Freshers Join Advarra as Research Associate in Clinical Research

Advarra is a trailblazer in clinical research, dedicated to transforming the healthcare industry through innovative technology, ethical review services, and industry expertise. As a leader in clinical trials, Advarra aligns stakeholders—patients, sites, sponsors, and CROs—within a connected ecosystem to accelerate research and improve lives.

At Advarra, our mission is driven by a commitment to our values: Patient-Centric, Ethical, Quality-Focused, and Collaborative. Our inclusive work environment fosters respect, diversity, and empowerment, ensuring every team member thrives and contributes to impactful advancements in clinical research.

Responsibilities in the Job

As a Research Associate I at Advarra, you’ll play a pivotal role in supporting clinical trial activities:

1. Clinical Trial Protocols and Budgets
   • Interpret clinical trial study protocols to design and develop trial calendars.
   • Analyze clinical trial agreements and sponsor budgets to craft site-specific budgets.
2. Case Report Forms (CRFs) Development
   • Design case report forms in alignment with study protocols.
3. Utilization of Technology
   • Use Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software for efficient calendar, budget, and financial design.
4. Collaboration and Reporting
   • Partner with reporting managers to ensure timely and accurate completion of assignments.
   • Contribute to team discussions, offering insights on customer cases and protocols.
5. Administrative Tasks
   • Leverage case management software to track and complete assignments effectively.

Qualifications Required

Basic Qualifications

• Strong understanding of clinical research methodologies, industry regulations, and Good Clinical Practice (GCP) guidelines.
• Ability to work independently and collaboratively in a team setting.
• Proficiency in MS Office and other business software.

Preferred Qualifications

Candidates with 0-1 year of experience in the following areas are preferred:

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• Clinical trial coordination.
• Clinical data management.
• Pharmacovigilance.
• Records management.

Skills Needed

• Excellent organizational and administrative abilities.
• Strong attention to detail and task focus.
• Effective communication skills, both verbal and written.
• Ability to learn and apply basic instructions efficiently.

Application Link