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Freshers needed as Associate STEM Content Analyst at Clarivate

Published on

Clarivate

0 - 2 years

4.5 - 5 Lacs per year

Remote and On-site Chennai, Tamil Nadu, India

B Pharm, M Pharm, Pharm.D

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Clarivate is seeking a dedicated Associate Content Analyst to join the CT Investigators & Sites team. This role focuses on the in-depth analysis, cross-referencing, and updating of clinical trial information related to Sites and Principal Investigators. This position is perfect for someone passionate about life sciences and healthcare, with a keen interest in clinical research and data management.

About Clarivate

Clarivate is a global leader in providing trusted insights and analytics that help accelerate the pace of innovation. With comprehensive research solutions and a collaborative work environment, Clarivate is committed to supporting professionals who shape the future of various industries, including life sciences and healthcare.

Responsibilities in the Role

  • Research & Analysis: Actively gather and update information on clinical trial Sites and Investigators from diverse sources like company websites, presentations, press releases, and clinical trial databases.
  • Data Accuracy & Quality: Ensure data accuracy and meet production volume and quality standards.
  • Team Collaboration: Work collaboratively within the team to achieve collective targets and deadlines.
  • Performance Monitoring: Record and evaluate individual performance against set targets.
  • Continuous Learning: Stay up-to-date with the latest developments in clinical trials and related technology.
  • Flexible Adaptation: Maintain adaptability to changing processes and tasks as directed by management.
  • Training & Development: Take the initiative in identifying and pursuing opportunities for professional growth.

Qualifications Needed

  • Education: Bachelor’s degree in Life Sciences (preferably Pharmacy).
  • Experience: 0-2 years in a global corporate setting with a strong background in life sciences and healthcare content.
  • Knowledge: In-depth understanding of clinical trials and relevant content.
  • Skills:
    • Strong analytical and decision-making capabilities.
    • Excellent English communication skills (oral and written).
    • Ability to manage time effectively and plan personal work efficiently.
  • Desirable: Experience in secondary research of clinical information and the ability to thoroughly analyze content and outcomes.

Skills Required

  • Demonstrated ability to work collaboratively in a matrixed organization.
  • Proficiency in handling diverse data sources for content updates.
  • Strong organizational skills with attention to detail.
  • Effective problem-solving skills and the ability to set priorities.

Application Link