Associate STEM Content Analyst - JREQ131835
Location: Tamil Nadu, India (Hybrid work model)
Department: Life Sciences & Healthcare
Job Type: Permanent contract
About the Role
We are seeking an Associate STEM Content Analyst to join our Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence team. In this role, you will analyze and update clinical trial reports from various sources, ensuring that the information is accurate and up-to-date. You will also collaborate with the team to meet targets, maintain consistent quality standards, and contribute to the overall success of the team.
Responsibilities
Actively seek out information about clinical trials, analyze, cross-reference, and update records with the latest information from sources such as company websites, presentations, conferences, press releases, clinical trial repositories, and other internet sources.
Record and track performance against targets to ensure the team achieves its objectives.
Take an active role within the team to ensure targets are met consistently.
Stay informed of developments in clinical trials and related technology areas.
Maintain consistent quality standards while managing your time effectively.
Adapt to process changes and maintain a flexible approach.
Identify personal technology training and development needs and pursue ongoing growth.
Undertake additional duties as requested by your line manager/director, both on a permanent and temporary basis.
Qualifications & Experience
Required:
Education: BPharm/MPharm/MSc in Biotechnology, Microbiology, Life Sciences, or related field.
At least 2 years of experience in analyzing and updating clinical reports.
In-depth knowledge of clinical trials, pharmaceutical drug pipelines, drug development, and clinical phases.
Excellent written and verbal communication skills in English.
Desired:
Experience in secondary research related to clinical information.
Ability to analyze content in-depth and generate meaningful insights.
About the Team
You will be part of a team working on Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence, with a group size of around 20 members, including Content Specialists, Senior Content Analysts, and Content Analysts. The team culture emphasizes collaboration, accuracy, and continuous improvement.
Work Hours
Full-Time: 8 hours per day
Hybrid Work: Monday to Friday
Equal Employment Opportunity
Clarivate is committed to providing equal employment opportunities to all individuals, regardless of their background. We adhere to all applicable laws and regulations governing non-discrimination in employment.
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