Clinical Research Associate – IQVIA Careers
IQVIA, a global leader in clinical research and healthcare analytics, is seeking a Clinical Research Associate (CRA) – Sponsor Dedicated for a full-time, field-based role in Parsippany, New Jersey. The CRA will oversee site monitoring and management activities to ensure compliance with clinical trial protocols, regulatory guidelines, and sponsor requirements. This Clinical Research Associate Role at IQVIA Careers is ideal for professionals passionate about clinical research, regulatory excellence, and advancing innovative medical solutions.
Job Details:
- Position Title: Clinical Research Associate – Sponsor Dedicated
- Job ID: R1507163
- Location: Parsippany, New Jersey (Field-based)
- Employment Type: Full-time
- Department: Clinical Research / Site Management
- Pay Range: $71,900 – $189,000 (annualized, depending on qualifications and experience)
- Additional Locations: Multiple locations available
About the Company:
IQVIA is a leading global provider of clinical research services, advanced analytics, and technology solutions for the life sciences industry. With a mission to improve healthcare outcomes worldwide, IQVIA partners with pharmaceutical and biotech companies to accelerate clinical development and bring innovative therapies to patients faster. The company operates in over 100 countries and is recognized for driving transformative healthcare insights through data science and technology.
Educational Requirements:
- Required: Bachelor’s degree in a scientific discipline or healthcare-related field
- Preferred: Prior CRA training program or monitoring experience
- Equivalent: Relevant education, training, or experience may be accepted instead of a degree
Key Responsibilities of the Clinical Research Associate Role:
- In this Clinical Research Jobs, you have to conduct site visits (selection, initiation, monitoring, and close-out) in compliance with GCP and ICH guidelines
- Manage subject recruitment and study progress to meet project timelines
- Administer study protocol training and maintain communication with assigned sites
- Evaluate site performance, data integrity, and adherence to regulatory standards
- Track submissions, approvals, and data management activities
- Maintain accurate documentation for Trial Master File (TMF) and Investigator Site File (ISF)
- Collaborate with project teams to resolve issues and enhance site performance
- Support the development and management of recruitment plans and site finances, where applicable
Skills Required for the Clinical Research Associate Role:
- Strong knowledge of GCP, ICH, and clinical research regulations
- Excellent written and verbal communication skills
- Proficiency in Microsoft Word, Excel, PowerPoint, and digital tools (iPhone/iPad)
- Good therapeutic area understanding
- Strong organizational, analytical, and problem-solving skills
- Time and financial management abilities
- Ability to build and maintain professional relationships with study sites and teams
How to Apply?
Interested candidates for the Clinical Research Jobs can apply online through IQVIA’s official career portal. Ensure that your resume, academic qualifications, and relevant certifications are included when applying.
