Labcorp BSc MSc Life Sciences Data Reviewer Job, Apply Online
Labcorp BSc MSc Life Sciences Data Reviewer Job, Apply Online. BSc & MSc Life Sciences job opening. Labcorp hiring. Check out all the details on the same below:
Don’t forget to check out possible interview questions for this job below
Job Name: External Data Reviewer
Dept: Clinical
Location: Bangalore, India
Job Id: 2337306
Job Type: Full-Time
Labcorp Drug Development:
As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services paired with regulatory support for the chemical testing and crop protection industries.
Labcorp Drug Development is a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Our unique perspectives are based on decades of scientific, medical and regulatory expertise.
Did you know?
In July 2022, Labcorp announced its intention to spin off its clinical development business as a separate public company, subject to the satisfaction of certain customary conditions. Fortrea will become the new brand identity for our Clinical Development business in
connection with the spin-off, which is expected in mid-2023.We believe that the exceptional is possible when you have the right partner, so we are looking for the right people to help build a transformative force in Clinical Development. www.fortrea.com
Job Description:
- Ensure electronic lab data contains all protocol specified lab parameters, is in correct format and data populates to the specified fields and patients correctly.
- Review data discrepancies generated by study specific edit checks for laboratory data and assist in preparation of data clarification forms sent to the site or the central lab. Also, review missing/updated central laboratory data for potential request and substitution of local laboratory data.
- Perform 100% validation review of the electronically transmitted data for 5% of total number of patients in the study for loading purposes.
- Assist CDM Manager with review of laboratory edit checks, laboratory status reports and laboratory listings as necessary. Interact with Clinical staff (CTM/CRA) to obtain local laboratory normal ranges for all sites.
- Research and resolve discrepant information concerning the normal ranges, and maintain proper documentation. Enter and perform QC for local laboratory normal ranges.
- Verify the normal ranges are properly attached to the patient results in the local lab data collection module of the database.
- Perform other duties as required by the Department Responsible as contact person for the External source of electronic data transmissions.
- Keep the Central lab and client informed of problems involving data transfers, data point issues and validation issues.
Education/Qualifications:
- B.Sc/M.Sc Life Science or equivalent
Experience:
- 3-5 years of relevant experience.
Labcorp is proud to be an Equal Opportunity Employer:
As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.
💡 Here are a few possible interview questions for the above job posting and their answers.
👍We hope this helps in giving you a rough idea as to how to prepare for the interview for this specific role. Good luck!
- Can you explain your experience in ensuring electronic lab data accuracy and adherence to protocol specifications? How do you verify that data is in the correct format and populates to the specified fields accurately?
Answer: In my previous role as an External Data Reviewer, I was responsible for meticulously reviewing electronic lab data to ensure compliance with protocol requirements. I would cross-check the data against the specified parameters, ensuring that it was in the correct format and accurately populated in the respective fields. I would perform thorough validations and quality checks to ensure data integrity.
- How do you handle data discrepancies generated by study-specific edit checks for laboratory data? Can you describe your approach to preparing data clarification forms and reviewing missing or updated central laboratory data?
Answer: When encountering data discrepancies generated by study-specific edit checks, I would carefully analyze the discrepancies and investigate the root causes. I would then prepare data clarification forms, which would be sent to the site or central lab to address the issues. Additionally, I would review missing or updated central laboratory data to assess the need for requesting or substituting local laboratory data.
- Could you describe your process for performing validation reviews of electronically transmitted data? How do you ensure accuracy and quality during the loading process?
Answer: To ensure accuracy and quality, I would perform 100% validation reviews of electronically transmitted data for a representative sample, typically 5% of the total number of patients in the study. I would meticulously examine the data, verifying its integrity and alignment with study requirements. This thorough review allowed me to identify any potential issues or discrepancies before the data was loaded into the system.
- How do you collaborate with Clinical staff (CTM/CRA) to obtain local laboratory normal ranges for all sites? Can you explain your approach to researching and resolving discrepant information concerning normal ranges?
Answer: Collaboration with the Clinical staff was crucial in obtaining local laboratory normal ranges for all sites. I would communicate with the CTM/CRA to gather the necessary information and ensure the normal ranges were accurately recorded in the database. In cases where discrepant information arose, I would conduct thorough research, investigating the discrepancies and documenting the findings. I would resolve the issues by aligning the data with the appropriate normal ranges, maintaining meticulous documentation throughout the process.
- As the contact person for the external source of electronic data transmissions, how do you handle problems involving data transfers, data point issues, and validation issues? Can you describe your approach to keeping the central lab and clients informed?
Answer: As the contact person for external data transmissions, I am proactive in addressing problems that may arise. I maintain open lines of communication with the external source to promptly resolve any data transfer issues, data point discrepancies, or validation concerns. I collaborate with the central lab and clients, providing timely updates and maintaining transparency regarding the status and progress of the data-related matters. Clear and consistent communication ensures effective problem-solving and fosters strong partnerships with all stakeholders involved.
Note: These answers are provided as examples. It is essential to customize the answers based on personal experience and expertise.
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