Manager, Clinical Monitoring

Buscojobs; Lazio; Remoto; EUR 60.000 - 100.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking a dedicated Manager for Clinical Monitoring to lead a team of Clinical Research Associates. This exciting opportunity involves overseeing CRA services, ensuring quality standards, and providing career development support. The role emphasizes strong leadership and management skills, with a focus on fostering a collaborative environment. As a key player in clinical research operations, you will be instrumental in driving departmental goals and enhancing productivity. If you are passionate about clinical research and have a proven track record in managing teams, this role is perfect for you.

Competenze

• 7+ years in clinical operations with 5+ years in oncology trials.
• 3-5 years of supervisory experience managing CRAs.

Mansioni

• Manage and develop CRA workforce to improve quality and productivity.
• Conduct site visits and mentor CRA staff for career growth.

Conoscenze

Clinical Operations

People Management

Oncology Trials Experience

ICH-GCP Mastery

Proficiency with EMRs and EDCs

Problem-Solving Skills

Effective Communication

Formazione

Degree in Scientific or Healthcare Discipline

Descrizione del lavoro

Precision for Medicine is growing! We are hiring a Manager, Clinical Monitoring based in Italy. The position can be fully remote.

Position Summary

The Manager, Clinical Monitoring (GCM) offers a development path for clinical research professionals. Responsibilities include managing and developing the organization's Clinical Research Associate (CRA) workforce and supporting departmental initiatives to improve quality and productivity.

This role requires leading, managing, and motivating a team of CRAs to uphold Precision for Medicine's standards of quality. The manager will ensure proper resource allocation, provide career development support, and minimize turnover.

Essential Functions

1. Develop action plans and oversee CRA services to meet quality and departmental goals.
2. Assist with project resourcing, update tracking systems, and coordinate with project teams.
3. Collaborate with clinical leads and management to meet resource and site requirements.
4. Mentor and manage CRA staff, fostering their skills and career growth.
5. Conduct site visits to assess CRA skills and address project issues.
6. Identify quality risks, recommend corrective actions, and report to leadership.
7. Ensure staff have necessary resources, training, and system access.
8. Maintain metrics for CRA oversight and participate in hiring and onboarding processes.
9. Represent Precision for Medicine professionally.
10. Manage CRA staff in accordance with company policies.
11. Perform additional duties as assigned by leadership.

Qualifications

• Degree in a scientific or healthcare discipline or equivalent experience.
• Minimum 7 years in clinical operations or related fields, with at least 5 years on-site monitoring experience, especially in oncology trials.
• 3-5 years of supervisory experience managing CRAs.
• Ability to travel domestically and internationally (~25%).

Skills and Competencies

• Mastery of ICH-GCP, local regulations, SOPs, and all phases of clinical studies.
• Strong emotional intelligence and people management skills.
• Ability to develop training plans and hold personnel accountable.
• Deep understanding of clinical research operations and site management.
• Proficiency with EMRs and EDCs.
• Highly organized, proactive problem-solver, and effective communicator.
• Professionalism and ability to deliver presentations.

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