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Plats: Prag, Hlavní město Praha, Tjeckien
Jobb-id R-058556
Datum inlagd: 08/14/2019

·Leadership of dedicated group, building the team spirit, developing team style and behaviour.

·Ensures adequate resources for the studies assigned to the country.

·Ensures that the workload of the team(s) is adequate.

·Development and performance management of the team(s).

·Ensures that everyone in the team has development and training plans, according to IDP process.

·Coaches the team members and all direct reports on a regular basis, and plans/organises coaching with external providers if needed.

·Prepares salary and bonus proposals for all team members based on their performance in close collaboration with responsible CH/CD SMM and local HRBP.

·Contributes to efficient SMM organisation and its functioning at country level by working closely with responsible CH/CD SMM.

·Contributes to high quality feasibility work.

·Oversees successful delivery of SMM study delivery country level targets to plan, with speed and quality.

·Delivers Country budget to plan with agreed RBU targets

·Contributes to the quality improvement of the study processes and other procedures.

·Ensures all systems are continuously updated.

·Ensures completeness and timeliness of the eTMF to maintain it “Inspection Ready”.

·Assists Local Study Managers/teams in forecasting study timelines, resources, recruitment, study materials and drugs.

·Provides direction to LSM/teams on major study commitments including resolving any key issues identified.

·Supports SMM region in initiatives/activities as agreed with Senior Director SMM (Region).

·Ensures collaboration with local Medical Affairs team.

Ensures that study activities at country level comply with local policies and code of ethics.

Clinical Research Manager/Country Head
Development

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