Advarra is a pioneering leader in clinical research, dedicated to advancing human health through ethical review services, innovative technologies, and deep industry expertise. We bridge the gaps between patients, clinical trial sites, sponsors, and CROs, fostering a connected ecosystem to accelerate clinical trials. Our mission is to make a meaningful impact on global healthcare and create healthier futures for people worldwide.
Our Company Culture
At Advarra, employees are at the heart of everything we do. Our values—Patient-Centric, Ethical, Quality-Focused, and Collaborative—guide our daily actions and decisions. We promote an inclusive environment where diverse perspectives are welcomed, and every individual feels empowered to thrive. We treat our clients, trial participants, and colleagues with empathy and respect, knowing that our work significantly impacts patients’ lives.
Job Details
- Position: Research Associate I
- Location: Bengaluru, India (Remote/Hybrid)
- Job Category: Research
- Job Type: Full-Time
- Posted on: October 17, 2024
Key Responsibilities
- Study Protocol Design:
- Understand and interpret clinical trial protocols to design study calendars.
- Review trial agreements and sponsor budgets to develop site budgets for the protocol.
- Form Development:
- Design and develop case report forms (CRFs) based on trial study protocols.
- Software Utilization:
- Gain familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) systems for calendar, budget, and form design.
- Collaboration & Reporting:
- Work closely with the reporting manager to complete daily and weekly tasks related to budgets, financials, and CRFs.
- Utilize internal case management tools to track and complete assignments efficiently.
- Team Participation:
- Actively participate in team meetings and contribute meaningfully to discussions on protocols and customer cases.
Basic Qualifications
- Knowledge of clinical research methodology, industry regulations, and Good Clinical Practice (GCP) guidelines.
- Ability to work both independently and within a team environment.
- Strong organizational and administrative skills.
- Familiarity with MS Office and other business software tools.
Preferred Qualifications
- 0-1 year of experience in related fields, such as:
- Clinical trial coordination at research sites
- Clinical data management
- Pharmacovigilance
- Records management
Physical and Mental Requirements
- Ability to sit or stand for extended periods at a stationary workstation.
- Regularly handle and move objects up to 10 lbs.
- Ability to follow and comprehend basic instructions.
- Focused attention to detail and ability to meet deadlines.
- Verbal communication skills for listening, responding, and contributing effectively to discussions.
