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Team Manager, Stem Content Analysis

5+ years
Not Disclosed
10 April 30, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Team Manager, STEM Content Analysis - JREQ131214
Location: Chennai and Noida, India (Hybrid work model)
Department: Life Sciences & Healthcare
Job Type: Permanent contract


About the Role

We are seeking a Team Manager, Pharmacovigilance to join our Life Sciences & Healthcare team. You will lead a team responsible for curating drug safety information collected from journals, congress publications, and drug regulatory approvals. This information will be delivered to OFF-X, a translational drug safety intelligence portal. As the Team Manager, you will foster a culture of success, drive performance, and ensure the timely and high-quality delivery of key content.


Responsibilities

  • Create a culture of success, motivating and developing colleagues to reach their full potential.

  • Drive execution and performance by ensuring key performance indicators (KPIs) for quality, timeliness, and completeness are met, striving for continuous improvement.

  • Build a customer-focused team, encouraging an environment that fosters innovation.

  • Contribute to major decisions and initiatives that help the Content Function achieve its long-term goals.

  • Communicate initiatives to senior management, setting timelines and managing expectations for deliverables and releases.

  • Collaborate with Product, Product Operations, Technology, and Marketing teams in the product development process.

  • Identify opportunities for synergies and process simplification.


Qualifications & Experience

Required:

  • Degree in Life Sciences (Toxicology, Pharmacology, Biology, Pharmacy, Biomedical Sciences, etc.).

  • At least 5 years of experience in pharmacovigilance, drug safety management, and/or toxicology within a global corporation (pharma domain or consulting), including people and process management experience.

  • Strong written and oral communication skills in English.

Desired:

  • Demonstrated ability to work collaboratively in a matrixed organization.

  • Strong decision-making skills and ability to set priorities.

  • Ability to analyze processes, identify problems, and develop effective solutions.

  • Capability to work remotely with international peers.

  • Strong attention to detail, able to dive deep into content and results.


About the Team

You’ll report to the Director, Content Editing based in France and will join a dynamic, creative, and supportive team of over 80 colleagues, mostly based in Spain and India. You will work closely with around 20 colleagues in the OFF-X team, which is primarily based in India. The team culture is centered around excellence, integrity, and care, with a commitment to diversity and inclusion.

You will have access to 40 annual paid volunteering hours and be part of an active community that supports diverse initiatives across the business.


Work Hours

  • Full-Time: 40 hours per week


Equal Employment Opportunity

Clarivate is committed to providing equal employment opportunities for all individuals. We comply with all applicable laws and regulations regarding non-discrimination in employment.