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Advarra is hiring Research Analysts in Bengaluru. Join a global leader in clinical research driving innovation, ethics, and patient-focused excellence. Apply now for hybrid opportunities!
Job Category: Research
Requisition Number: RESEA003742
Location: Bengaluru, India (Hybrid Work Mode)
About Advarra
Advarra stands at the forefront of clinical research innovation, blending ethical review services with cutting-edge technology and deep industry expertise. As a global leader, Advarra is transforming the research landscape by aligning patients, sites, sponsors, and CROs within a connected ecosystem — accelerating clinical trials and advancing human health.
Our Culture
At Advarra, people are the heart of everything we do. Guided by our values — Patient-Centric, Ethical, Quality-Focused, and Collaborative — we act with urgency and purpose to make a meaningful difference in patients’ lives.
We foster an inclusive and respectful environment where every employee is empowered to grow, contribute, and thrive. Diversity of thought, empathy, and collaboration are key drivers of our success.
Position: Research Analyst
Job Type: Full-Time
Work Mode: Hybrid (Bengaluru, India)
Key Responsibilities
Interpret and analyze clinical trial study documents to extract necessary information.
Use Advarra’s Clinical Trial Management Software (CTMS) for project design, development, and support.
Collaborate with project managers and internal teams to meet agreed deliverables.
Review and repurpose existing content to enhance quality and efficiency.
Contribute to cross-functional teams, problem-solving, and process improvement.
Participate in team discussions related to specific protocols and client cases.
Maintain high standards of accuracy and quality in all deliverables.
Qualifications & Experience
Basic Qualifications
Strong knowledge of clinical research methodology, GCP, and ICH guidelines.
Good organizational and administrative skills.
Proficiency in MS Office and business software tools.
Ability to work independently and collaboratively.
Preferred Experience (0–2 years)
Clinical Trial Coordination
Clinical Data Management
Pharmacovigilance
Records Management
Preferred Skills
Excellent written and verbal communication skills.
Positive attitude, proactive approach, and teamwork mindset.
Passion for delivering exceptional support and innovative solutions.
Why Join Advarra?
At Advarra, you’ll contribute to advancing clinical research that improves lives globally. We offer a diverse and inclusive workplace, opportunities for professional growth, and the chance to be part of a team driving ethical and innovative clinical solutions.
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