Precision Medicine Group

Valoración de la empresa
Madrid
https://www.precisionmedicinegrp.com
Derecho y Contabilidad
Valoración de la empresa

Salario en Precision Medicine Group

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Precision Medicine Group está buscando empleados para puestos:

director

3 en los últimos 201 días, recientemente 2024-04-08
Requisitos
  • informed knowledge of all aspects of the drug development process inclusive of regulatory milestones
  • specialized Knowledge of the Clinical Trial Information System under the Clinical Trial Regulation
  • experience of regulatory activities including but not limited to submissions to Regulatory Authorities, including INDs/CTAs and amendments, ODDs and PIPs
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Ofertas actuales para el puesto:

Senior Director / Executive Director / VP, Regulatory Affairs Madrid

Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced...

Puesto de trabajo: director
2024-04-06

Senior Director / Executive Director / Vp, Regulatory Affairs (M-603) Madrid

.Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced...

Puesto de trabajo: director
2024-03-27

Associate Director, Regulatory Affairs Madrid

The Associate Director of Regulatory Affairs will lead teams by providing regulatory strategy and support for all International (inc. North America) regulatory submissions. The role will lead and support teams for all regulatory submissions and activities in relation to Clinical Trials and drug development. The position will lead and support teams and efforts around filing activities, Health...

Requisitos: 8+ years or more relevant regulatory affairs experience working for a Clinical Research Organisation, Pharmaceutical or Biotech company, informed knowledge of all aspects of the drug development process inclusive of regulatory milestones, specialized Knowledge of the Clinical Trial Information System under the Clinical Trial Regulation, experience of regulatory activities including but not limited to submissions to Regulatory Authorities, including INDs/CTAs and amendments, ODDs and PIPs
Puesto de trabajo: director
2023-09-20

Associate Director, Site Contract Management (Europe)bal head) Alcobendas

Software: MS Project
Puesto de trabajo: director
2022-06-26

Associate Director, Site Contract Management (Europe)bal head) Madrid

Requisitos: degree or equivalent experience ideally in a Law or healthcare discipline, experience leading teams as LM or by Projects, experience in contract research, life science, biotech or pharmaceutical industry is preferred
Puesto de trabajo: director
2022-06-24

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biostatistician

5 en los últimos 34 días, recientemente 2022-06-27
Ofertas actuales para el puesto:

Tiempo Para Reconstruir Con Manager Biostatistics Principal Biostatistician A Precision Medicine Group Estamos Contratando Alcobendas

Puesto de trabajo: biostatistician
2022-06-25

Manager, Biostatistics / Principal / Lead Biostatistician Alcobendas

Puesto de trabajo: biostatistician
2022-06-27

Manager, Biostatistics / Principal / Lead Biostatistician Madrid

Puesto de trabajo: biostatistician
2022-06-25

Manager, Biostatistics / Principal Biostatistician Alcobendas

Puesto de trabajo: biostatistician
2022-06-03

Manager, Biostatistics / Principal Biostatistician Madrid

Puesto de trabajo: biostatistician
2022-05-25

Salario en otras empresas en el puesto biostatistician

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