs
Supporting eTMF setup, quality reviews, and metadata tracking
Ensuring accuracy of site-level regulatory documents
Collaborating with CRAs, project teams, and investigative sites
Providing administrative support such as material shipment coordination and tracking
✅ Skills Required
Proficiency in Microsoft Word & Excel
Strong organizational and multitasking skills
High attention to detail and ability to meet deadlines
📝 Eligibility & Application
Qualification: B.Pharm or M.Pharm
Experience: 0–1 year
Location: Delhi
Documents Required:
Updated Resume
Educational Certificates
Government ID