Remote Clinical Project Manager II: Trial Delivery

Symbio; United States; Remoto; USD 80.000 - 120.000; Tempo pieno

Descrizione del lavoro

Symbio is hiring an Associate Clinical Project Manager II for a fully remote role with occasional travel. You will provide project management support on assigned clinical trials, coordinating cross-functional study teams, maintaining trial documentation, and tracking progress and risks.

You will engage with sponsors, investigative sites, and internal stakeholders to ensure smooth trial execution. The ideal candidate has 2+ years of experience in clinical project management or pharmaceutical/ CRO

Competenze

• Bachelor’s degree in a scientific discipline or related field.
• 2+ years of experience as Associate Clinical Project Manager I or similar clinical trial management background.
• Working knowledge of GCP, ICH guidelines, and clinical trial regulations.
• Demonstrated scientific/medical understanding and familiarity with clinical research terms.
• Excellent organizational, analytical, problem-solving, and communication skills with ability to manage multiple priorities.

Mansioni

• Coordinate cross-functional teams to support trial execution and monitor progress, risks, and KPIs.
• Develop, review, and maintain TMF records, training materials, meeting agendas, and study reports.
• Collaborate with study sites and sponsors to support recruitment and escalation of issues.
• Assist investigator meetings, monitor visit reports, invoice review, and overall study operations management.
• Provide administrative and PM support as a key point of contact for stakeholders.

Conoscenze

Cross-functional coordination

Communication

Organizational skills

Analytical skills

Independent & collaborative work

Formazione

Bachelor's degree in a scientific discipline

Strumenti

Microsoft Office

Descrizione del lavoro

Symbio is hiring an Associate Clinical Project Manager II for a fully remote role with occasional travel. You will provide project management support on assigned clinical trials, coordinating cross-functional study teams, maintaining trial documentation, and tracking progress and risks.

You will engage with sponsors, investigative sites, and internal stakeholders to ensure smooth trial execution. The ideal candidate has 2+ years of experience in clinical project management or pharmaceutical/ CRO