At Advarra, we are passionate about making a difference in the world of clinical research and advancing human health. With a rich history rooted in ethical review services combined with innovative technology solutions and deep industry expertise, we are at the forefront of industry change. A market leader and pioneer, Advarra breaks the silos that impede clinical research, aligning patients, sites, sponsors, and CROs in a connected ecosystem to accelerate trials.
- Vacancy details:
- Department: Research Associate
- Experienced: 0-1 year
- Salary:  ₹Not Disclosed
Job Description: Greetings from Advarra pvt ltd..!!
Important Details :
- Location: Bengaluru, India.
- Post of date:19/10/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
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Job Duties & 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.
Work closely with reporting manager to complete daily/ weekly calendars, budgets, financials and/or case report forms design to meet with pre-determined quality criteria.
Understand and utilize 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.
Location
This role is open to candidates working remotely or hybrid in Bengaluru, India.
Basic Qualifications
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.
Good organizational and administrative abilities
Familiarity with MS Office and various business software
Preferred Qualifications
Preferred: 0-1 year work experience in job areas such as:
Clinical trial coordinator at site
Clinical data management
Pharmacovigilance
Records management
Physical and Mental Requirements
- Sit or stand for extended periods of time at stationary workstation
- Regularly carry, raise, and lower objects of up to 10 Lbs.
- Learn and comprehend basic instructions
- Focus and attention to tasks and responsibilities
- Verbal communication; listening and understanding, responding, and speaking
Advarra is an equal opportunity employer that is committed to diversity, equity and inclusion and providing a workplace that is free from discrimination and harassment of any kind based on race, color, religion, creed, sex (including pregnancy, childbirth, and related medical conditions, sexual orientation, and gender identity), national origin, age, disability or genetic information or any other status or characteristic protected by central, state, or local law. Advarra provides equal employment opportunity to all individuals regardless of these protected characteristics. Further, Advarra takes affirmative action to ensure that applicants and employees are treated without regard to any of these protected characteristics in all terms and conditions of employment, including, but not limited to, hiring, training, promotion, discipline, compensation, benefits, and separation from employment.
