Senior Clinical Research Associate: Protocol IRB Support

Global Solutions Network Inc; Bethesda (MD); On-site; USD 78,000 - 149,000; Full time

Benefits offered by this job

Medical, Dental, & Vision Coverage

Paid Time Off and Paid Holidays

401K/Profit Sharing Plan

Flexible Spending Accounts (Healthcare

Dependent Care)

Pretax Parking & Transportation Plan

Short-Term & Long-Term Disability

Life & AD&D Insurance

Professional Development/Education

Employee Referral Bonuses

Employee Discount Program

Merit Bonuses

Employee Assistance Program

Travel Assistance Program

Job summary

Global Solutions Network, Inc. (GSN) is seeking a Senior Research Associate (Clinical) to support NIH at the National Institutes of Health in Bethesda, Maryland. The role involves assisting researchers with proposals, protocol development, and regulatory documentation to ensure smooth study conduct.

The position is full-time and long-term, with a competitive salary and comprehensive benefits. A Master's degree and familiarity with regulatory processes are required.

Qualifications

• Master's degree in a related field.
• CITI certification.
• Familiarity with Electronic Data Capture Systems.

Responsibilities

• Assist researchers develop internal proposals, abstracts, posters and manuscripts.
• Assist protocol documentation including schemas, calendars and teaching aids.
• Assist IRB and regulatory documentation throughout the study life cycle.
• Maintain study documentation including investigator qualifications, trial logs and safety reports.
• Prepare and submit protocol actions for NIH Protocol Tracking and Management System.

Skills

Regulatory liaison

Training site staff

Coordinating meetings

Clinical trial work

Education

Master's degree in a related field

CITI certification

Tools

Electronic Data Capture Systems

Job description

Global Solutions Network, Inc. (GSN) is seeking a Senior Research Associate (Clinical) to support NIH at the National Institutes of Health in Bethesda, Maryland. The role involves assisting researchers with proposals, protocol development, and regulatory documentation to ensure smooth study conduct.

The position is full-time and long-term, with a competitive salary and comprehensive benefits. A Master's degree and familiarity with regulatory processes are required.