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IQVIA Recruitment for Regulatory Start-Up Specialist

IQVIA Recruitment for Regulatory Start-Up Specialist

IQVIA Hiring for Regulatory Start-Up Specialist

Are you ready to advance your career in clinical research and regulatory affairs? IQVIA, a global leader in healthcare intelligence, is seeking skilled professionals to join their team as Regulatory Start-Up Specialists in Mumbai and Bangalore.

Job Overview

The Regulatory Start-Up Specialist at IQVIA plays a pivotal role in facilitating clinical research processes by ensuring compliance with regulatory requirements. This position, which requires site activation and regulatory documentation expertise, offers a rewarding career for professionals passionate about healthcare and clinical innovation.

Key Responsibilities

As a Regulatory Start-Up Specialist at IQVIA, your role will include:

  • Acting as the Single Point of Contact (SPOC) for investigative sites, Site Activation Managers (SAMs), and project teams.
  • Managing start-up and site activation activities in adherence to ICH-GCP standards, local regulatory guidelines, and company SOPs.
  • Preparing, reviewing, and maintaining site regulatory documents for accuracy and completeness.
  • Updating internal systems, databases, and trackers with project-specific information.
  • Tracking progress on regulatory submissions and contractual agreements to ensure timely approvals.
  • Providing local expertise to project teams during timeline planning and execution.
  • Coordinating with sponsors and internal stakeholders on specific regulatory initiatives.
IQVIA Recruitment for Regulatory Start-Up Specialist
IQVIA Recruitment for Regulatory Start-Up Specialist

Qualifications

To excel in this role, candidates must meet the following qualifications:

  • Education: Bachelor’s degree in Life Sciences, Clinical Research, Pharmacy, or related fields.
  • Experience: 1-3 years in clinical research, regulatory affairs, or site activation.
  • Skills:
    • Familiarity with ICH-GCP guidelines and local regulatory requirements.
    • Proficiency in tracking tools, databases, and documentation software.
    • Strong organizational and problem-solving abilities.
    • Excellent verbal and written communication skills.

H4: Job Location

The position is available in the cities of Mumbai and Bangalore

H2: How to Apply

Interested candidates can apply directly through the official LinkedIn posting. To apply, simply click on the ‘Apply’ button and follow the instructions to submit your application. Ensure your resume highlights relevant experience and qualifications for a competitive edge.

Tagged as: EU Markets, Good Clinical Practice (GCP), Pharmacology

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