Clarivate MSc Biotech, Microbiology, Life Sciences Associate/Content Editor Job

Clarivate MSc Biotech, Microbiology, Life Sciences Associate/Content Editor Job

Clarivate MSc Biotech, Microbiology, Life Sciences Associate/Content Editor Job. MSc Life Sciences, Microbiology and Biotechnology Job. Apply online for the Associate/Content Editor in the Clinical Trials team 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 in the Clinical Trials team 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 in the Clinical Trials team

Job Number: JREQ121692

City, ST: Chennai, TN

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 is 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 the 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.

APPLY ONLINE

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 in the Clinical Trials team at Clarivate

1. Can you describe your experience in analyzing and updating clinical reports, and how it will help you in this role as a content editor in the Clinical Trials team?
   Answer: Yes, I have 2-3 years of experience in analyzing and updating clinical reports. In my previous role, I was responsible for maintaining the database with up-to-date and accurate clinical trials information. This involved analyzing, cross-referencing, and updating information from various sources, such as company websites, presentations, conferences, press releases, clinical trial repositories, and other internet sources. This experience has given me a good understanding of the clinical trial landscape, drug pipelines, drug development, and clinical phases.
2. How do you ensure the quality standards are observed while updating the database with clinical trials information?
   Answer: To ensure quality standards, I follow a thorough process of verifying the accuracy and consistency of the information before updating the database. I cross-check the information from multiple sources and ensure that all the data is complete and up-to-date. Additionally, I maintain a keen eye for detail and regularly review the updated records to ensure that they meet the highest quality standards.
3. Can you describe how you stay up-to-date with the latest clinical trials information and developments?
   Answer: To stay up-to-date with the latest clinical trials information and developments, I regularly attend industry conferences, webinars, and other events. I also subscribe to industry publications and newsletters and follow leading researchers and clinicians on social media. Additionally, I make use of various online resources, such as PubMed, ClinicalTrials.gov, and other clinical trial registries, to ensure that I am up-to-date with the latest developments in the field.
4. How do you handle tight deadlines and ensure timely delivery of the assigned targets?
   Answer: To handle tight deadlines and ensure timely delivery of assigned targets, I prioritize my work based on the urgency and importance of each task. I make use of productivity tools such as calendars and to-do lists to keep track of my tasks and ensure that I am working efficiently. Additionally, I communicate proactively with my team members and managers to ensure that I am on track to meet the deadlines and flag any potential issues well in advance.

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