Impactful Clinical Research Data & Regulatory Specialist

Deborah Heart and Lung Center; Pemberton Township (NJ); Sur place; USD 23 000 - 32 000; Plein temps

Avantages offerts par ce poste

Healthcare coverage

Paid time off

401K matching

Tuition assistance

Free parking

Résumé du poste

Deborah Heart and Lung Center in New Jersey seeks a Clinical Research Data and Regulatory Coordinator to manage IRB submissions, data collection, and regulatory compliance under the Clinical Research Director.

This entry-level role requires attention to deadlines, teamwork, and communication with sponsors and investigators; cardiovascular experience is preferred.

The position offers a competitive benefits package and a path to grow within the clinical research program.

Qualifications

• Associates degree in science required.
• 1–2 years of medical clinical experience required.
• Bachelor’s degree in related field preferred.
• HHS/IRB training or GCP certification required within two weeks of hire.

Responsabilités

• Prepare IRB submissions and amendments.
• Abstract data and collect protocol-specific information.
• Maintain regulatory documentation and ensure compliance.
• Coordinate communication with sponsors and study teams.
• Monitor study progress and generate data reports.

Connaissances

Regulatory submissions

Data management

Medical terminology

Multitasking

English fluency

Microsoft Office

Formation

Associates degree in science

Bachelor’s degree (preferred)

Outils

iMedidata

REDCap

eTMF

Description du poste

Deborah Heart and Lung Center in New Jersey seeks a Clinical Research Data and Regulatory Coordinator to manage IRB submissions, data collection, and regulatory compliance under the Clinical Research Director.

This entry-level role requires attention to deadlines, teamwork, and communication with sponsors and investigators; cardiovascular experience is preferred.

The position offers a competitive benefits package and a path to grow within the clinical research program.