IQVIA
20+ DHL Supply Chain Interview Questions and Answers
Q1. What is Pharmacovigilance, Difference between ADR and ADE, Seriousness criterias, Medical significant meaning, one task was given to tell the chronological order of narrative writing, Regulatory authorities of...
read moreQ2. 1. Types of dimensions 2. What is the use of staging layer 3. How MDM testing is performed 4. How to find the day if date is given
Q3. What is the importance of Phase 3 Clinical trials, and what is the document that is signed by Study Subjects to show their agreement to participate willingly in a clinical trial?
Phase 3 Clinical trials are crucial for determining the safety and efficacy of a new treatment before it can be approved for public use. Study Subjects sign an Informed Consent document to show their agreement to participate willingly.
Phase 3 Clinical trials are the final stage of testing before a new treatment can be approved for public use.
These trials involve a larger group of participants to further evaluate the safety and efficacy of the treatment.
Study Subjects sign an ...read more
Q4. What do you mean by Pharmacovigilance role? What are AE and casualty? Authority of CLINIC TRAILS in the world?
Q5. CLINIC TRAILS? What are ICH GCP GUIDELINES? NAMES OF DICTIONARY OF CLINIC TRAILS AND WHY THEY ARE USED?
Q6. What are the Key Stakeholders involved in a Clinical trial?
Key stakeholders in a clinical trial include sponsors, investigators, participants, regulatory authorities, and ethics committees.
Sponsors: Provide funding and resources for the trial
Investigators: Conduct the trial and collect data
Participants: Individuals who volunteer to participate in the trial
Regulatory authorities: Ensure compliance with regulations and guidelines
Ethics committees: Review and approve the trial protocol to protect participant rights
Q7. Why add covariates to a Cox model in a randomized trial
Q8. Describe organizing tasks based on daily updates. Ensuring data accuracy in Excel/Access. Experience with analytical duties and quality control. Handling discrepancies in data documentation. Demonstrating flexi...
read moreQ9. 2-What is pharmacokinetics and pharmacodynamics?
Q10. What survival analysis methods I had used
Q11. 0.03 p value is significant? Why and how?
Q12. What was my FDA submission experience
Q13. differnece between innovator drugs, and generic drugs
Innovator drugs are brand-name drugs developed by pharmaceutical companies, while generic drugs are copies of innovator drugs made after the patent expires.
Innovator drugs are developed by pharmaceutical companies and have a brand name.
Generic drugs are copies of innovator drugs and are usually cheaper.
Generic drugs can only be made after the patent for the innovator drug expires.
Both innovator and generic drugs must meet the same FDA standards for safety and effectiveness.
Ex...read more
Q14. Phases of clinical trail, knowledge of clinical trail.
Q15. 13 Principles of ICH GCP E6 R2
The 13 Principles of ICH GCP E6 R2 are guidelines for conducting clinical trials in a way that ensures the safety and well-being of participants.
Principle 1: Clinical trials should be conducted in accordance with ethical principles.
Principle 2: The rights, safety, and well-being of trial subjects are the most important considerations.
Principle 3: The available non-clinical and clinical information should support the proposed trial.
Principle 4: The trial should be scientifical...read more
Q16. Estimate at Completion (EAC)
Q17. Phases of Clinical Trial
Phases of Clinical Trial involve different stages of testing a new drug or treatment.
Phase 1: Small group, safety and dosage testing
Phase 2: Larger group, effectiveness and side effects
Phase 3: Even larger group, compare to existing treatments
Phase 4: Post-marketing surveillance for long-term effects
Q18. Phases of clinical trials
Q19. Experience in flow Cytometry
Experience in flow cytometry is essential for this role, as it involves analyzing cells and particles in a fluid stream.
Hands-on experience with flow cytometers and related software
Ability to design and optimize flow cytometry experiments
Knowledge of different flow cytometry applications, such as cell counting, cell sorting, and biomarker analysis
Experience in analyzing and interpreting flow cytometry data
Troubleshooting skills for flow cytometry instrumentation and data anal...read more
Q20. Pharmaceutical Experience
Q21. Phases of clinical trail
Q22. Clinical trial phases
Q23. ICH GCP Guidelines
ICH GCP guidelines are international standards for the design, conduct, performance, monitoring, auditing, recording, analysis, and reporting of clinical trials.
Established by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)
Provide a unified standard for the European Union, Japan, and the United States
Emphasize the protection of human subjects and the quality and reliability of trial data
Cover aspects such as ethics...read more
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