Advarra stands as a beacon of innovation and ethics in the clinical research industry. With a robust legacy in ethical review services and cutting-edge technology solutions, Advarra has positioned itself as a pioneer in advancing human health. The company breaks down silos that hinder clinical research, creating a connected ecosystem that brings together patients, sites, sponsors, and CROs to accelerate trials. Guided by values such as being patient-centric, ethical, quality-focused, and collaborative, Advarra aims to advance clinical research for happier and healthier lives.
At Advarra, inclusivity and collaboration are not just ideals but fundamental practices. The company values diverse perspectives and ensures every employee feels respected, valued, and empowered to thrive. This commitment makes Advarra not only a leader in its field but also an excellent workplace.
Responsibilities in the Job
As a TEMP Research Consultant at Advarra, you will play a vital role in supporting clinical trials through meticulous planning and execution. Your key responsibilities will include:
- Designing and Developing Calendars: Interpret clinical trial study protocols to create detailed calendars.
- Budget Development: Analyze clinical trial agreements and sponsor budgets to draft site-specific budgets.
- Case Report Form Design: Create and design case report forms based on study protocols.
- Software Utilization: Leverage Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) tools to optimize calendars, budgets, financials, and case report forms.
- Quality Assurance: Ensure daily and weekly tasks meet predetermined quality criteria by closely collaborating with reporting managers.
- Case Management and Reporting: Use internal case management and reporting software for tracking and completion of assignments.
- Team Collaboration: Actively participate in team meetings and contribute to discussions about specific customer cases and protocols.
Qualifications
Basic Qualifications:
- Knowledge of clinical research methodology, industry regulations, and Good Clinical Practice guidelines.
- Ability to work independently and collaboratively in a team environment.
- Strong organizational and administrative skills.
- Familiarity with MS Office and various business software tools.
Preferred Qualifications:
- Internship experience (0-1 year) in areas such as:
- Clinical trial coordination at a site.
- Clinical data management.
- Pharmacovigilance.
- Records management.
- A team-oriented and personable approach.
- Excellent verbal and written communication skills.
- High energy with a positive attitude in a diverse work environment.
- A proactive approach with a strong sense of ownership.
Skills Required
- Proficiency in clinical trial methodologies.
- Familiarity with CTMS and EDC systems.
- Strong problem-solving and organizational abilities.
- Effective communication and interpersonal skills.
- Ability to adapt and perform in a dynamic, fast-paced environment.
