Remote Oncology Clinical Trial Manager – Lead Trials

BioCT Innovation Commons; Ridgefield (CT); A distancia; USD 128.000 - 248.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical insurance

Dental & Vision

Retirement plan

Paid time off

Discretionary bonus

Relocation assistance

Descripción de la vacante

BioCT Innovation Commons is seeking a Clinical Trial Manager to lead late-phase oncology trials in the US region. You will oversee trial setup, execution, and closeout with a focus on regulatory compliance and patient/site engagement.

The role requires coordinating with internal teams and external sites, managing budgets, and ensuring timely data delivery and reporting to stakeholders. You will play a key part in driving trial success and site performance across the program.

Formación

• Bachelor's degree in life sciences or related field with minimum six (6) years of clinical research experience.
• Master's degree or PharmD plus minimum of four (4) years of clinical research experience.
• PharmD with completion of a 2-year clinical research fellowship.
• PhD or MD plus minimum of two (2) years of clinical research experience.

Responsabilidades

• Oversee trial setup, conduct, and closeout in compliance with GCP-ICH and local/global regulations.
• Provide leadership to the US trial team and coordinate with internal/external stakeholders.
• Develop country-level engagement plans, recruitment strategies, and risk mitigation.
• Ensure timely data delivery, TMF archival, and regulatory submissions.

Conocimientos

Leadership

Oncology trials

Project management

Cross-functional collaboration

Communication

Educación

Bachelor's degree in Life Sciences

Master’s degree or PharmD

PharmD with 2-year clinical research fellowship

PhD or MD with 2+ years clinical research

Descripción del empleo

BioCT Innovation Commons is seeking a Clinical Trial Manager to lead late-phase oncology trials in the US region. You will oversee trial setup, execution, and closeout with a focus on regulatory compliance and patient/site engagement.

The role requires coordinating with internal teams and external sites, managing budgets, and ensuring timely data delivery and reporting to stakeholders. You will play a key part in driving trial success and site performance across the program.