Associate STEM Content Analyst

Posted 12 Hours Ago
Be an Early Applicant
Chennai, Tamil Nadu
Entry level
Analytics
The Role
The Associate Content Analyst will gather and update information on clinical trial Sites and Investigators from various sources, aiming to meet quality and production targets while collaborating with a small team. Responsibilities include performing secondary research, maintaining quality standards, and adapting to process changes.
Summary Generated by Built In

We are looking for an Associate Content Analyst to join our CT Investigators & Sites team in Chennai responsible for analyzing, cross-referencing, and updating all new or previously updated Sites and investigator information in the clinical trial records from a variety of sources, including company websites, presentations, conferences, press releases, clinical trial repositories, and other potential internet sources.

About You

  • Bachelor’s Degree in Lifesciences (Preferably in Pharmacy)
  • 0- 2 years’ experience in a global corporate setting and with a strong knowledge of Life science & Healthcare content.
  • In-depth knowledge of clinical trials
  • Demonstrated ability to work collaboratively in a matrixed organization.
  • Good judgment in decision-making and priority setting.
  • Excellent written and oral communication skills in English.

It would be great if you also had . . .  

  • Experience in secondary research related to clinical information
  • Ability to delve deep into content and results.

What will you be doing in this role? 

  • Actively gather and update information on Clinical trial Sites and Principal Investigators from various sources, including company websites, presentations, conferences, press releases, clinical trial repositories, and other internet sources.
  • Achieve production volume and quality targets
  • Recording of performance against target
  • Taking an active role within the team to ensure targets are met.
  • Stay informed about current developments in your technology areas.
  • Achieve and maintain consistent quality standards, Effective personal planning, and time management.
  • Maintain a flexible and adaptable approach to process changes.
  • Take responsibility for identifying your technology training and developmental needs on an ongoing basis
  • Perform any other reasonable duties as requested by your line manager/director on a permanent or temporary basis.

 About the Team  

The team works for the product Cortellis Clinical Trial Intelligence. The team size is 7 which includes Associate Content Analysts and Content Analysts.

Hours of Work  

8 hours per day (Full-Time, Permanent)

Workdays – Monday to Friday (Hybrid Model)

Location- Chennai

At Clarivate, we are committed to providing equal employment opportunities for all persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.

The Company
Belfast
10,549 Employees
On-site Workplace

What We Do

Clarivate™ is a global leader in providing solutions to accelerate the lifecycle of innovation. Our bold mission is to help customers solve some of the world’s most complex problems by providing actionable information and insights that reduce the time from new ideas to life-changing inventions in the areas of science and intellectual property. We help customers discover, protect and commercialize their inventions using our trusted subscription and technology-based solutions coupled with deep domain expertise. For more information, please visit clarivate.com.

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