[JW066] | Manager, Clinical Monitoring (English And French Speaking)

Precision For Medicine; Santiago de Compostela; A distancia; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading clinical research organization is seeking a Manager, Clinical Monitoring to join their European team. This role encompasses managing the CRA workforce, optimizing clinical research operations, and ensuring high-quality delivery of goals. The ideal candidate will have a postgraduate degree, fluency in English and French, and significant experience in clinical operations, particularly in oncology trials. This position can be fully remote from Spain, Hungary, or other listed locations.

Formación

• Fluent in English and French.
• At least 7 years in clinical operations or related fields, with 5+ years onsite monitoring experience, especially in oncology trials.
• 3-5 years of supervisory experience managing CRAs.

Responsabilidades

• Develop action plans and oversee strategies to optimize CRA services.
• Manage and coach CRA staff to uphold quality standards.
• Conduct site visits to assess CRA skills and address developmental needs.

Conocimientos

Leadership

Team management

Problem-solving

Communication

Training development

Educación

Graduate or postgraduate degree in a scientific or healthcare discipline

Herramientas

EMRs

EDCs

Descripción del empleo

Precision for Medicine is growing!
We are hiring a Manager, Clinical Monitoring to join our European team.
This position can be fully remote from the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia.

Position Summary:

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

This role requires the ability to independently lead, manage, and motivate a team of CRAs (employees and/or consultants) to standards aligned with Precision for Medicine's values and focus on quality. The position ensures proper resource allocation to projects, provides career development support to CRAs, and maintains high employee satisfaction.

Key Responsibilities:

1. Develop action plans and oversee strategies to optimize CRA services, ensuring high-quality delivery of goals.
2. Assist with project resourcing, ensuring appropriate allocation of resources per project phase.
3. Update tracking systems and collaborate with project teams.
4. Work with Clinical Team Leads and Clinical Operations Management to meet resource and site requirements.
5. Develop, mentor, manage, and coach CRA staff to uphold quality standards.
6. Support CRA career development and accountability.
7. Conduct site visits to assess CRA skills and address developmental needs.
8. Identify quality risks, recommend corrective actions, and address performance deficiencies.
9. Ensure staff have necessary resources, training, and system access.
10. Oversee timely and accurate administrative updates (SOPs, T&E, etc.).
11. Participate in improving CRA procedures and metrics evaluation.
12. Contribute to the interview process and onboarding of new CRAs.
13. Represent Precision for Medicine professionally and manage staff according to company policies.

Qualifications:

• Graduate or postgraduate degree in a scientific or healthcare discipline.
• Fluent in English and French.
• At least 7 years in clinical operations or related fields, with 5+ years onsite monitoring experience, especially in oncology trials.
• 3-5 years of supervisory experience managing CRAs, including developing training and evaluation processes.
• Willingness to travel domestically and internationally (~25%).

Skills and Competencies:

• Mastery of ICH-GCP, local regulations, SOPs, and all study phases.
• Strong emotional intelligence and people management skills.
• Ability to develop training plans, work independently, and motivate teams.
• Deep understanding of clinical research operations and site management.
• Proficiency with EMRs and EDCs.
• Highly organized with excellent problem-solving skills.
• Professionalism, punctuality, and positive interpersonal interactions.
• Ability to deliver presentations effectively.

Additional Information:

Data collected will be stored according to our Privacy Policy. We are an Equal Opportunity Employer. For accommodations, contact us as specified in the application process.