Associate Content Editor

7 days ago

Hyderabad, India Clarivate Full time

We are looking for an Associate Content Editor to join our team in Hyderabad. This is an amazing opportunity to work on OFF-X, a translational drug safety intelligence portal. The team consists of 20 people located in Spain and India and is reporting to the Regulatory and drug safety manager line. We have a great skill set in the analysis of drug safety and toxicity data and we would love to speak with you if you have skills in pharmacovigilance and summary of data.

About You - experience, education, skills, and accomplishments
- At least 1 year of experience in pharmacovigilance and/or in editorial teams focused on scientific publications
- Proven knowledge of basic pharmacology and drug safety. An advanced level of English is also required.
- MS or PhD in pharmacology, toxicology, biochemistry, biotechnology, medicinal chemistry or a related biological science
- Excellent interpersonal, organizational skills and teamwork skills

It would be great if you also had...
- Familiarity with databases and scientific information systems
- Experience on writing regulatory documentation or scientific publications

What will you be doing in this role?
- Analysis and interpretation of published data (clinical trials, journal articles, reviews, meta-analysis, congress communications, drug approval reports, etc.)
- Collection and curation of information on risks and safety of drug products (recording, archiving, updating and evaluating the information)
- Writing case studies, reports and reviews
- Maintain informed discussions with experts and customers.

About the Team

Our editorial team is a group of 20 people creating and delivering content for OFF-X, a translational drug safety intelligence portal that allows user to easily identify new safety liabilities. We are a global team based on India and Spain with more than 50 years of experience in the sector. We create and classify content for more than 300 references every week, including Journals, Congress publications and Regulatory documents. In this team you will have the opportunity to be up-to-date with all the new advances in the drug development industry and you will be constantly learning new things.

Hours of Work

General Shift - 9 AM to 6 PM IST

We offer a full-time (40 hours/week) (Monday to Friday)

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.

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