Job Description - Associate Research Analyst (PUB00004221)
Associate Research Analyst-PUB00004221
Description
Responsible
for the production, quality and functionality of specific content sets.
Participates in specialist interpretation in the form of research,
analysis, and writing to support the development and maintenance of
Thomson Reuters information in all media, and ensures that published
information contains premium content. Using scientific expertise and
ability, interprets and implements policy and applies defined processes.
Over time, builds on obtaining a working knowledge of the policies and
processes. Identifies key scientific issues in editorial material.
Classifies scientific information in the form of abstracts, texts,
reports, articles, indexes and highlights. Adheres to editorial
publishing schedules and quality standards along with guidance from the
supervisor. Works on obtaining on the job scientific knowledge required
to complete work and stay current on scientific trends and developments
related to the employee¿s editorial responsibilities.
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.
Position Overview :
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 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 skills
Qualifications
REQUIREMENTS:
Undergraduate / Post graduate Science degree from an accredited
institute Science educational background with an inclination towards
scientific research and writing. Ability to interpret, analyze, select,
organize, and communicate scientific material in preparation of content
sets. Gaining experience in understanding publishing workflow and its
impact on production, timeliness and product quality. Receives guidance
of the supervisor to manage and prioritize tasks.
REQUIRED Skills and Experience:
Basic knowledge of Clinical trials and Pharmacology
0-2 years of experience, Freshers Preferred
PREFERRED Skills and Experience : 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
Education / Certifications:
• B.Pharm., M .Pharm , M.Sc (Biotech ) - Preferably with basic
knowledge in Foreign Languages like Chinese, Korean, Japanese, Russian,
Portuguese
Job: Publishing/Editorial
Primary Location: India-Hyderabad-IND-Hyderabad-Solitaire
Organization:
GGO IP&S Gbl Editorial Content
Schedule: Full-time
Job Type: Standard
