Selected intern’s day-to-day responsibilities include:
- Support the global regulatory affairs team in regulatory processes.
- Assist in the preparation and submission of regulatory documents.
- Ensure compliance with global regulatory standards and guidelines.
- Evaluate data and draw conclusions with guidance from senior team members.
- Maintain thorough documentation of all regulatory activities.
Earn certifications in these skills:
Learn Clinical Trial Analysis & Reporting
Who Can Apply
Only those candidates can apply who:
- Are available for full-time (in-office) internship.
- Can start the internship between 18th Jun’24 and 23rd Jul’24.
- Are available for the duration of 6 months.
- Have relevant skills and interests.
Women wanting to start/restart their career can also apply.
Other Requirements
- Experience: 0 to 2 years in the pharmaceutical industry, including areas such as drug safety, regulatory, clinical development, and medical affairs.
- Skills:
- Extensive knowledge of global regulatory processes, key pharmacovigilance regulations, and methodologies.
- Excellent English language skills (written and verbal), particularly in scientific/medical terminology.
- Proficiency in computer and IT skills, including web-based applications.
- Attributes:
- Good attention to detail.
- Strong interpersonal, presentation, and communication skills.
- Ability to work effectively in a team-oriented, interdisciplinary, and matrix environment.
- Service-oriented attitude, flexibility, and ability to prioritize work.
Our Values
The company focuses on values such as patient focus, transparency, respect, and integrity, along with a culture of innovation, performance, and trust. We are committed to delivering high-quality results, overcoming challenges, and focusing on what matters most. Our values drive our mission to unite science, technology, and talent to get ahead of disease together.
