Clinical Trial Manager: Lead Study Delivery & Compliance

Linical; Województwo mazowieckie; On-site; PLN 140,000 - 190,000; Full time

Job summary

Linical is seeking a Clinical Trial Manager to oversee studies, develop project documents, manage budgets, and ensure metrics and timelines are met. You will lead and train CRAs, coordinate with PM, clients and study teams, and supervise third-party vendors.

Key responsibilities include site activation planning, regulatory submissions oversight, monitoring plan development, budget negotiation, and performance reviews. Requires 3+ years in clinical trial management and life science background.

Qualifications

• Life Science degree or nursing background.
• Minimum of three years of clinical trial management experience.
• Experience leading CRAs and managing clinical study teams.
• Experience with vendor management and budgeting in clinical trials.

Responsibilities

• Develops Site Activation Plan and starts-up documents as needed.
• Coordinates site identification, selection and recruitment.
• Oversees regulatory and ethics submission processes.
• Manages study milestones, budgets and time entry.
• Oversees vendor contracts and investigator payments.
• Monitors data quality and ensures TMF and source data verification.

Skills

Communication skills

Project management

Team leadership

GCP/ICH knowledge

Stakeholder management

Education

Life Science degree

Nursing background

Job description

Linical is seeking a Clinical Trial Manager to oversee studies, develop project documents, manage budgets, and ensure metrics and timelines are met. You will lead and train CRAs, coordinate with PM, clients and study teams, and supervise third-party vendors.

Key responsibilities include site activation planning, regulatory submissions oversight, monitoring plan development, budget negotiation, and performance reviews. Requires 3+ years in clinical trial management and life science background.