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Associate STEM Content Analyst

Associate STEM Content Analyst

Clarivate

0 - 3 years

3 - 5 Lacs

hyderabad

Posted:1 day ago| Platform:

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Skills Required

python financial analysis time management ai process improvement research sql microsoft office ai tools secondary research clinical trials competitive analysis communication skills

Work Mode

Work from Office

Job Type

Full Time

Job Description

We are looking for an Analyst to join our CDDI Drugs team in Hyderabad, India. This is an amazing opportunity to work on drug development research (including both primary and secondary research), competitive analysis, company communications, presentations, pipeline and clinical trial analysis, financial analysis, and produce comprehensive drug development data. The team consists of around 6 colleagues spread across India and Spain, reporting to the same team manager. We have a great skill set in the drug development industry, from drugs patents to market access, and we would love to speak with you if you have skills or interest for the same.

About You experience, education, skills, and accomplishments

Freshers or 6 months of relevant experience in
M Pharm, BPharm or D Pharm degree
Knowledge in content analysis & editing
Good interpersonal skills and communication skills (written and oral)
A good teamplayer with the ability to work on own initiative
Effective time management
Highly motivated with a strong work ethic and ability to thrive in a fast-paced environment
Adhere to SOP and Policies
Ability to work well under challenging situations and meet deadlines
Proficiency with Microsoft Office products (Word, Excel, and PowerPoint)

It would be great if you also had . . .

Proficiency in using AI tools in your day-to-day work

Knowledge of SQL/ Python

What will you be doing in this role

Analyse drug-based references (clinical trials, company/research institution press releases and websites, regulatory information from FDA, EMA)
Identify new drugs and/or drug updates (new drug names, development phase, target disease, formulation, organizations involved in drug development)
Able to understand and process reference information, summarize and edit it without grammatical and conceptual errors
To do comprehensive search for finding drug related references online
Should meet weekly production volume and quality targets consistently; achieve KPI metrics
Actively participate with the team and work towards process improvement
Collaborate with ROW & Cross BU groups on demand
To be flexible and adaptable towards process change
To complete the tasks demanded by your line manager / director on a permanent or temporary basis.

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Associate STEM Content Analyst