Senior Clinical Protocol Coordinator (Research Associate)

Axle; Rockville (MD); Hybrid; USD 145,000 - 153,000; Full time

Benefits offered by this job

100% Medical, Dental & Vision Coverage

Paid Time Off and Holidays

401K match up to 5%

Educational Benefits for Career Growth

Employee Referral Bonus

Flexible Spending Accounts: Healthcare

Parking Reimbursement Account

Dependent Care Assistant Program

Transportation Reimbursement Account

Job summary

Axle, a bioscience and IT company, is seeking a Senior Research Associate (Clinical Protocol Coordinator) to support the NIH Clinical Center's Department of Perioperative Medicine in Bethesda, MD. This full-time role involves protocol development, regulatory submissions, data management, and staff training.

The position requires a Master’s degree, CITI certification, and experience with clinical trials. It is based at NIH Bethesda with telework eligibility and a Monday–Friday schedule.

Qualifications

• Master's degree in General Medical and Health Services or related field.
• CITI certification.
• Experience with regulatory submission processes and IRB documentation.

Responsibilities

• Assist researchers with protocol development and review of trial documents.
• Maintain trial-related documentation and study databases.
• Collect and submit regulatory documents to IRB and regulatory bodies.
• Support participant recruitment and scheduling; train staff on protocol submissions.
• Train investigators and staff on protocol submission processes.

Skills

Liaising with regulatory authorities

Training clinical trial site staff

Coordinating project meetings

Previous clinical trial work

Education

Master's degree

Tools

Electronic Data Capture System

Job description

Axle, a bioscience and IT company, is seeking a Senior Research Associate (Clinical Protocol Coordinator) to support the NIH Clinical Center's Department of Perioperative Medicine in Bethesda, MD. This full-time role involves protocol development, regulatory submissions, data management, and staff training.

The position requires a Master’s degree, CITI certification, and experience with clinical trials. It is based at NIH Bethesda with telework eligibility and a Monday–Friday schedule.