MSc, BTech Bioinformatics, Mol Bio, Genetics, Biotech Job at Clarivate, Apply Online

Clarivate Bioinformatics Biotech Biochem Mol Bio Content Editor Job, Apply Online

Clarivate Bioinformatics Biotech Biochem Mol Bio Content Editor Job, Apply Online. MSc, BTech Genetics, Bioinformatics, Mol Bio, Biochem, 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 Associate Content Editor – GENESEQ
position are posted below:

Content Editor – Associate Content Editor – GENESEQ

Job Number: JREQ122587

City, ST: Chennai, TN

Associate Content Editor – GENESEQ

We are looking for Associate Content Editor/Content Editor to join our Geneseq process in Hyderabad or Chennai. This is an amazing opportunity to work on Geneseq process in IPG. We would love to speak with you if you have skills in Biotechnology, Bioinformatics, Microbiology, Genetics, Molecular Biology, and Biochemistry.

About You

• Master’s degree and/or BTech in Biotechnology, Bioinformatics, Microbiology, Genetics, Molecular Biology, and Biochemistry
• At least 1 year of experience in working on patents, patent indexing with basic patent knowledge. 
• Proven experience in patent indexing, disease indexing, abstract writing, effective communication, problem identification and solving skills, good interpersonal skills, adhere to change, effective time management, email etiquette, positive attitude and self-motivated with the ability to deliver consistently.
• Good knowledge on computer including MS office, PDF or TIFF images; good exposure to publicly available databases like NCBI taxonomy database, PubMed, etc; and secondary research skills.

It would be great if you also had . . . 

• 1 to 2 years of relative experience on patent indexing, gene sequencing, genetics, and disease indexing.
• MTech and/or Mphil/PhD.

What will you be doing in this role?

• Apply biotechnology, genetics, and molecular biology concepts to curate biological sequence related information from patent documents in line with editorial policies and conventions.
• Achieve weekly production volume and quality targets and to maintain the consistency.
• Taking an active role within the team to ensure targets are met.
• Maintain awareness of current developments in own technology areas.
• To make positive efforts to promote personal safety and that of others by taking reasonable care at work, by carrying out the requirements of the law or following recognized codes of practice provided or advised by management to ensure safe working practices.

About the Team  

GENESEQ Team is one of the key knowledge-driven processes in Intellectual Property Group in Clarivate. The team consists of 37 colleagues, in various roles with different experience and skill set in various domains like Biotechnology, Bioinformatics, Microbiology, Genetics, Molecular Biology, and Biochemistry; are reporting to a Team Manager. GENESEQ includes Nucleic Acid sequences of minimum 10 bases or 8 if claimed and Amino Acid sequences of minimum 4 residues.

GENESEQ Indexers manually curate all biological sequences given in the specification, including those found within PDF or TIFF images, not just those given in the formal electronic sequence listing. They also create additional sequences which are described in the specification, which often are not given in the sequence listing, but which are claimed. The team will also create individual records for mutated sequences and for claimed SEQ ID fragments where the whole sequence has not been claimed.

Hours of Work

Full time – 9 AM to 6 PM (includes 1 hour break), subject to slight changes based on business needs.

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.

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Possible interview questions for the Associate Content Editor – GENESEQ position:

1. Can you explain your experience and knowledge of patent indexing and disease indexing? How have you applied these skills in your previous role? Answer: In my previous role, I gained experience in patent indexing and disease indexing through working with patent documents and extracting relevant information. I have a thorough understanding of the indexing process, including the identification and categorization of key information such as genetic sequences and disease-related data. I have applied these skills by ensuring accurate and consistent indexing, adhering to editorial policies and conventions, and maintaining high-quality standards in my work.
2. How do you approach the curation of biological sequence-related information from patent documents? Can you discuss your attention to detail and adherence to editorial policies in this process? Answer: When curating biological sequence-related information from patent documents, I follow a systematic approach. I carefully analyze the documents to identify relevant sequences, such as nucleic acid and amino acid sequences. I pay close attention to detail, ensuring accurate transcription and representation of these sequences in line with editorial policies and conventions. I also verify the consistency and completeness of the information, ensuring that all relevant sequences are captured and recorded accurately.
3. Can you share an example of a challenging situation you encountered while curating biological sequences from patent documents? How did you address the challenge and ensure the accuracy of the information? Answer: In a previous project, I encountered a patent document with complex biological sequences that required meticulous attention to detail. The document contained both nucleic acid and amino acid sequences, as well as variations and fragments. To ensure accuracy, I utilized my knowledge and expertise in biotechnology, genetics, and molecular biology. I cross-referenced the sequences with existing databases and consulted relevant literature to verify their accuracy. I also sought clarification from subject matter experts when needed to address any ambiguities and ensure the completeness and precision of the curated biological sequences.
4. How do you manage your workload and ensure the achievement of production volume and quality targets in a timely manner? Can you discuss your strategies for effective time management and maintaining consistency in your work? Answer: Effective time management is crucial in managing workload and meeting production volume and quality targets. To achieve this, I prioritize tasks based on their urgency and importance, setting realistic deadlines and milestones. I utilize tools such as calendars and task lists to organize my work and ensure efficient allocation of time. Additionally, I maintain consistent attention to detail, adhering to established editorial policies and conventions, and conducting regular quality checks to maintain high standards of accuracy and completeness.
5. How do you stay updated with current developments in biotechnology, genetics, and molecular biology? Can you discuss your strategies for continuous learning and enhancing your knowledge in these areas? Answer: Staying updated with current developments is essential in the field of biotechnology, genetics, and molecular biology. I actively engage in continuous learning by regularly reading scientific journals, attending conferences, and participating in relevant webinars and workshops. I also subscribe to newsletters and follow reputable sources in the field to stay informed about the latest advancements, emerging trends, and evolving technologies. By dedicating time to continuous learning, I ensure that my knowledge remains up-to-date and relevant, enabling me to contribute effectively in curating biological sequence-related information from patent documents.

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