Clarivate Clinical Trials Intelligence Job For MSc Biotech, Life Sciences & Microbiology – Apply Online

Clarivate Clinical Trials Intelligence Job For MSc Biotech, Life Sciences & Microbiology – Apply Online

Clarivate Clinical Trials Intelligence Job For MSc Biotech, Life Sciences & Microbiology – Apply Online. MSc Biotech, Life Sciences & Microbiology candidates can apply for Clarivate job openings. Interested and eligible applicants can check out all of the details on the same below

Possible interview questions for the Content Editor – Clinical Trials Intelligence position are posted below:

Content Editor – Clinical Trials Intelligence

Job Number: JREQ121694

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 AM to 6PM 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 

Possible interview questions for the Content Editor – Clinical Trials Intelligence position:

1. Can you describe your experience in analyzing and updating clinical reports? How did you ensure accuracy and data integrity in your previous role? Answer: In my previous role, I was responsible for analyzing and updating clinical reports by extracting relevant information from various sources such as company websites, presentations, conferences, and clinical trial repositories. To ensure accuracy and data integrity, I implemented a rigorous verification process, cross-referencing the collected information with multiple reliable sources. I also paid close attention to detail and followed established quality standards to maintain the integrity of the database.
2. How familiar are you with clinical trials, pharmaceutical drug pipelines, and the different phases of drug development? Can you give an example of how this knowledge has been applied in your previous work? Answer: I have in-depth knowledge of clinical trials, pharmaceutical drug pipelines, and the different phases of drug development. In my previous role, this knowledge was essential in understanding the context and relevance of the information I analyzed and updated. For instance, when updating clinical trial records, I needed to accurately classify the trial based on its phase, understand the drug’s mechanism of action, and interpret the trial’s objectives and endpoints. This knowledge helped me ensure that the database contained comprehensive and accurate information for users.
3. How do you approach maintaining a large database with up-to-date and accurate clinical trials information? Can you share your strategies for managing deadlines and delivering weekly targets? Answer: Maintaining a large database with up-to-date and accurate clinical trials information requires a systematic approach. I prioritize tasks based on their importance and urgency, ensuring that I allocate sufficient time for data collection, verification, and updates. To manage deadlines and deliver weekly targets, I set milestones and create a schedule to track progress. Additionally, I maintain clear communication with team members to collaborate effectively and address any challenges that may arise.
4. Can you discuss your experience in conducting secondary research related to clinical information? How did you gather and evaluate data from various sources to support your research findings? Answer: In my previous role, I conducted secondary research to gather additional clinical information from reputable sources such as scientific journals, publications, and databases. I utilized search strategies and keywords specific to my research objectives to retrieve relevant data. I critically evaluated the gathered information for reliability, credibility, and relevance to ensure its suitability for supporting research findings. Additionally, I maintained proper referencing and documentation practices to uphold the integrity of the collected data.
5. How do you approach understanding and interpreting complex and detailed trials and drugs-related information from source material? Can you provide an example of a challenging piece of information you had to analyze and how you tackled it? Answer: When faced with complex and detailed trials and drugs-related information, I adopt a systematic approach. I carefully read and analyze the source material, breaking down complex concepts into manageable parts. I make use of medical and scientific terminologies, references, and external resources to enhance my understanding. In a previous project, I encountered a clinical trial publication with intricate statistical analyses. To tackle it, I consulted statistical experts, reviewed relevant literature, and sought clarification from the authors when necessary. This collaborative effort allowed me to comprehensively grasp and interpret the complex information accurately.

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