Job Summary
CapeStart is seeking three highly motivated Associate Life Science Research Analyst Interns to join our Research & Analysis department in Nagercoil, Tamil Nadu. This internship provides a comprehensive foundation in clinical research, regulatory documentation, and scientific evidence generation. It is an ideal opportunity for final-year students in Pharmacy, Life Sciences, Biotechnology, or Public Health to gain hands-on experience in systematic literature reviews (SLR), clinical data validation, and the preparation of regulatory dossiers.
Key Responsibilities
As an intern, you will work closely with subject matter experts and cross-functional teams to contribute to high-impact research projects. Your primary responsibilities will include:
- Literature Reviews: Conducting systematic literature reviews, including article screening and rigorous data extraction.
- Evidence Synthesis: Assisting in the validation of clinical data and synthesizing complex scientific findings.
- Regulatory Documentation: Supporting the drafting and preparation of Common Technical Documents (CTD) and other regulatory submissions.
- Scientific Reporting: Preparing high-quality value dossiers, scientific summaries, evidence tables, and professional presentations.
- Data Formatting: Converting raw scientific data into structured, accurate, and regulatory-compliant formats.
Requirements
We are looking for candidates who possess a strong academic foundation and a keen interest in clinical research.
- Education: Currently in the final year of a Bachelor’s, Master’s, or PhD program in Pharmacy (B.Pharm/M.Pharm), Life Sciences, Biotechnology, Public Health, or a related discipline.
- Technical Skills: A solid understanding of research methodology, clinical data validation, and scientific writing.
- Knowledge Base: Familiarity with the basics of regulatory affairs and Common Technical Documents (CTD) is highly desirable.
- Analytical Ability: Strong skills in evidence organization, logical reasoning, and attention to detail.
Career Scope
This internship is designed to serve as a stepping stone toward a successful career in the life sciences sector. Upon completion, interns will be well-positioned for roles such as:
- Clinical Trial Assistant (CTA)
- Regulatory Affairs Associate
- Medical Writer
- HEOR (Health Economics and Outcomes Research) Analyst
- Pharmacovigilance Associate
Benefits
- Stipend: Competitive monthly stipend ranging from ₹10,000 to ₹20,000.
- Mentorship: Exposure to industry experts and direct experience with real-world regulatory and clinical projects.
- Professional Development: Development of core industry skills, including technical writing, data synthesis, and professional communication.
Selection Process
CapeStart utilizes a competency-based evaluation to identify top talent. The selection process consists of the following stages:
- Resume Screening: Assessment of academic background, research projects, and scientific writing proficiency.
- Aptitude Test: A 30-minute computer-based test covering mathematics, English grammar, and logical reasoning.
- Technical Interview: A comprehensive evaluation (approx. 3 hours) focusing on research methodology, literature review processes, and scientific documentation.
- Panel Interview: Assessment of professional attitude, communication skills, and learning mindset.
- Manager Interview: Evaluation of technical performance, attention to detail, and ability to collaborate effectively.
- Director Interview: A final review focused on long-term potential, professionalism, and cultural fit.
How to Apply
Interested candidates who meet the eligibility criteria are encouraged to apply by visiting our official careers portal. Please ensure your resume highlights any relevant coursework in biostatistics, pharmacology, or clinical research, as well as any final-year projects involving data analysis or scientific writing.
[Apply Here via the CapeStart Careers Portal]