Clarivate Content Editor – Clinical Trials Info Job For MSc Biotech, Life Sciences & Microbiology Candidates
Clarivate Content Editor – Clinical Trials Info Job For MSc Biotech, Life Sciences & Microbiology Candidates. MSc Life Sciences, Microbiology and Biotechnology Job. Apply online for the Content Editor – Clinical Trials Info 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 Content Editor – Clinical Trials Info 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: Content Editor – Clinical Trials Info
Job Number: JREQ121692
City, ST: Chennai, TN
Associate/Content Editor in the Clinical Trials team
We are looking for an Associate Content Analyst/Content Analyst to join our Clinical Trails team in Hyderabad/Chennai/Bangalore. This is an amazing opportunity to work on Cortellis Clinical Trial Intelligence and Cortellis Drug Discovery Intelligence. We have a great skill set in Clinical and we would love to speak with you if you have skills in Clinical/Drugs
About You
- Education (BPharm/MPharm/MSc in Biotechnology, Microbiology, Lifesciences)
- Work experience (2 to 3 year of experience in analyzing and updating clinical reports)
- Knowledge, skills, or abilities (In-depth knowledge of clinical trials, pharmaceutical drug pipelines, drug development and clinical phases)
- Excellent English written and verbal communication skills.
It would be great if you also had . . .
- Experience in secondary research related to clinical information
What will you be doing in this role?
- Maintain Clarivate database with up-to-date and accurate Clinical trials information from a range of information sources
- Accountable for the delivery of weekly targets
- You have to analyze, cross-reference, and update all new or previously updated information in the records of the Clinical trial from various sources, which includes company websites, presentations, conferences, Press releases, clinical trial repositories, and other possible internet sources.
- Ensure quality standards are observed
- Ability to understand and interpret complex and detailed Trials & Drugs related information from source material
About the Team
The team works for the product Cortellis Clinical Trial Intelligence and Drug Discovery Intelligence. The team size is 12 which includes Principal content analyst, Senior content analysts, Content analysts and Associate content analysts reporting to Rosary L – Team manager.
Hours of Work
9 hours per day, IST (including one hour break)
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 Content Editor – Clinical Trials Info at Clarivate
Interview Question 1: What experience do you have in analyzing and updating clinical reports?
Answer: I have 2-3 years of experience in analyzing and updating clinical reports. During my previous work experience, I was responsible for analyzing clinical trial data and updating the relevant information in the database accurately and on time. I have a strong understanding of clinical trials, drug development, and clinical phases.
Interview Question 2: How do you ensure the accuracy and quality of the data you input into the database?
Answer: To ensure the accuracy and quality of the data, I cross-reference and verify the information from various sources such as company websites, presentations, conferences, press releases, clinical trial repositories, and other internet sources. I also check the information multiple times and make sure that it meets the quality standards.
Interview Question 3: Can you tell us about your experience with secondary research related to clinical information?
Answer: Yes, I have experience in conducting secondary research related to clinical information. I have used various research databases and tools to gather relevant information related to clinical trials, drug development, and other related topics. I have also analyzed and interpreted the data to extract meaningful insights.
Interview Question 4: How do you manage your workload and meet weekly targets?
Answer: I prioritize my tasks based on their importance and urgency. I create a daily to-do list and ensure that I complete the tasks on time. I also regularly communicate with my team and manager to discuss any challenges and seek guidance if needed. Additionally, I try to manage my time efficiently to ensure that I meet the weekly targets without compromising on quality.
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