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ICF Specialist at IQVIA - ApplyBlast

ICF Specialist

IQVIA

7 days ago

3.8 on Glassdoor

Sofia, Bulgaria

Onsite

Full Time

Medior

0 applicants

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About this role

The ICF Specialist reviews, coordinates, and finalizes Global Informed Consent Form templates for sponsor clinical studies under the guidance of Global Clinical Study Support management. The role may also involve performing country-level Site Activation activities, maintaining centralized systems, and ensuring compliance with applicable regulations and standard operating procedures. This position serves as a key contact for investigative sites and project teams to support regulatory document preparation and timeline adherence.

Responsibilities

Review and finalize Global Informed Consent Form templates for clinical studies
Coordinate site activation activities and manage regulatory document approvals
Track progress of ICF reviews and resolve RFIs and ethics queries

Skills

About IQVIA

iqvia.com

Headquarters

Durham, North Carolina, United States

Company Size

10001+ employees

Founded

2016

View Profile

IQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.