Clinical Trials & Research - Internship (WFH)

About the internship:Selected intern's day-to-day responsibilities include:

1. Learn the fundamentals of clinical research and clinical trial processes.

2. Understand the different phases of clinical trials.

3. Learn about clinical trial protocols and study documentation.

4. Understand the roles of sponsors, investigators, CROs, and other stakeholders.

5. Learn the basics of Good Clinical Practice (GCP).

6. Understand informed consent and ethical considerations in clinical research.

7. Learn about patient recruitment, eligibility criteria, and study procedures.

8. Understand clinical trial data collection and documentation.

9. Gain exposure to adverse event reporting and safety monitoring concepts.

10. Review sample clinical trial documents and case studies.

11. Participate in research-oriented assignments and discussions.

12. Apply the acquired knowledge to a capstone clinical research project during the third month.Who can apply:Only those candidates can apply who:are available for the work from home job/internshipcan start the work from home job/internship between 16th Sep'26 and 21st Oct'26are available for duration of 3 monthshave relevant skills and interestsStipend:INR₹ 8,000 - 25,000 /monthDeadline:[hidden]:59:59Other perks:Certificate, Letter of recommendation, Flexible work hours, 5 days a weekSkills required:Effective CommunicationOther Requirements:Candidates should be from pharmacy, B - Pharma Background only.About Company:Simpli Intern is a global online bootcamp and digital skills training provider that helps working professionals and students learn in-demand technical fields. It offers courses and certifications in fields like data science, AI, cyber security, and project management through partnerships with top universities and companiesAdditional information:

Stipend Structure:

Fixed pay: ₹ 5,000 - 15,000 /month

Incentive pay: ₹ 3,000 - 10,000 /month

Responsibilities

Selected intern's day-to-day responsibilities include:

1. Learn the fundamentals of clinical research and clinical trial processes.

2. Understand the different phases of clinical trials.

3. Learn about clinical trial protocols and study documentation.

4. Understand the roles of sponsors, investigators, CROs, and other stakeholders.

5. Learn the basics of Good Clinical Practice (GCP).

6. Understand informed consent and ethical considerations in clinical research.

7. Learn about patient recruitment, eligibility criteria, and study procedures.

8. Understand clinical trial data collection and documentation.

9. Gain exposure to adverse event reporting and safety monitoring concepts.

10. Review sample clinical trial documents and case studies.

11. Participate in research-oriented assignments and discussions.

12. Apply the acquired knowledge to a capstone clinical research project during the third month.