Advarra, a leader in the clinical research industry, is on a mission to advance human health by accelerating clinical trials and breaking silos that impede research. With a robust foundation in ethical review services and innovative technology, Advarra creates a connected ecosystem aligning patients, sites, sponsors, and CROs. Join a company where patient-centric values and quality-focused approaches drive meaningful progress in clinical research.
Position: Research Analyst
Job Location: Bengaluru, India (Hybrid)
Employment Type: Full-Time
Posted Date: January 27, 2025
Key Responsibilities:
As a Research Analyst at Advarra, you will be a critical part of the clinical trial process, ensuring accuracy, efficiency, and compliance. Your responsibilities will include:
- Interpreting Clinical Trial Documents: Analyze and extract essential information from clinical trial study documents for various tasks.
- CTMS Utilization: Develop expertise in Advarra’s Clinical Trial Management Software (CTMS) to support project design, development, and execution.
- Project Management Support: Collaborate with project managers and teams to meet project requirements and ensure completion within deadlines.
- Content Optimization: Review and repurpose existing content to improve productivity and effectiveness.
- Cross-Functional Collaboration: Work seamlessly with teams to share ideas and resolve issues.
- Quality Assurance: Address issues and bugs while maintaining a detail-oriented approach to all tasks.
- Regular Task Completion: Coordinate with the reporting manager to complete daily and weekly tasks, ensuring adherence to quality standards.
- Team Participation: Actively contribute to team meetings, discussing specific customer cases and protocols.
Basic Qualifications:
To excel in this role, you should have:
- A solid understanding of clinical research methodologies and Good Clinical Practice (GCP) guidelines.
- Awareness of clinical trial industry standards, including ICH GCP.
- The ability to work independently and as part of a team.
- Strong organizational and administrative skills.
- Proficiency in MS Office and related business software.
Preferred Experience:
Candidates with 0–2 years of experience in the following areas are highly encouraged to apply:
- Clinical trial coordination.
- Clinical data management.
- Pharmacovigilance.
- Records management.
Preferred Qualifications:
- Highly personable and a team player.
- Excellent verbal and written communication skills.
- High energy and a positive attitude in diverse work environments.
- Proactive ownership of tasks with a solutions-oriented mindset.
Physical and Mental Requirements:
- Ability to sit or stand for extended periods.
- Capable of lifting objects up to 10 lbs.
- Strong focus and attention to detail.
- Effective verbal communication and comprehension skills.
