Advarra Hiring Life Science Candidates. Apply Now!
Advarra, a leading research solutions provider, is seeking talented Life Science candidates for the position of Research Associate III. Join our dynamic team to contribute to cutting-edge research and make a meaningful impact in the field of life sciences.
Job Title: Research Associate III
Job Category: Research
Requisition Number: RESEA002342
Job Type: Full Time
Primary Duties and Responsibilities
- Understand and interpret clinical trial study protocols to design and develop calendars. Understand and interpret clinical trial agreements and sponsor budgets to develop site budgets for the protocol.
- Design and develop case report forms for clinical trial study protocols
- Develop a familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to utilize related functionalities in the design and development of calendars, budgets, financials and case report forms.
- Maintain high level quality and customer SLAs for all services.
- Provide input in process development and improvement.
- Assist in developing internal and customer facing documentation.
- Independently troubleshoot customer reported issues.
- Train fellow team members. Work closely with reporting manager to complete daily/ weekly calendars, budgets, financials and/or case report forms design in order to meet with pre-determined quality criteria
- Participate in customer interactions over the e-mail/telephonically to assimilate customer requirements and address those adequately in all services.
- Assist in managing team work/work load distribution by understanding and utilizing internal case management software and other reporting software to ensure that daily/weekly work assignments are appropriately tracked and completed
- Actively participate in team meetings and contribute meaningfully to discussions related to specific customer cases and/or protocols.
- Minimum qualification: Degree in Life sciences/related fields.
- 3+ years’ work experience in job areas such as:
- Clinical data management
- Clinical trial coordination at site
- Clinical research associate
- Records management
- Sound knowledge of clinical research methodology, industry regulations and Good Clinical Practice guidelines related to human research
- Expected to work independently, as well as in a team environment
- Excellent organizational and administrative abilities
- Ability to liaise with key stakeholders across the organization
- Familiarity with MS Office and various business software
Advarra Hiring Life Science Candidates. The possible interview Q & A to help you with:
1.Question: What qualifications do you possess that make you a strong candidate for the Research Associate III position at Advarra?
Answer: I hold a degree in Life Sciences, and I have over three years of work experience in various roles related to clinical research, including clinical trial coordination, clinical data management, and pharmacovigilance. My comprehensive understanding of clinical research methodology, industry regulations, and Good Clinical Practice guidelines further supports my qualifications for this role.
2.Question: Can you describe your experience with clinical trial budget development and site budgeting for protocols?
Answer: Certainly. I have a proven track record of interpreting clinical trial agreements and sponsor budgets to create site budgets aligned with the study protocols. This involves a meticulous review of trial agreements and protocol requirements to ensure accurate budgeting that meets both sponsor and site needs.
3.Question: How familiar are you with Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software, and how have you utilized them in your previous roles?
Answer: I am highly familiar with both CTMS and EDC software. In my previous positions, I have effectively utilized these systems to streamline the design and development of study calendars, budgets, financials, and case report forms. This proficiency has enabled me to enhance operational efficiency and maintain data accuracy.
4.Question: Can you provide an example of a challenging customer interaction you’ve experienced in your previous roles and how you resolved it?
Answer: In a previous role, I encountered a situation where a customer had specific requirements that seemed challenging to accommodate initially. However, through effective communication and problem-solving, I was able to find a solution that met the customer’s needs while still adhering to established protocols and guidelines. This experience showcased my ability to address complex customer demands while maintaining compliance.
5.Question: How do you manage your workload and ensure timely completion of tasks, especially when working on multiple projects simultaneously?
Answer: To manage my workload effectively, I rely on internal case management and reporting software. I prioritize tasks based on urgency and importance, ensuring that daily and weekly work assignments are tracked and completed in a timely manner. This approach helps me balance multiple projects efficiently and meet pre-determined quality criteria while collaborating with the team to ensure smooth workflow distribution.