Clarivate Clinical Studies Job For MSc Biotech, Microbiology – Apply Online
Clarivate Clinical Studies Job For MSc Biotech, Microbiology – Apply Online. MSc Biotechnology, 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 Studies position are posted below:
Content Editor – Associate/Content Editor – Clinical Studies Team
Job Number: JREQ123022
City, ST: Hyderabad, TG
Associate/Content Editor – Clinical Studies Team
As an Associate/Content Editor in Clinical team, you will be responsible for actively seeking out information about Clinical Studies, analyze, cross reference, and update all new or previously updated information in the clinical records from various sources, which includes scientific meetings, conferences, trial registries, press releases and other possible internet sources.
We are looking for an Associate Content Editor /Content Editor to join our Clinical Studies team in Hyderabad. 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)
- Work experience (0 – 1 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
- Ensure quality standards are observed
- Ability to understand and interpret complex and detailed Trials & Drugs related information from source material
- An inquisitive, analytical mind with strong problem-identification and solving skills
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.
Possible interview questions for the Content Editor – Clinical Studies Team position:
- Can you describe your experience and approach to actively seeking out information about clinical studies from various sources? How do you ensure the reliability and accuracy of the information you gather? Answer: In my previous role, I actively sought out information about clinical studies by regularly monitoring scientific meetings, conferences, trial registries, press releases, and other credible internet sources. I utilized effective search strategies, curated relevant data, and cross-referenced the information from multiple sources to ensure reliability and accuracy. Additionally, I critically evaluated the credibility and validity of the sources to maintain the integrity of the clinical records.
- How do you approach the task of analyzing and updating clinical records? Can you explain your process and attention to detail in ensuring the completeness and consistency of the information? Answer: When analyzing and updating clinical records, I follow a systematic process. I thoroughly review the existing information and compare it with new updates or previously updated data from various sources. I pay close attention to detail, ensuring the completeness and consistency of the information by verifying facts, cross-referencing data, and aligning it with established guidelines. I also ensure that the data is accurately entered into the database, maintaining the quality standards set for the clinical records.
- How do you handle complex and detailed information related to trials and drugs? Can you provide an example of a challenging piece of information you had to interpret and how you effectively communicated it? Answer: When faced with complex and detailed information related to trials and drugs, I employ a systematic approach. I carefully review the source material, break it down into manageable components, and seek additional resources or subject matter experts if needed. In a previous project, I encountered a clinical study with intricate statistical analyses. I collaborated with statisticians, referred to relevant literature, and conducted thorough research to ensure a comprehensive understanding. I then effectively communicated the findings by summarizing and presenting the information in a clear and concise manner, ensuring that it was easily comprehensible to the intended audience.
- How do you ensure the delivery of weekly targets while maintaining the quality standards of the clinical records? Can you share your strategies for managing your workload and meeting deadlines? Answer: To ensure the timely delivery of weekly targets while maintaining quality standards, I prioritize tasks based on their urgency and importance. I create a schedule and establish milestones to track progress and meet deadlines. Additionally, I regularly assess my workload, identifying potential bottlenecks or areas where additional support may be needed. Effective time management, organization, and effective communication within the team are essential in managing the workload and meeting deliverables without compromising the quality of the clinical records.
- Can you discuss your experience in understanding and interpreting complex trials and drugs-related information from source material? How do you stay updated with the latest advancements in clinical studies to enhance your understanding? Answer: In my previous role, I frequently encountered complex trials and drugs-related information. To enhance my understanding, I employ a systematic approach, carefully reviewing the source material and breaking down complex concepts into manageable components. I also stay updated with the latest advancements in clinical studies through continuous learning and engaging with relevant literature, attending conferences, and participating in professional development opportunities. This allows me to stay abreast of emerging trends, new methodologies, and advancements in the field, enabling me to effectively understand and interpret complex information from source material.
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