Regional Clinical Trial Leader I

The Emmes Company, LLC; Rockville (MD); In loco; USD 90.000 - 120.000; Tempo pieno

Descrizione del lavoro

The Emmes Group is seeking a Clinical Trial Manager I to lead regional operational activities across studies, ensuring timelines and quality at clinical sites. You will supervise the monitoring team and deliverables, coordinating with project leadership and clients to keep trials on track.

Ideal candidates have 4–6 years of clinical research experience, strong mentoring skills, and a solid foundation in study plans, SOPs, and regulatory requirements.

Competenze

• Bachelor's degree in 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.
• Excellent organizational, analytical and communication skills are required.

Mansioni

• Leads operational activities for a study or group of studies at a regional level.
• Mentors CRAs, in-house CRAs, and site management staff on assigned projects.
• Coordinates study implementation and oversees clinical operations activities per SOPs and study plans.
• Provides forecast projections to GPM and tracks team workload.
• Maintains relationships with clients, vendors and internal teams; communicates status of activities.
• Ensures study timelines and deliverables meet governance and regulatory requirements.

Conoscenze

Team building

Interpersonal skills

Organizational skills

Analytical skills

Verbal communication

Written communication

Formazione

Bachelor's degree in science-related field

Master's degree in science-related field

Strumenti

MS Office Suite

Descrizione del lavoro

The Emmes Group is seeking a Clinical Trial Manager I to lead regional operational activities across studies, ensuring timelines and quality at clinical sites. You will supervise the monitoring team and deliverables, coordinating with project leadership and clients to keep trials on track.

Ideal candidates have 4–6 years of clinical research experience, strong mentoring skills, and a solid foundation in study plans, SOPs, and regulatory requirements.