Associate Trainee Clinical Data Coordinator

Roles & Responsibilities
• Perform roles such as Data Entry Associate, File Room Associate, Scanning Associate, or Indexing Associate
• Process, log, scan, index, and track clinical study documents as per CRF Tracking and Data Entry Guidelines
• Enter clinical trial data accurately within defined timelines
• Maintain Clinical Data Management (CDM) study files
• Follow core operating procedures (SOPs) and working instructions
• Meet productivity, quality, and compliance objectives
• Collaborate effectively with CDM team members and study stakeholders

Qualification
• High School Diploma or equivalent (mandatory)
• Equivalent combination of education, training, and experience may be considered

Experience
• Freshers and early-career professionals are eligible

Skills
• Strong attention to detail and accuracy
• Good organizational and communication skills
• Excellent computer proficiency
• Ability to follow processes and meet deadlines
• Team-oriented mindset with the ability to work with coworkers, managers, and clients

About the Organization
IQVIA – A global leader in clinical research, healthcare analytics, and technology solutions, offering strong career entry opportunities in Clinical Data Management and global clinical operations.