[FRESHER] Advarra Hiring for TEMP Research Consultant- apply Now

[FRESHER] Advarra Hiring for TEMP Research Consultant- apply Now

Advarra, Inc. offers comprehensive solutions for compliance with research. The company offers clinical trial sponsors, CROs, hospital systems, academic medical institutions, and investigators institutional review board (IRB), institutional biosafety committee (IBC), and research compliance services.

Position Name : TEMP Research Consultant

Organization : Advarra

Qualification: N/A

Experience: 0-1 year

Salary: N/A

Location : Bengaluru

Job Title: TEMP Research Consultant

Job Category: Research

Requisition Number: TEMPR002873

Employment Type: Full-Time

Work Location: Hybrid (Bengaluru, IND)

Job Description

Primary Duties and Responsibilities:

  • Understand and interpret clinical trial study protocols to design and develop calendars.
  • 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 familiarity with Advarra’s Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software to utilize related functionalities.
  • Collaborate closely with the reporting manager to complete daily/weekly calendars, budgets, financials, and/or case report forms, ensuring they meet pre-determined quality criteria.
  • Use internal case management and reporting software to ensure 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.

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.
  • Good organizational and administrative skills.
  • Familiarity with MS Office and various business software.
  • Preferred: 0-1 year work experience in areas such as:
  • Clinical trial coordination at site
  • Clinical data management
  • Pharmacovigilance
  • Records management

Key Personal Attributes:

  • Highly personable nature that fosters teamwork.
  • Excellent communication skills (oral and written).
  • High energy and a positive attitude towards working in a culturally diverse environment.
  • Passion for ensuring outstanding customer support with a solutions-oriented attitude.
  • Proactive and takes ownership of all tasks from start to finish.

Working Hours:

  • Monday-Friday, 9:00 a.m. to 6:00 p.m
  • 3-month contract

Physical and Mental Requirements

  • Ability to sit or stand for extended periods at a stationary workstation.
  • Occasionally lift and/or move up to 25 pounds.
  • Specific vision abilities required: close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
  • Regular oral/written interaction with clients, team members, and management.

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