Remote Clinical Trial Manager I – Lead Site Operations

Emmes; Rockville (MD); Remote; USD 90.000 - 120.000; Vollzeit

Benefits dieser Stelle

Flexible Approved Time Off

Tuition Reimbursement

401k Retirement Plan

Work From Home Anywhere in the US

Maternal/Paternal Leave

Casual Dress Code & Work Environment

Zusammenfassung

Emmes is seeking a Clinical Trial Manager I to lead regional operational activities and monitor study progress. You will oversee the monitoring team, ensure timelines, and mentor CRAs and site staff across projects.

The role emphasizes client communication, SOP adherence, and cross-functional collaboration from a remote US-based setting. Ideal candidates will have a science background, 4–6 years in clinical research, and 1–3 years in CRA/clinical operations roles, with strong teamwork and

Qualifikationen

• Bachelor's degree in a science-related field is required.
• Master's degree in science is preferred.
• 4-6 years of relevant clinical research experience required.
• 1-3 years experience as CRA or in a clinical operations coordinating role required.
• Excellent team-building and interpersonal skills emphasized.
• Strong organizational and analytical capabilities highlighted.

Aufgaben

• Oversee the monitoring team and deliverables for regional studies.
• Lead operational activities and ensure timelines are met.
• Mentor CRAs and site management staff on projects.
• Coordinate study tasks according to SOPs and client requirements.
• Maintain client, vendor, and internal stakeholder relationships.
• Monitor study plans, CMP, MOP, and other templates for compliance.
• Track site performance metrics and study progress.
• Communicate status updates to study leaders and teams.

Kenntnisse

Team leadership

Organization

Communication

Independent work

MS Office

Attention to detail

Prioritization

Analytical skills

Ausbildung

Bachelor's degree in science

Master's degree (preferred)

Jobbeschreibung

Emmes is seeking a Clinical Trial Manager I to lead regional operational activities and monitor study progress. You will oversee the monitoring team, ensure timelines, and mentor CRAs and site staff across projects.

The role emphasizes client communication, SOP adherence, and cross-functional collaboration from a remote US-based setting. Ideal candidates will have a science background, 4–6 years in clinical research, and 1–3 years in CRA/clinical operations roles, with strong teamwork and