Clarivate MSc & PhD Biological Science, Biotech, Biochem Drug Safety Intelligence Editor Job
Clarivate MSc & PhD Biological Science, Biotech, Biochem Drug Safety Intelligence Editor Job. MSc, PhD Biological Science, Biotechnology, Biochemistry Job. Apply online for the Associate Content Editor – Drug Safety Intelligence vacancy at Clarivate. Interested and eligible applicants can check out all of the details on the same below:
Hey there, if you are interested in this role of Associate Content Editor – Drug Safety Intelligence at Clarivate then make sure you check out some interview questions along with their answers that we have listed at the bottom of the page
Job Title: Associate Content Editor – Drug Safety Intelligence
Job Number: JREQ121390
City, ST: Hyderabad, TG
Associate Content Editor – Drug Safety Intelligence
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
- 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.
We know you are here all eager and wanting all of the answers, so read on below to read and absorb some of the interview questions for the role of Associate Content Editor – Drug Safety Intelligence at Clarivate
- Can you describe your experience in pharmacovigilance and how you have applied your knowledge in analyzing drug safety and toxicity data? Answer: In my previous role, I worked in a pharmacovigilance team where I was responsible for analyzing and interpreting various types of published data, including clinical trials, journal articles, and drug approval reports. I utilized my understanding of pharmacology and drug safety to assess risks and evaluate the safety profile of drug products.
- How do you stay updated with the latest advancements in the drug development industry and scientific publications? Answer: I have developed a strong habit of continuous learning and staying updated with the latest advancements. I regularly follow reputable scientific journals, attend conferences, and engage with experts in the field. Additionally, I make use of databases and scientific information systems to access relevant information and stay informed about regulatory changes.
- Can you provide an example of a complex case study or report you have written in the field of drug safety? How did you approach the analysis and synthesis of the information? Answer: During my previous role, I worked on a comprehensive case study that involved analyzing multiple sources of data, including clinical trials, adverse event reports, and regulatory documents. I approached the analysis by thoroughly reviewing each piece of information, identifying key findings, and synthesizing the data into a cohesive report. This allowed for a comprehensive understanding of the safety profile of the drug in question.
- How do you ensure accuracy and reliability in your work when dealing with large volumes of scientific information? Answer: Accuracy and reliability are crucial in dealing with scientific information. To ensure this, I employ a systematic approach, including thorough data verification, cross-referencing multiple sources, and following established guidelines and standard operating procedures. I am also attentive to detail and take the time to validate and double-check my findings before finalizing any reports or publications.
- Can you describe a time when you faced challenges while working collaboratively with experts and customers? How did you handle the situation? Answer: In my previous role, I encountered a situation where there were differing opinions among experts regarding the interpretation of certain drug safety data. To handle this, I facilitated open and respectful discussions, allowing each expert to express their viewpoints. I actively listened, considered alternative perspectives, and worked towards finding a consensus. Ultimately, this collaborative approach helped in resolving the differences and ensuring the accuracy and completeness of the analysis.
Remember, these questions are just examples, and you can adapt them based on the specific requirements and context of the role.
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