MSc, B Pharm, M Pharm Fresher Hiring as Associate STEM Content Analyst Chemistry | Clarivate

Clarivate Hiring Associate STEM Content Analyst in Hyderabad – B.Pharm, M.Pharm & MSc Freshers Eligible

Clarivate has announced a hiring opportunity for the role of Associate STEM Content Analyst within its Clinical Studies team located in Hyderabad, Telangana. The position is offered in a hybrid work model and is open to freshers or candidates with up to six months of experience in clinical research analysis or scientific data review.

This role sits within the Life Sciences and Healthcare division and supports Clarivate’s globally recognized intelligence platforms such as Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. These platforms are widely used by pharmaceutical companies, biotechnology firms, and research organizations to track drug pipelines, analyze clinical trials, and support strategic decisions in drug development.

For graduates in pharmacy and life sciences, this opening provides a valuable entry point into the growing field of clinical research intelligence, pharmaceutical data analysis, and drug development research support. Professionals joining this team will contribute to maintaining accurate clinical trial databases used by global pharmaceutical innovators.

Company Overview

Clarivate is a global analytics and insights company that provides trusted data, research tools, and technology solutions to organizations across life sciences, healthcare, academia, and intellectual property sectors.

The company is best known for its powerful information platforms that help researchers, pharmaceutical companies, and academic institutions make evidence-based decisions. Clarivate products support activities such as drug discovery, clinical research, regulatory planning, and scientific publishing.

Within the life sciences industry, Clarivate plays a major role in delivering drug pipeline intelligence, clinical trial analytics, and scientific research insights. Pharmaceutical companies rely on Clarivate’s data platforms to track emerging therapies, analyze competitive landscapes, and evaluate clinical development strategies.

The Hyderabad office supports several global research and analytics operations, particularly in life sciences data management and clinical intelligence services. Professionals working in these teams contribute directly to improving the availability and accuracy of pharmaceutical research data used worldwide.

By joining Clarivate, candidates gain exposure to global clinical trial information, drug discovery programs, and pharmaceutical innovation trends while working in a collaborative and knowledge-driven environment.

Job Role & Responsibilities

The Associate STEM Content Analyst will work as part of the Clinical Studies team responsible for maintaining and updating clinical trial intelligence databases used by global pharmaceutical organizations.

The role involves reviewing scientific information from various sources, analyzing clinical trial data, and ensuring accurate records within Clarivate’s research platforms.

Key responsibilities include:

• Monitoring multiple scientific and clinical information sources such as conferences, trial registries, press releases, and research publications
• Collecting, reviewing, and validating clinical trial information related to pharmaceutical drug development
• Updating clinical study records within the Cortellis intelligence databases
• Cross-referencing information from multiple sources to ensure accuracy and completeness of clinical trial data
• Maintaining up-to-date records of drug development programs and clinical study progress
• Interpreting complex clinical trial information and converting it into structured database entries
• Meeting weekly productivity and data quality targets set by the clinical research team
• Ensuring data quality and compliance with internal editorial standards
• Identifying discrepancies in clinical trial information and resolving them through research and analysis

This role requires strong attention to detail and analytical thinking, as the accuracy of the clinical database directly impacts research decisions made by pharmaceutical companies.

Eligibility / Qualifications

Candidates applying for the Associate STEM Content Analyst role should have a strong academic background in life sciences or pharmaceutical sciences and a genuine interest in clinical research and drug development.

Educational Qualification

Candidates should possess one of the following degrees from a recognized university:

B.Pharm, M.Pharm, MSc Biotechnology, MSc Microbiology, MSc Life Sciences, MSc Biochemistry.

These academic programs provide foundational knowledge in pharmacology, drug development, microbiology, biotechnology, and clinical research processes that are essential for analyzing clinical study data.

Experience

The position is suitable for freshers or candidates with up to six months of relevant experience in clinical research analysis, scientific content review, or pharmaceutical data research.

Experience in secondary research related to clinical trials or pharmaceutical information will be considered an advantage but is not mandatory.

Required Skills

Candidates should demonstrate the following competencies:

• Strong understanding of clinical trials, drug pipelines, and pharmaceutical development phases
• Ability to interpret complex clinical study data and research information
• Excellent written and verbal communication skills in English
• Strong analytical and problem-solving abilities
• Ability to conduct research across multiple scientific information sources
• Attention to detail when reviewing and updating clinical research data
• Ability to work within defined productivity targets and quality standards

Candidates who are curious, research-oriented, and comfortable working with large volumes of scientific information are likely to perform well in this role.

Location & Salary

Location: Hyderabad, Telangana, India

Work Model: Hybrid (Monday to Friday)

Working Hours: 9:00 AM – 6:00 PM

Application Process

Interested candidates can apply through the official Clarivate careers portal using the link below:

Apply Online:

https://careers.clarivate.com/job/CLACLAGBJREQ134953EXTERNALENGB/Associate-STEM-Content-Analyst

Applicants may be contacted by the Clarivate recruitment team for further evaluation, which may include assessments of analytical skills, understanding of clinical research concepts, and communication ability.

Candidates are advised to keep their updated resumes ready and highlight any coursework or project experience related to clinical trials, drug development, or pharmaceutical research.

Frequently Asked Questions (FAQs)

Who can apply for the Clarivate Associate STEM Content Analyst role?

Candidates with B.Pharm, M.Pharm, or MSc degrees in Biotechnology, Microbiology, Life Sciences, or Biochemistry can apply for this role.

Are freshers eligible for this position?

Yes. Fresh graduates or candidates with up to six months of experience in clinical research analysis or scientific research support are eligible.

What does a STEM Content Analyst do in the pharmaceutical industry?

They collect, analyze, and maintain clinical trial data, drug pipeline information, and scientific research updates used by pharmaceutical companies for strategic decision-making.

Where is the job located?

The role is based in Hyderabad, Telangana, with a hybrid working model.

What career growth opportunities exist in clinical intelligence roles?

Professionals can grow into roles such as Clinical Research Analyst, Drug Pipeline Intelligence Specialist, Medical Information Analyst, or Life Sciences Research Consultant.

Summary

Company	Clarivate
Vacancies	Associate STEM Content Analyst
Required Education	B.Pharm, M.Pharm, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Life Sciences
Experience	Freshers or Up to 6 Months Experience in Clinical Research / Data Analysis

Tagged as: Pharma Jobs in Hyderabad