Clarivate Hiring Associate STEM Content Analyst
- Clarivate Hiring Associate STEM Content Analyst | BPharm, MSc Biotechnology | Hyderabad Hybrid
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Eligibility & Qualifications
- Educational Background
- Experience & Skills
- Location & Employment Details
- Application Process
- Frequently Asked Questions (FAQs)
- 1. Is this role open to freshers?
- 2. Is prior clinical research experience mandatory?
- 3. What databases will the candidate work on?
- 4. Is the position fully remote?
- 5. What skills are critical for success?
- Summary Table
Clarivate Hiring Associate STEM Content Analyst | BPharm, MSc Biotechnology | Hyderabad Hybrid
Clarivate is hiring for the position of Associate STEM Content Analyst in the Life Sciences & Healthcare division at Hyderabad, Telangana. This is a hybrid, full-time opportunity within the Clinical Studies team, supporting Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence platforms. The role is open to freshers and candidates with up to 6 months of experience in analyzing and updating clinical reports.
If you are a B.Pharm, M.Pharm, or MSc graduate with strong knowledge of clinical trials, drug development phases, and pharmaceutical pipelines, this role offers a structured entry into clinical research intelligence, secondary research analysis, and healthcare data management within a global information solutions company.
Company Overview
entity[“organization”,”Clarivate”,”global information services company”] is a leading global provider of trusted insights and analytics across life sciences, healthcare, intellectual property, and academia. Its Cortellis platforms are widely used by pharmaceutical and biotechnology companies for clinical trial intelligence, drug discovery tracking, competitive landscape assessment, and regulatory research.
Through advanced data curation, scientific analysis, and structured healthcare intelligence solutions, Clarivate enables organizations to make informed strategic decisions in drug development, regulatory planning, and commercialization. The company operates globally and supports innovation by delivering accurate, timely, and research-driven content to industry stakeholders.
Working at Clarivate provides exposure to global pharmaceutical R&D data, competitive drug intelligence systems, and real-world clinical trial tracking platforms.
Job Role & Responsibilities
The Associate STEM Content Analyst will be part of the Clinical Studies team responsible for maintaining and updating structured clinical trial records within Clarivate’s Cortellis databases. The role involves detailed secondary research, cross-referencing scientific data, and ensuring high data accuracy standards.
Core Responsibilities
- Actively search for clinical study information from multiple sources including trial registries, scientific conferences, press releases, and regulatory announcements.
- Analyze, validate, and cross-reference new or updated clinical trial data.
- Update clinical records within the Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence platforms.
- Ensure database accuracy, completeness, and consistency.
- Interpret complex trial data including drug development stages and pipeline updates.
- Meet weekly productivity targets while maintaining quality benchmarks.
- Apply strong analytical thinking to identify discrepancies and resolve data issues.
- Collaborate with team members to maintain high editorial and scientific standards.
This position requires careful data handling, scientific understanding, and structured documentation practices.
Eligibility & Qualifications
Educational Background
Candidates must hold a degree in Life Sciences or Pharmacy.
Eligible qualifications include:
B.Pharm, M.Pharm, MSc Biotechnology, MSc Microbiology, MSc Life Sciences, BSc Biotechnology, BSc Microbiology, Clinical Research, Pharmacology, Pharmaceutical Sciences, or related disciplines.
Experience & Skills
- Freshers or candidates with up to 6 months of experience in analyzing clinical reports or scientific content.
- In-depth knowledge of clinical trials, pharmaceutical drug pipelines, and drug development phases.
- Strong understanding of therapeutic areas and trial design concepts.
- Excellent English written and verbal communication skills.
- Ability to interpret complex scientific and clinical information.
- Strong analytical and problem-solving mindset.
- Experience in secondary research related to clinical information is an added advantage.
Candidates who demonstrate attention to detail and strong data validation skills will thrive in this environment.
Location & Employment Details
- Location: Hyderabad, Telangana, India
- Work Mode: Hybrid (Monday to Friday)
- Working Hours: 9:00 AM to 6:00 PM
- Employment Type: Full-Time
- Job ID: JREQ134953
Application Process
Interested candidates can apply through the official Clarivate careers portal using the link below:
Applicants are encouraged to highlight academic knowledge of clinical trials, drug development lifecycle, and any relevant internships or research projects.
Frequently Asked Questions (FAQs)
1. Is this role open to freshers?
Yes, fresh graduates with strong knowledge of clinical trials and drug development are eligible.
2. Is prior clinical research experience mandatory?
No, up to 6 months of relevant experience is sufficient, but strong academic knowledge is essential.
3. What databases will the candidate work on?
The role involves Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence platforms.
4. Is the position fully remote?
No, it is a hybrid role based in Hyderabad.
5. What skills are critical for success?
Strong analytical ability, attention to detail, clinical trial knowledge, and clear communication skills.
Summary Table
| Company | Clarivate |
| Vacancies | Associate STEM Content Analyst |
| Required Education | B.Pharm, M.Pharm, MSc Biotechnology, MSc Microbiology, BSc Biotechnology, BSc Microbiology, Life Sciences |
| Experience | Freshers or up to 6 months in clinical report analysis |
To apply for this job please visit careers.clarivate.com.
