Regulatory Affairs Coordinator: Clinical Trials

Virtua Health; Moorestown Township (NJ); Hybrid; USD 36,000 - 54,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) plan

Paid time off

Tuition assistance

Employee assistance program

Job summary

Virtua Health in Moorestown, NJ seeks a Regulatory Affairs Specialist to coordinate regulatory activities for clinical trials. You will prepare IRB submissions, maintain study documents, and support audits across multiple sites.

The role requires at least 3 years of regulatory support in clinical research, excellent organizational and communication skills, and an Associate degree (Bachelor's preferred). Hybrid onsite work with standard business hours.

Qualifications

• Minimum of 3 years supporting regulatory activities in clinical research.
• Ability to function independently with strong organizational skills.
• Excellent communication and interpersonal skills.

Responsibilities

• Prepare and submit regulatory documents for IRB and central IRBs.
• Maintain regulatory study documents and SOPs; participate in audits.
• Coordinate study activations and regulatory training.
• Monitor regulatory training and site communications.

Skills

Regulatory coordination

IRB submissions

Clinical research

Documentation management

Communication skills

Education

Associate degree

Bachelor's degree

Job description

Virtua Health in Moorestown, NJ seeks a Regulatory Affairs Specialist to coordinate regulatory activities for clinical trials. You will prepare IRB submissions, maintain study documents, and support audits across multiple sites.

The role requires at least 3 years of regulatory support in clinical research, excellent organizational and communication skills, and an Associate degree (Bachelor's preferred). Hybrid onsite work with standard business hours.