Remote Phase I Trial Coordinator

Fortrea; Durham (NC); À distance; USD 39 000 - 48 000; Plein temps

Avantages offerts par ce poste

Résumé du poste

Fortrea is seeking a Project Coordinator I to join our clinical operations team. This remote role supports Phase I studies from the United States, coordinating activities, maintaining documents, and helping keep trials on track and audit-ready.

You will work with experienced project managers and cross-functional teams, manage CTMS and eTMF workflows, track timelines, and mentor junior staff. A life sciences degree and 2–3 years of clinical research experience are preferred.

Qualifications

• Degree in life sciences or related field (or equivalent experience).
• 2–3 years of clinical research experience.
• Experience supporting project management or study coordination.
• GCP/ICH guidelines and clinical trial processes knowledge.
• Strong organizational, communication, and problem-solving skills.

Responsabilités

• Coordinate and support delivery of Phase I clinical trials, including external site studies.
• Develop and maintain key study documents (project plans, communication plans, risk registers).
• Track timelines, milestones, and study progress to ensure successful execution.
• Lead and support study meetings, including agendas, minutes, and follow-up actions.
• Manage systems such as CTMS and eTMF, ensuring accuracy and compliance.
• Act as a key point of contact for internal teams and external sites.
• Support feasibility, start-up activities, and vendor coordination.
• Contribute to continuous improvement initiatives and help mentor junior team members.

Connaissances

Project coordination

GCP/ICH knowledge

Organizational skills

Communication skills

Problem-solving

Formation

Life sciences degree

Outils

CTMS

eTMF

Description du poste

Fortrea is seeking a Project Coordinator I to join our clinical operations team. This remote role supports Phase I studies from the United States, coordinating activities, maintaining documents, and helping keep trials on track and audit-ready.

You will work with experienced project managers and cross-functional teams, manage CTMS and eTMF workflows, track timelines, and mentor junior staff. A life sciences degree and 2–3 years of clinical research experience are preferred.