Senior In-House CRA – Remote Clinical Trials & Compliance

Emmes Group; Rockville (MD); Remote; USD 70,000 - 100,000; Full time

Benefits offered by this job

Flexible PTO

Tuition Reimbursement

401(k) Plan

Work From Home (US)

Parental Leave

Casual Dress Code

Job summary

Emmes Group is seeking a Senior In-House Clinical Research Associate to support site management and monitoring of clinical studies from a remote location within the United States. The role demands 2–3 years of clinical research experience and a scientific degree, with proficiency in MS Office and strong organizational skills.

You will work under supervision, triage site questions, manage essential documents, and assist with IRB submissions, training, and data review.

Qualifications

• Bachelor's degree in科学 or directly applicable work experience preferred.
• 2–3 years of clinical research experience (CTA/CRA/study coordinator) required.
• Proficiency with MS Office and strong organizational skills.

Responsibilities

• Support site management and monitoring of clinical studies.
• Triage questions from site staff and coordinate meeting arrangements.
• Ensure regulatory compliance and handling of essential documents.
• Maintain site training records and assist in IRB/EC submissions.
• Update trial management systems with progress and metrics.
• Assist with audit preparation and issue resolution.
• Monitor data queries and assist with site recruitment tracking.

Skills

Attention to detail

Organization

Communication

Independent but team player

Critical thinking

Time management

Education

Bachelor's degree in science

Tools

MS Office Suite

Job description

Emmes Group is seeking a Senior In-House Clinical Research Associate to support site management and monitoring of clinical studies from a remote location within the United States. The role demands 2–3 years of clinical research experience and a scientific degree, with proficiency in MS Office and strong organizational skills.

You will work under supervision, triage site questions, manage essential documents, and assist with IRB submissions, training, and data review.