Advarra is a leading clinical research organization that focuses on advancing human health through clinical research. With a rich history rooted in ethical review services and cutting-edge technology, Advarra is committed to breaking down barriers in clinical research, connecting patients, sites, sponsors, and CROs to accelerate trials. Their dedication to creating a connected ecosystem ensures that clinical trials are faster, more efficient, and ultimately benefit patients’ lives. Advarra fosters an inclusive, collaborative environment where employees thrive and contribute to the company’s mission of advancing health.
Responsibilities in the Research Associate II Job
As a Research Associate II at Advarra, you will play a pivotal role in supporting clinical research projects by performing a variety of tasks. Your responsibilities will include:
- Study Protocol Design: Interpreting clinical trial protocols to create and develop detailed study calendars.
- Budget Development: Collaborating with sponsors and understanding clinical trial agreements to assist in developing site budgets.
- Case Report Forms (CRFs): Designing and developing case report forms for clinical trials, ensuring they align with study protocols.
- Software Utilization: Familiarizing yourself with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software for calendar, budget, and CRF development.
- Team Collaboration: Actively participating in team meetings and contributing insights to customer cases and protocols.
- Tracking and Reporting: Using internal case management software to track work assignments and ensure completion in a timely manner.
Qualifications
To be considered for the Research Associate II role at Advarra, you should meet the following basic qualifications:
- 1+ Years of Relevant Experience: Ideally, you should have at least one year of experience in clinical research or related fields.
- Knowledge of Clinical Research: Understanding clinical research methodology, Good Clinical Practice (GCP) guidelines, and industry regulations.
- Organizational Skills: Strong administrative and organizational abilities.
- Familiarity with Software: Proficiency in MS Office and other business software for managing tasks and reporting.
Preferred Qualifications include:
- Experience as a Clinical Trial Coordinator at a clinical site.
- Background in Clinical Data Management or Pharmacovigilance.
- Familiarity with Records Management.
