Who We Are

Escalent is an award-winning data analytics and advisory firm that helps clients understand human and market behaviors to navigate disruption. As catalysts of progress for more than 40 years, our strategies guide the world’s leading brands. We accelerate growth by creating a seamless flow between primary, secondary, syndicated, and internal business data, providing consulting and advisory services from insights through implementation. Based on a profound understanding of what drives human beings and markets, we identify actions that build brands, enhance customer experiences, inspire product innovation and boost business productivity. We listen, learn, question, discover, innovate, and deliver—for each other and our clients—to make the world work better for people.

Why Escalent? Once you join our team you will have the opportunity to...

• Access experts across industries for maximum learning opportunities including Weekly Knowledge Sharing Sessions, LinkedIn Learning, and more.
• Gain exposure to a rich variety of research techniques from knowledgeable professionals.
• Enjoy a remote first/hybrid work environment with a flexible schedule.
• Obtain insights into the needs and challenges of your clients—to learn how the world’s leading brands use research.
• Experience peace of mind working for a company with a commitment to conducting research ethically.
• Build lasting relationships with fun colleagues in a culture that values each person.

Key Objectives:

We are looking for a suitable candidate to support one of our Pharmaceutical clients. Primary objective is to assist the client in meeting their mandatory regulatory compliance requirements.

The role requires the candidate to have an eye for detail and communicate his/her thoughts in a structured manner.

Position Objectives and Expectations:

• Gather and integrate data from multiple sources, like medicinal product information report, licensing records
• Transcribe the product information into the client supported database(s) and tool(s)
• Perform accurate coding for the medicinal products, using the client approved standardized dictionary terminology (Medicinal Dictionary for Regulatory Activities)
• Adhere to business and compliance rules, as per pre-defined client SLAs (Service Level Agreements)
• Identify gaps based on client’s requirement and intervene when necessary to aid the group in resolving issues
• Always meet the deadline with the highest standard of quality
• Demonstrate high integrity, sense of urgency, ability to recognize time sensitivity
• Maintain confidentiality of all official information
• Operate within the agreed customer and Escalent SOPs (Standard Operating Procedures)

Personal Success Characteristics:

• Attention to detail
• Knowledge of Medical terms and terminology
• Solid time management skills
• Effectively cope up with the daily deadline requirements
• Ability to work in different shifts, if required (no night shifts)
• Professional approach to problem solving
• Excellent written and verbal communication
• Ability to maintain a professional demeanour under challenging situation

Previous Experience Requirements:

Preferred experience/specialization in Pharmacology or Drug Regulatory affair

Educational Requirements:

M. Pharma

Title:

Management Trainee

Location:

Noida/ WFH

Reports to:

Manager/ Director