Are you passionate about clinical research and advancing human health? Advarra, a leader in ethical review services and innovative technology solutions, is hiring for the position of Research Associate II. This full-time hybrid role based in Bengaluru, India, offers an exciting opportunity to contribute to cutting-edge clinical trials in a collaborative and inclusive environment.
About Advarra
Advarra is a pioneer in clinical research, committed to breaking down silos between patients, sites, sponsors, and CROs to create a connected ecosystem that accelerates clinical trials. Guided by core values of being Patient-Centric, Ethical, Quality-Focused, and Collaborative, Advarra is dedicated to fostering innovation and making a meaningful impact on human health.
With employees as the heart of the organization, Advarra values diverse perspectives and a culture of respect, empathy, and care. By advancing clinical research, the company empowers people to live healthier, happier lives.
Key Responsibilities
As a Research Associate III, your role will encompass designing and developing essential elements of clinical trial studies, utilizing innovative software, and collaborating across teams.
Your Main Duties Include:
- Protocol Analysis
- Interpret clinical trial study protocols to design and develop calendars and case report forms.
- Analyze clinical trial agreements and sponsor budgets to create site budgets.
- Software Expertise
- Gain proficiency in Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software.
- Utilize software tools to manage calendars, budgets, financials, and case report forms efficiently.
- Project Collaboration
- Participate actively in team meetings and discussions regarding specific customer cases or protocols.
- Coordinate with your reporting manager to meet daily and weekly quality targets.
- Tracking and Reporting
- Use internal case management and reporting software to track and complete assignments systematically.
Qualifications
Basic Requirements:
- Experience: At least 1+ years of relevant experience in clinical research or related fields.
- Knowledge: Familiarity with clinical research methodology, industry regulations, and Good Clinical Practice (GCP) guidelines.
- Skills: Strong organizational and administrative abilities, with proficiency in MS Office and business software.
Preferred Skills:
- Experience as a Clinical Trial Coordinator.
- Knowledge of Clinical Data Management, Pharmacovigilance, or Records Management.
Physical and Mental Requirements
- Ability to work at a stationary workstation for extended periods.
- Capability to manage tasks requiring focus, verbal communication, and adherence to basic instructions.
- Handle objects weighing up to 10 lbs.
