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Work/Life Balance

Time management

challenging projects

Insurance

IQVIA, a global leader in healthcare data analytics and technology, is on the lookout for Clinical Data Management professionals to help drive innovations in the healthcare sector. With a focus on delivering groundbreaking solutions to the pharmaceutical, biotechnology, and medical device industries, IQVIA is advancing the future of healthcare and improving patient outcomes worldwide.

Responsibilities of the Job

As a Clinical Data Management Professional at IQVIA, you will be responsible for managing clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. Key responsibilities include:

  • Study Management: Overseeing the end-to-end lifecycle of clinical studies, including startup, conduct, and closeout.
  • Data Management: Hands-on involvement with data reconciliation, query management, and database locking to ensure high-quality data.
  • Rave EDC Proficiency: Utilizing Rave Electronic Data Capture (EDC) systems for clinical data collection, monitoring, and reporting.
  • User Acceptance Testing (UAT): Conducting UAT to ensure the systems meet study requirements and provide a smooth data flow.
  • Collaborative Support: Coordinating with cross-functional teams to ensure seamless data management throughout the clinical trial process.

Required Qualifications and Experience

To be eligible for this exciting opportunity, you need the following qualifications and experience:

  • Industry Experience: 2-5 years of experience in Clinical Core Data Management.
  • End-to-End Clinical Data Management: Proven experience in managing all phases of clinical trials, from study startup through to closeout.
  • Rave EDC Expertise: Hands-on experience with Rave EDC systems is a must.
  • Data Reconciliation & Query Management: Experience in data reconciliation, managing queries, and performing database lock activities.
  • Shift Work: Willingness to work in shifts is required to meet project deadlines and ensure timely data management.

Please note, experience from CRA, CRC, PV, Regulatory, QC, or Safety roles will not be considered for this requirement. Only candidates with relevant experience in Core Clinical Data Management will be eligible for this position.

Key Skills Required

Successful candidates for this role should possess the following skills:

  • Strong knowledge of clinical data management processes and industry best practices.
  • In-depth understanding of clinical trial data and regulatory requirements.
  • Proficiency with Rave EDC systems and other clinical data management tools.
  • Excellent problem-solving and analytical skills.
  • Strong communication and teamwork abilities, with a collaborative approach to working in a global team environment.
  • Attention to detail and the ability to manage multiple tasks effectively.

How to Apply

If you meet the required qualifications and are passionate about advancing healthcare innovation, we encourage you to apply! Simply send your CV to jinto.jacobc@iqvia.com and take the first step toward a fulfilling career with IQVIA.

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