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Clinical Trials Summer Internship

Join Clinical Trials summer internships to gain hands-on experience in the design, conduct, and analysis of clinical trials, focusing on regulatory compliance, trial protocols, and data management in healthcare research.

NTHRYS >> Services >> Academic Services >> Internships >> Summer Internships

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Clinical Trials Summer Internships

Join Clinical Trials summer internships to gain hands-on experience in the design, conduct, and analysis of clinical trials, focusing on regulatory compliance, trial protocols, and data management in healthcare research.
In 200+ Other Fields

More @ +91-8977624748
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Proj / Publications
Back to All Summer Internships.
Join our Clinicaltrials Publication Projects and earn co-authorship in the articles that will be published in Scopus Indexed or Science Citation Index (SCI) journals.

Focused Areas under Clinical Trials Summer Internship

  1. Clinical trial design and protocol development
  2. Regulatory compliance in clinical trials
  3. Data management and analysis in clinical trials
  4. Patient recruitment and retention strategies
  5. Good Clinical Practice (GCP) guidelines
  6. Clinical trial monitoring and auditing
  7. Safety reporting and adverse event management
  8. Statistical methods in clinical trials
  9. Ethical considerations in clinical trial conduct
  10. Phase I-IV clinical trials in drug development
  11. Randomized controlled trials (RCTs)
  12. Clinical trial data capture and management
  13. Informed consent and patient communication
  14. Blinding and randomization in trials
  15. Electronic data capture (EDC) in clinical trials
  16. Trial quality assurance and risk management
  17. Clinical trial logistics and site management
  18. Adaptive trial designs and implementation
  19. Real-world evidence (RWE) in clinical research
  20. Post-marketing surveillance and observational trials

Protocols Covered across various focussed areas under Clinical Trials Summer Internship

  1. Clinical trial protocol development and review
  2. Data capture and management in clinical trials
  3. Randomization and blinding techniques in trials
  4. Safety reporting and adverse event documentation
  5. Statistical analysis plans for clinical trials
  6. Electronic data capture (EDC) setup for clinical trials
  7. Good Clinical Practice (GCP) implementation
  8. Informed consent process and documentation
  9. Trial monitoring and auditing protocols
  10. Quality assurance in clinical trials

Duration: 5, 10, 15, 20, and 30 Days

Note: Please cross confirm whether internship slots for this field are available before joining.

Click Here for Clinical Trials Summer Internship Fees
Application Process and Other info
Note: Interns get complete handson exposure to all steps in the allocated methodology.
Fee, Application Process and Other Details: Please visit NTHRYS Internship Program Fees

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