Clinical Data Associate

Serve in support-level capacity on a Clinical Data Management team to provide efficient, quality data entry, query resolution, and administrative services that meet customer needs.

Responsible for clinical trials data entry.

Responsible for the administration of volunteer logistics.

Assisting with clinical trial administrative duties.

Responsible for assisting at sponsor monitoring visits.

Assist with database updating / other data related activities.

Responsible for archiving duties.

Requirements:

• High School Diploma or equivalent
• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
• Written and verbal communication skills including good command of English language.

• High level of autonomy.
• Global exposure
• Variety of therapeutic areas
• Collaborative and supportive team environment
• Access to cutting-edge and innovative, in-house technology
• Excellent career development and progression opportunities
• Work-Life Balance, with a strong focus on a positive well-being.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.