Advarra is a trailblazer in the world of clinical research, committed to advancing human health through ethical review services and cutting-edge technology solutions. As an industry pioneer, Advarra connects stakeholders—including patients, clinical trial sites, sponsors, and Contract Research Organizations (CROs)—to accelerate clinical trials. The company’s mission-driven culture fosters inclusivity and collaboration, creating an environment where diverse perspectives are embraced and employees are empowered to make meaningful contributions.
At the core of Advarra’s operations are its values: Patient-Centric, Ethical, Quality Focused, and Collaborative. These values guide every decision, ensuring the company’s efforts impact clinical trial participants positively and facilitate better health outcomes for society.
Job Responsibilities
As a Research Associate II at Advarra, you’ll play a crucial role in supporting clinical trials and advancing research. Below is an overview of the primary responsibilities:
- Protocol Interpretation: Understand and interpret clinical trial study protocols to develop study calendars and budgets.
- Budget Management: Create site budgets based on clinical trial agreements and sponsor budgets.
- Case Report Form Design: Develop case report forms that align with study protocols.
- Software Utilization: Gain familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) to design budgets, calendars, and case report forms.
- Task Tracking: Use internal management software to track and manage weekly assignments.
- Collaboration: Participate actively in team meetings and contribute insights to discussions related to customer cases or protocols.
Qualifications
Advarra seeks individuals who are passionate about clinical research and possess the following qualifications:
- Basic Requirements:
- A minimum of 1+ year of relevant experience in clinical research.
- Knowledge of clinical research methodology, industry regulations, and Good Clinical Practice (GCP) guidelines.
- Ability to work both independently and in team environments.
- Proficiency in MS Office and other business tools.
- Preferred Qualifications:
- Experience as a Clinical Trial Coordinator or in Clinical Data Management.
- Familiarity with pharmacovigilance and records management processes.
Skills Required
- Strong Organizational Skills: Ability to manage multiple tasks and meet deadlines efficiently.
- Administrative Abilities: Handle documentation and compliance tasks meticulously.
- Team Player: Collaborate effectively with peers and managers in a hybrid work environment.
- Attention to Detail: Focus on high-quality work while interpreting complex protocols and budgets.
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