Clinical Trial Manager I — Remote

Emmes Group; Rockville (MD); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Flexible Approved Time Off

Tuition Reimbursement

401k Retirement Plan

Work From Home Anywhere in the US

Maternal/Paternal Leave

Casual Dress Code & Work Environment

Job summary

Emmes Group is seeking a Clinical Trial Manager I to lead regional operational activities and oversee CRA teams across studies. You will drive study timelines, monitor site performance, and ensure adherence to SOPs and client requirements.

The role emphasizes mentorship, cross-functional collaboration, and delivering high-quality data while maintaining compliance with regulatory standards. Emmes Group offers a collaborative, innovative environment in which to advance global health impact.

Qualifications

• Bachelor's degree in a science-related field is required.
• 4–6 years of relevant clinical research experience is required.
• 1–3 years of CRA or clinical operations coordinating experience is required.
• Strong team leadership, organizational and communication skills are required.

Responsibilities

• Lead operational activities for a study or group of studies at a regional level.
• Oversee the monitoring team and deliverables, including the clinical monitoring plan.
• Ensure study timelines are met and communicated to the Project Leader/Global Clinical Project Manager.
• Mentor CRAs and site staff on assigned projects.
• Coordinate study implementation with SOPs and client guidelines.
• Develop and review study plans, templates, and monitoring documents.
• Maintain site documentation currency and ethics approvals.

Skills

Team leadership

Interpersonal skills

Organizational skills

Communication skills

Prioritization

Independent work

MS Office

Problem solving

Clinical research operations

Education

Bachelor's Degree in science

Master's Degree in science

Job description

Emmes Group is seeking a Clinical Trial Manager I to lead regional operational activities and oversee CRA teams across studies. You will drive study timelines, monitor site performance, and ensure adherence to SOPs and client requirements.

The role emphasizes mentorship, cross-functional collaboration, and delivering high-quality data while maintaining compliance with regulatory standards. Emmes Group offers a collaborative, innovative environment in which to advance global health impact.