Advarra is a leader in the clinical research industry, known for its ethical review services and innovative technology solutions. With a mission to accelerate clinical trials, Advarra connects patients, research sites, sponsors, and CROs to drive industry change and improve human health. Advarra’s commitment to patient-centric, ethical, and quality-focused research has made it a pioneer in the field, ensuring every trial contributes to healthier, happier lives.
Company Culture
At Advarra, employees are the backbone of the company’s success. The organization fosters a collaborative, inclusive culture where diversity is embraced and respect is paramount. Guided by core values of empathy, care, and urgency, Advarra strives to make every team member feel valued and empowered to contribute to groundbreaking clinical research. The company provides a supportive environment where employees can thrive and make a meaningful impact on the clinical research landscape.
Job Responsibilities
As a Research Associate I at Advarra, you will play a crucial role in supporting clinical trials by:
- Designing and developing study calendars and site budgets based on clinical trial protocols and agreements.
- Creating case report forms tailored to the specific needs of each clinical trial.
- Utilizing Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to manage trial calendars, budgets, financials, and case report forms.
- Collaborating closely with your reporting manager to ensure all deliverables meet the company’s stringent quality standards.
- Tracking work assignments and ensuring timely completion using internal case management and reporting software.
- Actively participating in team meetings and contributing insights to improve customer cases and protocol management.
Qualifications
To succeed in this role, candidates should have:
- Basic knowledge of clinical research methodologies, industry regulations, and Good Clinical Practice (GCP) guidelines.
- The ability to work both independently and collaboratively in a team setting.
- Strong organizational and administrative skills.
- Familiarity with Microsoft Office and other business software.
Preferred Experience
Advarra prefers candidates with 0-1 year of experience in the following areas:
- Clinical trial coordination at research sites.
- Clinical data management.
- Pharmacovigilance.
- Records management.
Skills
- Strong understanding of clinical research protocols.
- Ability to design and manage clinical trial budgets and case report forms.
- Proficiency in CTMS and EDC software.
- Excellent organizational, communication, and teamwork abilities.
- Attention to detail and adherence to quality standards.
