Research Associate II – Join Advarra’s Clinical Research Team
Are you a motivated clinical research professional looking to advance your career? Advarra, a global leader in ethical review, clinical trial technology, and research compliance, is seeking a Research Associate II to join our dynamic team in Bengaluru. This is a fantastic opportunity to contribute to impactful clinical trials while gaining hands-on experience with CTMS, EDC, CRFs, and clinical trial budgeting. If you have a passion for clinical research and a desire to work in a collaborative environment, we encourage you to apply.
Job Summary
The Research Associate II will support clinical trial startup activities, working closely with study protocols, clinical trial agreements, and eClinical systems. The role involves interpreting protocols, developing site budgets, configuring eClinical systems, managing workflows, and collaborating with team members to ensure quality and adherence to timelines.
Responsibilities
- Protocol and Document Interpretation:
- Interpret clinical trial study protocols to design comprehensive study calendars.
- Analyze clinical trial agreements (CTAs) and sponsor budgets to develop accurate site-level budgets.
- eClinical System Configuration:
- Design and develop Case Report Forms (CRFs) based on study requirements.
- Configure Advarra’s CTMS & EDC systems, including calendars, CRFs, budgets, and financial modules.
- Workflow Management:
- Track daily tasks and progress using internal case management tools.
- Ensure all deliverables meet internal quality standards and established timelines.
- Collaboration & Reporting:
- Collaborate with the reporting manager for task prioritization and guidance.
- Actively participate in team discussions to address protocol requirements and troubleshoot issues.
Requirements
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Basic Requirements:
- Minimum of 1+ year of experience in clinical research or a related field.
- Strong understanding of clinical research methodology, ICH-GCP guidelines, and relevant industry regulations.
- Ability to work independently and collaboratively within a team.
- Proficiency in MS Office suite and standard business software applications.
- Excellent organizational, communication, and interpersonal skills.
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Preferred Experience:
- Experience as a Clinical Trial Coordinator (CTC) is highly desirable.
- Experience in clinical data management, pharmacovigilance, or records management is a plus.
Benefits
Advarra is committed to providing a rewarding and supportive work environment. While specific benefits may vary, employees in similar roles typically enjoy the following:
- Competitive salary with opportunities for professional growth.
- Hybrid or remote work options to promote work-life balance.
- Comprehensive training on CTMS, EDC, and other advanced eClinical systems.
- A collaborative and inclusive work culture that values teamwork and innovation.
- Exposure to global clinical research standards and best practices.
Job Location
Bengaluru, India (Hybrid or Remote Eligible)
Salary (Estimated Range in INR)
₹4,50,000 – ₹7,50,000 per annum (This is an industry-aligned estimate for Research Associate II roles in India; actual salary may vary depending on experience and qualifications.)
How to Apply
Interested candidates are encouraged to apply through the following link: [Application Link]
We look forward to receiving your application!