Required Skills:
Basic knowledge of Clinical trials and Pharmacology
0-2 years of experience, Freshers Preferred.
Basic knowledge of Clinical trials and Pharmacology
0-2 years of experience, Freshers Preferred.
Post: Associate Research Analyst
Location: Chennai
Education: B.Pharm., M.Pharm, M.Sc (Biotech), M.Sc Biochemistry, M.Sc Clinical Biochemistry
Location: Chennai
Education: B.Pharm., M.Pharm, M.Sc (Biotech), M.Sc Biochemistry, M.Sc Clinical Biochemistry
Job Description:
The Drug Information department is part of theThomson Reuters’ Ip & Science Editorial Operations Group and comprisesseveral teams responsible for the daily collection, synthesis and maintenanceof data relating to investigational and marketed drugs, as well as thecompanies 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 theidentification and curation of information relating to ongoing and completedclinical trials; ie, when new and marketed drugs are tested in humans toidentify its safety and efficacy in both healthy volunteers and patients. Thispart of the development process is a costly, yet essential, part of any drug'sdevelopment. The Clinical Trials Team gathers and publishes data on the designof clinical trials ongoing around the world, and the results of those studies,providing critical intelligence for our customers. The main role of the editorin this team includes analysing press releases, scientific conference posters, scientificarticles and online trial sites for clinical data with which to update ourinformation products. In addition to clinical trial expertise, the editor willneed to become well-versed in policy around updating the drug and companyrecords, and may be required to expand their activities outside of the ClinicalTrials team.
Essential Day-to-Day Responsibilities:
- Accountable for thedelivery of weekly database filling milestones.
- Ensure quality standardsare observed.
- Ability to understand and interpret complexand detailed clinical information from source material
. Ability to research andsynthesise scientific information
. An inquisitive,analytical mind with strong problem-identification and -solving skills
We 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. - See more at: http://jobs.thomsonreuters.com/job/Chennai-Associate-Research-Analyst-Job/64882200/#sthash.iIsDqkXk.dpuf
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D
Job ID: JREQ019031
End Date: 25th June, 2014
The Drug Information department is part of theThomson Reuters’ Ip & Science Editorial Operations Group and comprisesseveral teams responsible for the daily collection, synthesis and maintenanceof data relating to investigational and marketed drugs, as well as thecompanies 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 theidentification and curation of information relating to ongoing and completedclinical trials; ie, when new and marketed drugs are tested in humans toidentify its safety and efficacy in both healthy volunteers and patients. Thispart of the development process is a costly, yet essential, part of any drug'sdevelopment. The Clinical Trials Team gathers and publishes data on the designof clinical trials ongoing around the world, and the results of those studies,providing critical intelligence for our customers. The main role of the editorin this team includes analysing press releases, scientific conference posters, scientificarticles and online trial sites for clinical data with which to update ourinformation products. In addition to clinical trial expertise, the editor willneed to become well-versed in policy around updating the drug and companyrecords, and may be required to expand their activities outside of the ClinicalTrials team.
Essential Day-to-Day Responsibilities:
- Accountable for thedelivery of weekly database filling milestones.
- Ensure quality standardsare observed.
- Ability to understand and interpret complexand detailed clinical information from source material
. Ability to research andsynthesise scientific information
. An inquisitive,analytical mind with strong problem-identification and -solving skills
We 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. - See more at: http://jobs.thomsonreuters.com/job/Chennai-Associate-Research-Analyst-Job/64882200/#sthash.iIsDqkXk.dpuf
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D
Job ID: JREQ019031
End Date: 25th June, 2014
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