Clarivate MSc Life Science, Biotech, Microbiology & Biophysics Job Opening, Apply Online
Clarivate MSc Life Science, Biotech, Microbiology & Biophysics Job Opening, Apply Online. MSc Biotech, Biophysics, Biochem, Microbiology and Life Sciences Job. Apply online for the Drug Safety Associate Content Specialist 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 the role of Drug Safety Associate Content Specialist 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: Drug Safety Associate Content Specialist
Job Number: JREQ122057
City, ST: Noida, UP
Job Summary
We are looking for Associate Drug Safety Content Specialist to join our Pharmacovigilance (PV) team (offices working in Hybrid model). This is an amazing opportunity to support the team to perform literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs, therapeutic areas, and pharmacovigilance regulations.
Joining our team of PV Literature Screening, you will support the team in the analysis of Literature citations for individual case safety reports (ICSRs) as well
as other potential safety-relevant information impacting the risk-benefit and/or safety profile of customers’ products.About You – experience, education, skills, and accomplishments
- Master’s Degree in Life Sciences, Health or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.).
- A degree in Dentistry/physiotherapy/Nursing, which involves patient exposure in hospital-based environment, would be an advantage
- At least 1-2 years of experience reviewing biomedical literature for adverse event reporting
- OR equivalent combination of education and experience (i.e., an information science degree with at least 1 year of relevant working knowledge of supporting drug and patient safety)
- Related experience in drug safety/ pharmacovigilance is desirable
- Strong analytic ability to analyze and summarize the main points of biomedical case reports, studies, or specific topics
- At least 1 year of experience using writing skills to support the creation of succinct, accurate, and precise summaries
- At least 1 year of working knowledge of biomedical terminology, drugs, and therapeutic areas
It would be great if you also had the following:
- Certification from a professional medical writer’s association
- Experience with commercial and client-specific biomedical literature databases
- Scientific/medical writing background
What will you be doing in this role?
- Critically analyses large numbers of articles from biomedical published literature and internal drug safety alerts and identifies individual case safety reports (ICSRs) as well as other potential safety-relevant information impacting the risk-benefit and/or safety profile of customer’s products, as per applicable regulatory requirements and standard operating procedures.
- Writes brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article.
- Demonstrates understanding of client’s drug labels and uses that knowledge effectively when performing the safety assessments.
- Completes drug safety reviewing of each biomedical literature batch in a timely, thorough, and accurate manner in accordance with the client’s timeliness standards and quality.
- Uses a drug safety system to track all actions and assessments in an audit-ready reference history.
- Selects articles specific to the client’s interest for inclusion in the client’s product literature database per guidelines.
- Writes accurate, detailed, and complete abstracts of selected articles using good judgment regarding the level of detail required and excellent organization, grammar, and syntax.
- Extracts key points of articles and creates comprehensive and detailed indexes of the abstract contents to ensure precise and complete retrieval of literature from the client’s database.
- Ensures timely completion of indexing and abstracting of articles for assigned drugs in accordance with regulatory submission deadlines.
- Maintains an awareness of new drugs and new therapeutic categories, new disease entities, and changes in biomedical terminology in the published literature.
About the Team
The PV Literature team supports multiple customers covering all therapeutic areas. It is a supportive working environment with personalized training, and opportunities to engage in different aspects of pharmacovigilance and participate in customer upgrade planning if desired.
Hours of Work
This is a full-time permanent position working weekdays (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 Drug Safety Associate Content Specialist at Clarivate
- Can you tell us about your experience in reviewing biomedical literature for adverse event reporting?
Answer: Yes, I have 1-2 years of experience in reviewing biomedical literature for adverse event reporting. I have a master’s degree in Life Sciences, Health or Biomedical Sciences, which has provided me with the knowledge and skills required for this position.
- What is your experience with commercial and client-specific biomedical literature databases?
Answer: I have experience working with commercial and client-specific biomedical literature databases. I have used these databases to retrieve articles and to ensure that articles meet the guidelines for inclusion in the client’s product literature database.
- Can you describe a time when you had to complete drug safety reviewing of each biomedical literature batch in a timely, thorough, and accurate manner?
Answer: Yes, I can describe a time when I had to complete drug safety reviewing of each biomedical literature batch in a timely, thorough, and accurate manner. During my previous position, I was responsible for reviewing a large number of articles from biomedical published literature and internal drug safety alerts. I ensured that each batch was reviewed thoroughly and accurately, and I met the client’s timeliness standards and quality.
- How do you stay updated on new drugs and new therapeutic categories, new disease entities, and changes in biomedical terminology in the published literature?
Answer: I stay updated on new drugs and new therapeutic categories, new disease entities, and changes in biomedical terminology in the published literature by regularly reading scientific journals and attending conferences and webinars. I also stay in touch with colleagues in the industry to stay updated on the latest developments.
- Can you give an example of a time when you had to write an accurate, detailed, and complete abstract of a selected article?
Answer: Yes, during my previous position, I was responsible for writing accurate, detailed, and complete abstracts of selected articles. I used good judgment regarding the level of detail required and excellent organization, grammar, and syntax. One example was when I wrote an abstract of an article about a new drug that had just been approved for a specific therapeutic area. The abstract provided a detailed overview of the drug’s efficacy and safety profile.
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