Research Associate I Job in Bengaluru | Clinical Research
Are you passionate about clinical research and looking to kickstart your career as a Research Associate? Join our dynamic team in Bengaluru, India, and be part of groundbreaking clinical trials that make a difference. We are currently seeking a Research Associate I to join our dedicated team.
Vacancies List:
- Position Title: Research Associate I
- Company Name: Advarra
- Salary: Competitive
- Company Address: Bengaluru – IND
Detailed Job Description:
Role: Research Associate I
Industry Type: Research
Department: Clinical Research
Employment Type: Full-Time
Role Category: Entry Level
Primary Duties and Responsibilities:
- Protocol Design: Understand and interpret clinical trial study protocols to design and develop calendars.
- Budget Development: Interpret clinical trial agreements and sponsor budgets to develop site budgets for the protocol.
- Form Creation: Design and develop case report forms for clinical trial study protocols.
- Software Utilization: Develop familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to utilize related functionalities in designing calendars, budgets, financials, and case report forms.
- Collaboration: Work closely with the reporting manager to complete daily/weekly calendars, budgets, financials, and case report forms to meet pre-determined quality criteria.
- Workflow Management: Understand and utilize internal case management software and other reporting tools to ensure proper tracking and completion of daily/weekly work assignments.
- Team Participation: Actively participate in team meetings and contribute meaningfully to discussions related to specific customer cases and/or protocols.
Position Requirements:
- Knowledge of clinical research methodology, industry regulations, and Good Clinical Practice guidelines related to human research.
- Ability to work independently and in a team environment.
- Strong organizational and administrative abilities.
- Familiarity with MS Office and various business software.
- Preferred: 0-1 year work experience in job areas such as clinical trial coordination, clinical data management, pharmacovigilance, or records management.
How to Apply:
If you are ready to embark on a fulfilling career journey as a Research Associate I and meet the requirements mentioned above,