Clinical Research Coordinator

Clinical Research Coordinator Interview Questions and Answers for Freshers

Updated 29 Feb 2024

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Q1. 3. What is Clinical Research 4. Responsibilities of Clinical Research Coordinator

Ans.

Clinical research involves studying the safety and effectiveness of medical treatments and interventions on human subjects.

  • Designing and implementing clinical trials

  • Recruiting and screening potential study participants

  • Collecting and analyzing data

  • Ensuring compliance with ethical and regulatory guidelines

  • Communicating with study sponsors and investigators

  • Managing study budgets and timelines

Q2. What are the steps done in clinical research

Ans.

Clinical research involves several steps from planning to publication of results.

  • Planning and designing the study

  • Obtaining necessary approvals and funding

  • Recruiting and enrolling participants

  • Collecting and analyzing data

  • Interpreting and reporting results

  • Publication and dissemination of findings

Q3. What do you know about Clinical trials.

Ans.

Clinical trials are research studies that test new medical treatments, drugs, or devices on humans.

  • Clinical trials are conducted to determine the safety and efficacy of new medical treatments, drugs, or devices.

  • They are typically divided into four phases, with each phase testing the treatment on a larger group of people.

  • Clinical trials are regulated by government agencies, such as the FDA in the United States.

  • Participants in clinical trials must give informed consent and may ...read more

Q4. What is informed consent

Ans.

Informed consent is a process of obtaining permission from a patient or participant after providing them with all relevant information.

  • Informed consent involves providing the patient or participant with information about the study, including its purpose, risks, benefits, and alternatives.

  • The patient or participant must be able to understand the information provided and make an informed decision about whether or not to participate.

  • Informed consent is an ongoing process and the...read more

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Q5. What is CR How many phase What is ICH GCP

Ans.

CR stands for Clinical Research. There are typically four phases in clinical trials. ICH GCP is a set of guidelines for conducting clinical trials.

  • CR stands for Clinical Research, which involves conducting trials to test the safety and efficacy of new treatments.

  • There are typically four phases in clinical trials: Phase 1, Phase 2, Phase 3, and Phase 4.

  • ICH GCP stands for International Conference on Harmonisation Good Clinical Practice, which is a set of guidelines for conducti...read more

Q6. What is clinical researcher

Ans.

A clinical researcher is a professional who conducts scientific studies to investigate new treatments, drugs, or medical devices.

  • Conducts scientific studies to investigate new treatments, drugs, or medical devices

  • Collects and analyzes data to determine the safety and effectiveness of interventions

  • Works closely with healthcare providers, patients, and regulatory agencies

  • Ensures that research is conducted ethically and in compliance with regulations

  • Communicates findings through...read more

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