B Pharm, M Pharm, or D Pharm Fresher Hiring | Associate STEM Content Analyst | Clarivate
- Clarivate Hiring: Associate STEM Content Analyst for Freshers
- Job Overview
- Key Responsibilities
- Qualifications and Requirements
- About Cortellis Drug Discovery Intelligence (CDDI)
- About the Team
- Location and Work Model
- How to Apply
- Apply Here
Clarivate Hiring: Associate STEM Content Analyst for Freshers
Are you a fresh graduate with a degree in B Pharm, M Pharm, or D Pharm and looking to kickstart your career in pharmacology and drug discovery? Clarivate is hiring an Associate STEM Content Analyst for its Experimental Pharmacology & Models team, with opportunities available in Chennai and Hyderabad. This is a great opportunity for freshers
Job Overview
As an Associate STEM Content Analyst, you will play a critical role in analyzing and updating pharmacological activities and data from various sources such as patents, journals, posters, and conference materials. Working within Clarivate’s innovative Cortellis Drug Discovery Intelligence platform, you will help provide essential biological, chemical, and pharmacological data that benefits scientists and researchers across the globe.
This is a hybrid position, giving you the flexibility to work from both the office and home, and is full-time with working hours from 9:00 AM to 6:00 PM IST.
Key Responsibilities
As an Associate STEM Content Analyst, your primary responsibilities will include:
- To review/analyze and update the Pharmacological Activities and to update the internal core database (CMS) according to the guidelines proposed.
- To review/analyze and update IN VITRO, IN VIVO and EX VIVO study from patents, references, posters, and conferences in CMS
- Pharmacological parameters and units measured, materials and the methods used in the respective activities from patents, references, posters, and conferences
- Pharmacological details of the drug including the animal model, dose regime, end point measurements and duration of the drug
- Achieve production volume and quality targets
- Recording of performance against target
- Taking an active role within the team to ensure targets are met
- Maintain awareness of current developments in own technology areas
- Achieve and maintain consistent quality standards, Effective personal planning, and time management
- Maintain a flexible and adaptable approach towards process change
- To take responsibility for identifying technology training and developmental needs for yourself on an on-going basis
- To make positive efforts to promote personal safety and that of others by taking reasonable care at work, by carrying out the requirements of the law or following recognized codes of practice provided or advised by management to ensure safe working practices
- To undertake any other reasonable duties as requested by your line manager / director on a permanent or temporary basis.
Qualifications and Requirements
To be eligible for the Associate STEM Content Analyst role, you should have the following qualifications:
- Educational Background: A degree in B Pharm, M Pharm, or D Pharm is required.
- Experience: Freshers or those with 0-1 year of experience in pharmacology content analysis are welcome to apply.
- Skills: Basic knowledge of pharmacology, drug development processes, and data analysis is essential. Familiarity with content management systems is a plus.
About Cortellis Drug Discovery Intelligence (CDDI)
Clarivate’s Cortellis Drug Discovery Intelligence is a cutting-edge platform designed to streamline pharmaceutical research. It harmonizes and integrates essential biological, chemical, and pharmacological data into one single source. The data provided through CDDI helps scientists research therapeutic drugs, experimental models, and the treatment of human diseases more efficiently.
About the Team
You will be joining the Experimental Pharmacology & Models team, which is responsible for analyzing journals, patents, and meeting abstracts. The team provides detailed pharmacological content for use within the CDDI platform, which is relied upon by pharmaceutical scientists and researchers worldwide.
Location and Work Model
- Location: Chennai/Hyderabad
- Work Model: Hybrid (Remote + In-Office)
- Hours: 40 hours per week, 9:00 AM – 6:00 PM IST
How to Apply
If you’re ready to start your career in pharmacology content analysis with Clarivate, apply today! Visit the link below to submit your application:
