Are you passionate about clinical research and looking to make a meaningful impact in the healthcare industry? Advarra, a global leader in clinical research solutions, is hiring for the position of Business Operations Services Analyst in Bengaluru, India. This is a hybrid role, offering flexibility for remote work. If you have a background in clinical research and a desire to contribute to advancing human health, this could be the perfect opportunity for you. Read on to learn more about the role, responsibilities, and how to apply.
About Advarra
Advarra is a pioneer in the clinical research industry, dedicated to breaking down barriers that impede clinical trials. By aligning patients, sites, sponsors, and CROs in a connected ecosystem, Advarra accelerates the pace of clinical research. The company is known for its ethical review services, innovative technology solutions, and deep industry expertise.
At Advarra, employees are at the heart of everything they do. The company fosters an inclusive and collaborative environment where everyone is treated with respect and empowered to thrive. Their core values—Patient-Centric, Ethical, Quality Focused, and Collaborative—guide their mission to advance clinical research and improve lives.
Job Details
- Job Title: Business Operations Services Analyst
- Job Category: Research
- Requisition Number: RESEA003357
- Location: Bengaluru, India (Hybrid/Remote)
- Employment Type: Full-Time
- Posted Date: February 24, 2025
Key Responsibilities
As a Business Operations Services Analyst, you will play a critical role in supporting clinical trial operations. Your responsibilities will include:
- Protocol Interpretation: Understand and interpret clinical trial study protocols to design and develop calendars.
- Budget Development: Analyze clinical trial agreements and sponsor budgets to create site-specific budgets.
- Case Report Forms (CRFs): Design and develop CRFs for clinical trial study protocols.
- Software Utilization: Gain familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) systems to enhance calendar, budget, and CRF development.
- Collaboration: Work closely with your reporting manager to ensure all deliverables meet pre-determined quality criteria.
- Case Management: Use internal case management software to track and complete daily/weekly assignments efficiently.
- Team Participation: Actively contribute to team meetings and discussions related to customer cases and protocols.
Qualifications
Basic Qualifications:
- Knowledge of clinical research methodology, industry regulations, and Good Clinical Practice (GCP) guidelines.
- Ability to work independently and as part of a team.
- Strong organizational and administrative skills.
- Proficiency in MS Office and other business software.
Preferred Qualifications:
- 0-1 year of experience in roles such as:
- Clinical Trial Coordinator
- Clinical Data Management
- Pharmacovigilance
- Records Management
Physical and Mental Requirements
- Ability to sit or stand for extended periods.
- Capability to carry, raise, and lower objects weighing up to 10 lbs.
- Strong focus, attention to detail, and comprehension skills.
- Excellent verbal communication and listening skills.
Why Join Advarra?
Advarra is committed to creating a workplace where employees feel valued and empowered. The company offers:
- A collaborative and inclusive work environment.
- Opportunities to contribute to meaningful work that advances human health.
- Competitive compensation and benefits.
- A culture that prioritizes diversity, equity, and inclusion.
