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Associate STEM Content Analyst | BPharm/MPharm/MSc | Clarivate Careers
Clarivate
Associate STEM Content Analyst | Clarivate Careers
Apply for Associate STEM Content Analyst at Clarivate. BPharm/MPharm/MSc graduates with 2+ years experience in clinical research. Hybrid role.
Are you a life sciences professional with a strong background in clinical research and pharmaceutical pipelines? Clarivate is inviting applications for the role of Associate STEM Content Analyst. This position is ideal for graduates in pharmacy, biotechnology, microbiology, and related life sciences who have experience in clinical research, data analysis, and content curation. Join a global leader in healthcare intelligence and contribute to advancing clinical trial insights that impact drug development worldwide.
Company Overview
Clarivate is a trusted global leader in providing actionable intelligence and analytics that accelerate innovation in the life sciences and healthcare industries. Through products like Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence, Clarivate enables researchers, pharmaceutical companies, and healthcare organizations to make informed decisions that shape the future of medicine. With a commitment to accuracy, transparency, and innovation, Clarivate supports breakthroughs that improve patient outcomes and global healthcare standards.
Working at Clarivate means joining a diverse and collaborative team of experts dedicated to providing cutting-edge information solutions. Our mission is to empower innovators and ensure that clinical and scientific knowledge benefits communities worldwide.
Job Role & Responsibilities
As an Associate STEM Content Analyst, you will play a crucial role in ensuring high-quality updates and accuracy of clinical trial records. Your day-to-day responsibilities will include:
- Analyzing, cross-referencing, and updating clinical trial records from multiple sources such as company websites, press releases, conferences, and trial repositories.
- Performing secondary research to track pharmaceutical drug pipelines and trial developments.
- Maintaining awareness of ongoing developments in assigned therapeutic or technology areas.
- Recording performance metrics against defined targets.
- Supporting the team to ensure deadlines and deliverables are consistently achieved.
- Maintaining accuracy, consistency, and compliance with internal quality standards.
- Taking ownership of training and continuous professional development in new technologies.
- Participating in process improvement initiatives and adapting to workflow changes.
- Collaborating effectively with content specialists, senior analysts, and cross-functional stakeholders.
This role is an opportunity to combine your scientific expertise with data-driven content analysis, contributing to Clarivate’s global knowledge platforms that power pharmaceutical and biotech innovations.
Eligibility / Qualifications
To be successful in this role, candidates must meet the following requirements:
- Education: BPharm, MPharm, M.Sc in Biotechnology, Microbiology, Life Sciences, or related fields.
- Experience: Minimum 2 years of experience in analyzing and updating clinical trial reports.
- Strong knowledge of clinical trials, pharmaceutical drug pipelines, drug development, and clinical phases.
- Excellent English communication skills (both written and verbal).
- Proficiency in content analysis, research methodologies, and handling multiple data sources.
Preferred Skills:
- Experience in secondary research related to clinical trial or pharmaceutical data.
- Strong analytical ability to delve deep into trial results and interpret scientific content.
- Effective planning and time management skills.
- Flexibility to adapt to changing processes and project requirements.
Relevant Courses: BPharm, MPharm, M.Sc Biotechnology, M.Sc Microbiology, M.Sc Life Sciences, Clinical Research, Pharmaceutical Sciences
Location & Salary
- Work Mode: Hybrid (remote flexibility available)
- Locations: Available across 2 locations (specific office locations shared during recruitment process)
- Work Hours: Full-time, 8 hours per day, Monday to Friday
- Employment Type: Permanent
- Salary: Competitive, aligned with industry standards, plus employee benefits and career development opportunities
Application Process
If you are passionate about clinical research content analysis and want to be part of a global healthcare intelligence provider, apply today.
- Apply Here: Clarivate Careers Portal
- Job ID: JREQ133450
Early applications are encouraged as shortlisting is in progress. Apply before the closing date to secure your chance to join Clarivate’s expert content team.
FAQs
Q1: What qualifications are required for this role?
A1: Candidates should hold BPharm, MPharm, or M.Sc in Biotechnology, Microbiology, Life Sciences, or equivalent fields, with at least 2 years of clinical data analysis experience.
Q2: Is this a remote job?
A2: The role is hybrid, offering a balance of remote work flexibility and office-based collaboration.
Q3: What kind of work will I be doing?
A3: You will analyze and update clinical trial records, track pharmaceutical pipelines, and ensure high-quality content for Clarivate’s clinical trial intelligence products.
Q4: Does Clarivate provide equal opportunities?
A4: Yes, Clarivate is an equal opportunity employer, committed to diversity and inclusion in all aspects of employment.
Q5: What is the team structure like?
A5: You will be working with a 20-member team consisting of content specialists, senior analysts, and associate analysts supporting Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence.
Vertical Summary Table
| Category | Details |
|---|---|
| Company | Clarivate |
| Vacancies | Associate STEM Content Analyst (Multiple) |
| Required Education | BPharm, MPharm, M.Sc Biotechnology, M.Sc Microbiology, M.Sc Life Sciences, Clinical Research |
| Experience | Minimum 2 years in clinical research content analysis and reporting |
To apply for this job please visit careers.clarivate.com.