Join IQVIA as a Sr Clin Data Coordinator in Thane

IQVIA Hiring Sr Clin Data Coordinator – Thane: Unlock Your Career Potential

Introduction:

Embark on a rewarding career journey with IQVIA, a global leader in advanced analytics, technology solutions, and clinical research services. We are seeking passionate individuals to join our team as Sr Clin Data Coordinators in Thane, Maharashtra, India. Dive into the world of clinical data management and contribute to groundbreaking advancements in healthcare.

Company Overview:

IQVIA is at the forefront of transforming the life sciences industry through innovative solutions and cutting-edge research. With a rich legacy of pushing the boundaries of human and data science, we are committed to creating a healthier world. Founded on the principles of excellence and integrity, IQVIA fosters a culture of collaboration, innovation, and impact.

Company Vacancies List:

Position Title: Sr Clin Data Coordinator

Company Name: IQVIA

Salary: Competitive, commensurate with experience

Company Address: Thane, Maharashtra, India

Department: Clinical Data Management

Employment Type: Full-time

Role Category: Data Management

Educational Background Required: Bachelor’s Degree in Health, Clinical, Biological Sciences, or related field

Key Skills: Clinical trials experience, medical terminology, organizational skills

Job Description:

Join our dynamic team as a Sr Clin Data Coordinator and take on the following responsibilities:

Responsibilities:

• Manage project timelines and quality through the full data management study life-cycle.
• Determine resource needs and identify out-of-scope work.
• Perform comprehensive data management tasks including data review and resolution of data clarifications.
• Independently bring project solutions to the CDM team and solve issues through the global issue escalation/communication plan.
• Develop and maintain effective working relationships with coworkers, managers, and clients.

Qualifications:

• Bachelor’s Degree in Health, Clinical, Biological Sciences, or related field required.
• 1 year of clinical trials experience in a function similar to data management.
• Good understanding of the clinical drug development process.
• Background in medical terminology, pharmacology, anatomy, and physiology.
• Excellent organizational, communication, and data management skills.

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