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PHARMA JOBS POST > Advarra Hiring Research Analyst I – Exciting Opportunity for Freshers in Clinical Research | Bengaluru

Advarra Hiring Research Analyst I – Exciting Opportunity for Freshers in Clinical Research | Bengaluru

ADMIN
Last updated: June 13, 2025 3:26 am
ADMIN 22 hours ago
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  • Bengaluru - IND
  • Posted 22 hours ago
Advarra

Advarra

Location: Bengaluru, India 
Job Category: Research
Requisition Number: RESEA003576
Experience Level: 0–2 years


About Advarra

Advarra is a trailblazer in the clinical research industry, committed to advancing human health through ethical review services, cutting-edge technology, and unmatched industry expertise. As a market leader, Advarra is breaking barriers in clinical research by uniting patients, research sites, sponsors, and CROs to accelerate clinical trials and bring innovative treatments to life.

Company Culture

At Advarra, people are at the core of everything we do. Our values—Patient-Centric, Ethical, Quality-Focused, Collaborative—are reflected in our work every day. We foster a culture of inclusion, respect, and collaboration, empowering our employees to grow and make meaningful contributions. Join a team that works with empathy, urgency, and purpose to help improve lives globally.


Job Overview: Research Analyst I

As a Research Analyst I, you will support clinical trial projects by interpreting complex study documents and leveraging Advarra’s Clinical Trial Management Software (CTMS). Your role will be essential in ensuring project efficiency, content optimization, and communication across cross-functional teams.


Key Responsibilities:

  • Review and extract information from clinical trial documents.

  • Utilize CTMS features to support project design and development.

  • Collaborate with internal teams and project managers to meet deadlines and quality benchmarks.

  • Participate in meetings and contribute to protocol discussions.

  • Perform content review and repurposing to enhance productivity.

  • Address issues/bugs with a solution-driven mindset.


Qualifications

Basic:

  • Knowledge of clinical research processes, ICH GCP, and relevant industry regulations.

  • Ability to work both independently and collaboratively.

  • Proficient in MS Office and other business tools.

Preferred Experience (0–2 years):

  • Clinical trial coordination

  • Clinical data management

  • Pharmacovigilance

  • Records management

Preferred Skills:

  • Strong interpersonal and communication skills

  • High energy, proactive attitude, and cultural adaptability

  • Strong customer support orientation


Working Conditions

  • Hybrid model – Bangalore-based candidates preferred

  • Ability to work at a desk for extended periods

  • Light physical duties (up to 10 lbs.)

  • Focused, task-driven mindset required


Why Advarra?

Advarra offers an opportunity to be part of an organization that is changing the face of clinical research. Whether you’re a fresh graduate or an early-career professional, this is your chance to build a fulfilling career with purpose.


📝 Apply today and be a part of the change in clinical research

APPLY HERE

To apply for this job please visit recruiting.ultipro.com.

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