Pharmacy Job at Clarivate | Apply Now for the STEM Content Analyst Role
Clarivate is hiring a Regulatory Intelligence Content Analyst for its Life Sciences Regulatory Intelligence team. This Pharmacy Job requires a candidate with a Bachelor’s degree in Life Sciences or Pharmacy and 3–5 years of experience in regulatory affairs or quality compliance. The successful applicant will monitor global health authority changes (FDA, EMA, WHO) and validate AI-generated regulatory content to maintain the integrity of Cortellis Regulatory Intelligence (CRI) modules.
- Job Title: STEM Content Analyst
- Location: 2 Locations (Hybrid)
- Job ID: JREQ134851
About The Company
Clarivate is a global leader in providing trusted insights and analytics to accelerate the pace of innovation. In fact, many professionals seeking a Pharmacy Job in regulatory intelligence have found rewarding roles with this team. The Regulatory Intelligence team is responsible for curating high-quality content across the full product lifecycle. Their flagship product, Cortellis Regulatory Intelligence (CRI), provides country-specific modules that support compliance and strategic planning for the global life sciences industry.
Requirements
- Bachelor’s degree in Life Sciences, Pharmacy, or another relevant field is required for this Clarivate Job.
- Minimum 3–5 years of experience in regulatory affairs, regulatory intelligence, pharmaceutical development, quality compliance, or related life sciences roles.
- Strong understanding of global and regional health authority frameworks (e.g., FDA, EMA, WHO, national Ministries of Health).
- Ability to interpret and synthesize regulatory requirements related to pharmaceuticals, biologics, advanced therapies, medical technologies, or digital health.
- Experience assessing legislation, guidance documents, and regulatory updates with strong analytical and contextual judgment.
- Familiarity with AI‑assisted editorial workflows or experience validating AI‑generated outputs.
- Excellent written communication, attention to detail, and editorial precision.
- Ability to work effectively with global, cross‑functional, and remote teams.
- Fluency in English; additional languages are an asset.
Aditional Requirements
- Prior experience developing regulatory intelligence or structured regulatory content. Additionally, those interested in a job in pharmacy will benefit from regulatory background.
- Knowledge of regulatory lifecycle management (submissions, approvals, post‑approval changes).
- Experience engaging with external consultants or local regulatory experts.
- Understanding of quality management principles, compliance frameworks, and information classification. This is especially relevant for anyone applying for a Pharmacy-related Job.
- Insight into AI/ML‑enabled content production or digital transformation initiatives in regulatory affairs.
Job Responsibilities
- Monitor global and regional regulatory developments from competent authorities, Ministries of Health, and international regulatory bodies.
- Interpret and contextualize complex regulatory updates across pharmaceuticals, biologics, medical technologies, digital health, and quality/manufacturing compliance. For anyone seeking a new Pharmacy Job, this will be a valuable responsibility to highlight on your resume.
- Transform regulatory changes into structured, high-quality intelligence for CRI’s country modules and internal databases.
- Conduct in-depth analysis of legislation, guidance, and consultations, identifying impacts on submissions, approvals, and lifecycle management.
- Collaborate with AI-enabled content production workflows to enrich content, improve efficiency, and apply expert oversight for quality assurance.
- Coordinate with external consultants and local experts to ensure accuracy and precision in country‑level regulatory information. Such collaboration is often part of a modern Pharmacy Job role.
- Communicate key regulatory insights to internal teams, editorial partners, and customer‑facing functions.
- Support cross‑functional initiatives, including:
- AI-assisted workflow optimization
- Product and feature enhancements
- Quality assurance and compliance improvements
- Global content harmonization



