At Advarra, we are dedicated to transforming the world of clinical research and advancing human health. With a strong foundation in ethical review services, cutting-edge technology solutions, and deep industry expertise, we are pioneers in breaking down barriers that slow down clinical trials. Our mission is to align patients, sites, sponsors, and CROs in a connected ecosystem to accelerate the development of life-saving treatments.
Our Culture:
Advarra’s employees are the heart of our success. We foster an inclusive, collaborative, and respectful workplace where diverse perspectives are valued. Guided by our core values—Patient-Centric, Ethical, Quality-Focused, and Collaborative—we strive to create an environment where every employee feels empowered to make a meaningful impact.
Job Description
As a Research Associate I at Advarra, you will play a critical role in supporting clinical trials by designing and developing essential study tools. This position is ideal for individuals passionate about clinical research and eager to contribute to the advancement of human health.
Key Responsibilities:
- Protocol Interpretation & Calendar Design:
- Understand and interpret clinical trial study protocols to design and develop study calendars.
- Analyze clinical trial agreements and sponsor budgets to create site-specific budgets.
- Case Report Form (CRF) Development:
- Design and develop case report forms for clinical trial study protocols.
- Software Utilization:
- Gain familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to enhance the design of calendars, budgets, and CRFs.
- Team Collaboration:
- Work closely with your reporting manager to ensure all deliverables meet pre-determined quality criteria.
- Actively participate in team meetings, contributing to discussions on customer cases and protocols.
- Reporting & Tracking:
- Use internal case management and reporting software to track and complete daily/weekly assignments efficiently.
Qualifications
Basic Qualifications:
- Knowledge of clinical research methodology, industry regulations, and Good Clinical Practice (GCP) guidelines.
- Ability to work independently and collaboratively in a team environment.
- 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 at a workstation.
- Regularly carry, raise, and lower objects weighing up to 10 lbs.
- Strong focus, attention to detail, and ability to comprehend instructions.
- Excellent verbal communication skills, including listening, understanding, and responding effectively.
Why Join Advarra?
- Be part of a market leader in clinical research innovation.
- Work in a supportive, inclusive, and collaborative environment.
- Contribute to advancing human health and improving lives globally.
- Opportunities for professional growth and development.
How to Apply
Application Link (Application Closed Dont Apply)
