At Thomson Reuters, we believe what we do matters. We are passionate about our work, inspired by the impact it has on our business and our customers. As a team, we believe in winning as one - collaborating to reach shared goals, and developing through challenging and meaningful experiences. With over 60,000 employees in more than 100 countries, we work flexibly across boundaries and realize innovations that help shape industries around the world. Making this happen is a dynamic, evolving process, and we count on each employee to be a catalyst in driving our performance - and their own.
Post: Associate Research Analyst
Job description
The Drug Information department is part of the Thomson Reuters’ Ip & Science Editorial Operations Group and comprises several teams responsible for the daily collection, synthesis and maintenance of data relating to investigational and marketed drugs, as well as the companies developing them. These records form a core element of the Thomson Pharma and Thomson Pharma Partnering drug information platforms.
The Clinical Trials Team is responsible for the identification and curation of information relating to ongoing and completed clinical trials; ie, when new and marketed drugs are tested in humans to identify its safety and efficacy in both healthy volunteers and patients. This part of the development process is a costly, yet essential, part of any drug's development. The Clinical Trials Team gathers and publishes data on the design of clinical trials ongoing around the world, and the results of those studies, providing critical intelligence for our customers. The main role of the editor in this team includes analysing press releases, scientific conference posters, scientific articles and online trial sites for clinical data with which to update our information products. In addition to clinical trial expertise, the editor will need to become well-versed in policy around updating the drug and company records, and may be required to expand their activities outside of the Clinical Trials team.
Essential Day-to-Day Responsibilities:
- Accountable for the delivery of weekly database filling milestones.
- Ensure quality standards are observed.
- Ability to understand and interpret complex and detailed clinical information from source material
. Ability to research and synthesise scientific information
. An inquisitive, analytical mind with strong problem-identification and -solving skillsWe are the leading source of intelligent information for the world's businesses and professionals, providing customers with competitive advantage. Intelligent information is a unique synthesis of human intelligence, industry expertise and innovative technology that provides decision-makers with the knowledge to act, enabling them to make better decisions faster. We deliver this must-have insight to the financial and risk, legal, tax and accounting, intellectual property and science and media markets, powered by the world's most trusted news organization.
Qualification: - B.Pharm., M .Pharm , M.Sc (Biotech)
Required Skills:
Basic knowledge of Clinical trials and Pharmacology. 0-2 years of experience, Freshers Preferred
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Attention to detail
- Computer and internet literacy with good keyboard skills
- Excellent English written and verbal communication skills and basic knowledge in Foreign Languages like Chinese, Korean, Japanese, Russian, Portuguese At Thomson Reuters, we believe what we do matters. We are passionate about our work, inspired by the impact it has on our business and our customers. As a team, we believe in winning as one - collaborating to reach shared goals, and developing through challenging and meaningful experiences. With over 60,000 employees in more than 100 countries, we work flexibly across boundaries and realize innovations that help shape industries around the world. Making this happen is a dynamic, evolving process, and we count on each employee to be a catalyst in driving our performance - and their own.
As a global business, we rely on diversity of culture and thought to deliver on our goals. To ensure we can do that, we seek talented, qualified employees in all our operations around the world regardless of race, color, sex/gender, including pregnancy, gender identity and expression, national origin, religion, sexual orientation, disability, age, marital status, citizen status, veteran status, or any other protected classification under country or local law. Thomson Reuters is proud to be an Equal Employment Opportunity/Affirmative Action Employer providing a drug-free workplace.
Additional Information:
Location: Chennai
Education: B.Pharm, M .Pharm, M.Sc (Biotech)
Industry Type: Pharma/ Biotech/Clinical Research
ID: JREQ012263
End Date: 17th Jan., 2014
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