Content Specialist - Clinical -(Ext) Jobs in Hyderabad at Clarivate

Last Updated: Sep 11, 2021 05:10 IST


Company Name
Job title
Content Specialist - Clinical -(Ext)
3-4 Years
Not Mentioned

Job Profile

is a comprehensive resource to help you accelerate clinical trial planning including site selection, protocol design, biomarker identification and key competitive intelligence.
As we continue to proceed through this incredible transformation, we need experts with a zeal for innovation and who care deeply about delivering results to join the Clinical Trials Team. As a Principal Content Analyst/ Content Specialist in Clinical trials, you will be accountable for mastering Clinical content, driving process improvements, ensuring quality, and will be involved with the ongoing integration of this master with new content sets and other masters and workflows. If you think you fit, please consider an application for this position.
Main Purpose of Job:
  • Maintain Clarivate database with up-to-date and accurate Clinical trials information from a range of information sources with required levels of productivity
  • To embrace the hunt for ongoing opportunities, to optimize and automate, analysis and suggestions for process and content improvements of Clinical processes as part of your day-to-day role
  • To build up expertise in Clinical and their constituent facts such that you can recommend policies and processes to ensure a high level of data quality and consistency
  • To be involved in the hiring, training, and ongoing coaching of new team members
  • Draft documentation related to Clinical Content workflows and processes
  • To be an integral part of the Clinical team, collaborating with all stakeholders to facilitate smooth and timely execution of transition initiatives
  • To undertake quality control checking, resolve customer queries and correct data as required, identifying root causes of quality issues
  • Maintain Taxonomy
  • Undertake any other reasonable duties as requested by your manager on a permanent or temporary basis

Knowledge, Skills, and Abilities Required:
  • Expertise in Clinical & Drug content handling from various sources
  • An inquisitive, analytical mind with strong problem-identification and solving skills
  • Well organized and disciplined about policy, procedure, and standards
  • Confident and proactive team player, with good interpersonal skills
  • Good oral and written communication skills
  • Confidence in handling and interpreting data and clearly expressing findings
  • Ability to set priorities and be flexible in an ever-changing environment
  • Ability to work independently and efficiently with minimum/no supervision
  • Perseverance and courage to achieve goals even when circumstances are challenging
  • M.Pharm, or master's degree in Life Sciences
  • 3-4 yrs experience in Clinical content analysis, preferably at a pharmaceutical company, CRO or consulting/market research firm

It is the policy of Clarivate to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, pregnancy, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Clarivate will provide reasonable accommodations for qualified individuals with disabilities.

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Key skills
IT/ Computers - Software
is a comprehensive resource to help you accelerate clinical trial planning including site selection, protocol design, biomarker identification and key competitive intelligence. As we continue to proceed through this incredible transformation, we need
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