Country Study Operations Manager I - France - FSP

Parexel; Paris; Hybride; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading clinical research organization in France is seeking a Country Study Operational Manager to implement study plans and manage vendor relationships. This role requires a minimum of 5 years in clinical trial management, excellent leadership and organizational skills, and a relevant nursing or advanced degree. Join us to contribute significantly to the success of clinical studies and patient well-being.

Qualifications

• Minimum of 5 years of relevant clinical trial management experience.
• Excellent leadership, communication, and organizational skills.
• Able to multi-task under limited direction.

Responsabilités

• Implement Start-up and Site Activation Plans.
• Develop study level plans for recruitment strategy.
• Manage country/vendor oversight and coordination.

Connaissances

Clinical trial management

Leadership

Communication

Organizational skills

Multi-tasking

Formation

M.S / M.A / Ph.D or B.A / B.S / nursing degree

Description du poste

Some specifics about this advertised role

Regional / Country / Study level implementation of Start-up and Site Activation Plans

Responsible for country / study level Recruitment Strategy

Responsible to support the development of study level plans

Communication with the local team and internal stakeholders and CRO partner as applicable and as listed above to ensure efficient and timely study delivery of the agreed plans

Responsible for study and / or country vendor management and oversight including follow up and coordination of vendor deliverables

The Country Study Operational Manager will be able to work independently and exercise their own judgement.

Who are Parexel

Parexel supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client base.

We supported the trials of most of today’s top 50 best-selling drugs, but equally we enable more niche drug developments that are critical to the well‑being of many patients.

You’ll be an influential member of the wider team.

What we are looking for in this role

For every role, we look for professionals who have the determination and courage always to put patient well‑being first. That to us is working with heart.

Here are a few requirements specific to this advertised role.

Minimum of 5 years of relevant clinical trial management experience.

Excellent leadership, communication, and organizational skills. Able to multi‑task under limited direction and on own initiative.

M.S / M.A / Ph.D or B.A / B.S / nursing degree is essential.

Prior and demonstrable experience working at a senior level within Study start up preferred.