STEM Content Analyst - Market Access

4w1 month ago

Clarivate

Bengaluru, IN · Full-time · INR 600,000 – INR 900,000

About this role

Clarivate provides transparency in the position of brands, understanding of the market, and identifying opportunities and challenges across the US Healthcare Market. We deliver business-critical information regarding restrictions policies of payers for a wide variety of therapeutic indications.

We are looking for a STEM Content Analyst to join our Policy/Restrictions Content team in Bangalore. This is a clinically oriented role focusing on research, data entry, and analysis of restrictions policy data, requiring extreme accuracy and a high level of clinical knowledge.

You will accurately source, research, evaluate, interpret, and enter Payer restrictions information into the database using Gen AI for all therapeutic classes as assigned. You will collaborate with the Restrictions team to ensure consistency in data interpretation and assist in automation workflows pertaining to Restrictions Policy Research.

The Market Access Policy team works in close collaboration with stakeholders across Content Operations and the wider Life Science business. Our Policy team consists of colleagues based in India, the US, and Canada, offering a hybrid work environment with hours from 12 PM to 9 PM IST.

Requirements

Bachelor’s or Master’s degree in Pharmaceutical Science.
Minimum of 2 years of strong familiarity with Market Access/Managed Care data/PBM.
Advanced computer literacy and knowledge of Microsoft Office Suite.
Ability to understand and interpret clinical data.
Excellent oral and written communication skills.
Proven track record of working in a team environment.
Ability to adapt to ever-changing client and healthcare market demands.

Responsibilities

Accurately source, research, evaluate, interpret, and enter Payer restrictions information into the database using Gen AI for all therapeutic classes as assigned.
Collaborate with the Restrictions team to ensure consistency in interpretation of data.
Collect and appropriately store all supportive documentation for formulary and restrictions data.
Assist in Automation Workflow as it pertains to Restrictions Policy Research.
Assist in various Ad-Hoc Research Projects to meet Restrictions Deliverables for clients.