On-site Clinical Research Data & Regulatory Specialist

Deborah; Pemberton Township (NJ); Hybrid; USD 23,000 - 32,000; Full time

Benefits offered by this job

Healthcare coverage

Paid time-off

401K matching contribution

Tuition assistance

Short and long term disability

Life insurance

Meal discount

Dependent care subsidy

Adoption assistance

Free parking

Job summary

Deborah is seeking a Clinical Research Data and Regulatory Coordinator on-site at Browns Mills, NJ. The role supports IRB submissions, data management, and regulatory compliance under the supervision of the Clinical Research Director and senior staff.

Responsibilities include preparing regulatory documents, collecting study data, coordinating with investigators, sponsors, and sites, and ensuring adherence to protocol and federal regulations.

Qualifications

• Associates degree in science or related field required.
• Certified or cardiovascular research experience preferred.
• Ability to meet deadlines and manage multiple studies.

Responsibilities

• Prepare and maintain IRB submissions and regulatory documents.
• Collect protocol-specific information from investigators and sites.
• Coordinate data collection and regulatory activities across trial sites.
• Ensure compliance with protocol, IRB, and regulations.

Skills

Data management

Regulatory submissions

IRB submissions

Communication skills

MS Office (Outlook, Word, Excel, Power

Education

Associates degree in science

Bachelor’s degree (preferred)

Tools

iMedidata

REDCap

MS Outlook

MS Word

MS Excel

MS PowerPoint

Job description

Deborah is seeking a Clinical Research Data and Regulatory Coordinator on-site at Browns Mills, NJ. The role supports IRB submissions, data management, and regulatory compliance under the supervision of the Clinical Research Director and senior staff.

Responsibilities include preparing regulatory documents, collecting study data, coordinating with investigators, sponsors, and sites, and ensuring adherence to protocol and federal regulations.