Senior In-House CRA — Remote Clinical Trials Leader

Emmes Group; Oregon; Hybrid; USD 70,000 - 95,000; Full time

Benefits offered by this job

Flexible time off

Tuition reimbursement

401k retirement plan

Work from home anywhere in the US

Maternity/Paternity leave

Casual dress code & work environment

Job summary

Emmes Group is seeking a Sr. In-House CRA to support site management and monitoring of clinical studies, ensuring adherence to protocol, SOPs, and regulatory requirements.

The role includes document maintenance, IRB submissions, and cross-functional coordination with project teams. The candidate should have 2–3 years of clinical research experience, strong MS Office skills, and a science degree, with knowledge of ICH guidelines and quality-oriented attention to detail.

Qualifications

• Bachelor's Degree in a scientific discipline preferred or directly applicable work experience
• 2-3 years of relevant clinical research experience
• Proficient with MS Office Suite
• Excellent computer and organizational skills
• Ability to work independently and cross-functionally with limited oversight
• Knowledgeable in clinical research operations and ICH guidelines
• Strong problem solving and communication skills

Responsibilities

• Assist with site management and monitoring of clinical studies
• Ensure trials are conducted, recorded, and reported per protocol and SOPs
• Maintain essential documents and review for completeness and regulatory compliance
• Submit IRB/EC submissions and track approvals
• Provide trial progress tracking and support junior staff
• Assist in audit preparation and issue resolution
• Coordinate with internal and site staff and manage training and recruitment logs

Skills

MS Office Suite proficiency

Attention to detail

Independent and team player

Strong communication skills

Education

Bachelor's Degree in Scientific discipline

Tools

MS Office Suite

Job description

Emmes Group is seeking a Sr. In-House CRA to support site management and monitoring of clinical studies, ensuring adherence to protocol, SOPs, and regulatory requirements.

The role includes document maintenance, IRB submissions, and cross-functional coordination with project teams. The candidate should have 2–3 years of clinical research experience, strong MS Office skills, and a science degree, with knowledge of ICH guidelines and quality-oriented attention to detail.