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Freshers CRA Job Openings at Advarra – Apply on Biotecnika
If you are a life science fresher aiming to begin your career in clinical research, this opportunity is worth exploring. Freshers CRA Job Openings at Advarra – Apply on Biotecnika highlights an excellent entry-level role for graduates interested in clinical trials, regulatory compliance, and research operations. Designed for recent graduates, these CRA openings at Advarra offer structured training, hands-on exposure, and a clear pathway into the clinical research industry, making it an ideal starting point for aspiring clinical research professionals.
Job Title: Research Consultant (Clinical Research Associate)
Company Name: Advarra
Experience: Freshers 2025 – 2026 Graduate
CTC: 20k per month Post 3-month training 3.6LPA
Number of vacancies: above 20
Rounds of interview: 1 Virtual interview & 1 offline interview
Qualification: D.Pharm | B.Pharm | M.Pharm |
B.Sc (Biotechnology / Microbiology / Biochemistry / Genetics / Life Sciences) |
M.Sc (Biotechnology / Microbiology / Biochemistry / Genetics / Life Sciences)
Location: Bangalore
Job Summary:
Advarra is hiring Research Consultants (Clinical Research Associates) to support clinical trial activities through protocol interpretation, documentation, budgeting, and system-based project tracking. This entry-level role offers structured in-office training and a clear pathway to a full-time Research Associate position for fresh Life Science graduates.
Key Responsibilities:
• Interpret clinical trial study protocols to develop project-specific study calendars.
• Design and prepare site budgets based on clinical trial agreements and sponsor-provided financials.
• Develop and maintain Case Report Forms (CRFs) in alignment with trial and protocol requirements.
• Gain hands-on proficiency in CTMS and EDC systems to support study execution and deliverables.
• Use internal software tools to manage, monitor, and track project workflows and timelines.
• Ensure timely completion of assigned tasks while maintaining accuracy and quality standards.
• Collaborate closely with team members and reporting managers on daily and weekly assignments.
• Participate in team meetings, contributing to protocol-specific planning and execution strategies.
• Support clinical data management, trial coordination, and pharmacovigilance-related activities.
• Maintain proper records and documentation in compliance with GCP, SOPs, and regulatory guidelines.
Note – 1
The interview process will include an online assessment in the 2nd week of February, followed by an in-person interview at the Bangalore office in the 3rd week of February, with selected candidates expected to join Advarra in the 1st week of March (dates to be finalized).
CLICK HERE TO APPLY ONLINE
