Advarra is a leader in clinical research, dedicated to advancing human health through ethical review services, innovative technology, and deep industry expertise. The company bridges gaps in clinical research by connecting patients, sites, sponsors, and CROs in a unified ecosystem to accelerate clinical trials.
Company Culture
At Advarra, employees are at the heart of everything they do. The company fosters an inclusive, collaborative environment where respect, empathy, and diversity thrive. Their core values—Patient-Centric, Ethical, Quality-Focused, and Collaborative—guide their mission to improve clinical research, ensuring people live healthier, happier lives.
Job Description
Key Responsibilities:
- Interpret clinical trial protocols to design and develop study calendars.
- Analyze clinical trial agreements and sponsor budgets to create site budgets.
- Design case report forms (CRFs) for clinical trials.
- Work with Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) systems.
- Collaborate with managers to ensure high-quality deliverables.
- Track and manage tasks using internal case management software.
- Participate in team meetings and contribute to protocol discussions.
Basic Qualifications:
- Knowledge of clinical research methodology, GCP guidelines, and industry regulations.
- Ability to work independently and in a team.
- Strong organizational and administrative skills.
- Proficiency in MS Office and business software.
Preferred Qualifications:
- 0-1 year of internship experience in:
- Clinical trial coordination
- Clinical data management
- Pharmacovigilance
- Records management
- Excellent communication skills (written & verbal).
- High energy, proactive attitude, and passion for customer support.
Physical & Mental Requirements:
- Ability to sit/stand for extended periods.
- Lift up to 10 lbs occasionally.
- Strong focus, comprehension, and verbal communication skills.
How to Apply
