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Clinical & Medical affairs Sr Manager

Ubicación: 

Sant Cugat del Valles, ES

Tipo de Contrato:  Indefinido tiempo completo
Área:  Ensayos Clínicos
Número de solicitud de puesto:  87219

For more than 75 years, Grifols has worked to improve the health and well-being of people around the world. We are a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care.

Headquartered in Barcelona, Spain, Grifols has over 20.000 employees in 30 countries. Grifols’ three main divisions - Bioscience, Diagnostic and Hospital - develop, manufacture and market innovative products and services available in more than 100 countries.

With the world's largest network of plasma donation centers, Grifols, through its Bioscience Division, is a leading producer of essential plasma-derived medicines for the treatment of rare, chronic, and sometimes life-threatening conditions. To help ensure a reliable and consistent source of plasmaderived medicines worldwide, we have an integrated production process that begins with plasma collection and continues through fractionation and purification at our three facilities located in Spain (Barcelona) and the United States (Clayton, North Carolina, and Los Angeles, California). Key products include immunoglobulins, alpha-1 antitrypsin, albumin, clotting factors and specialty products.

Join Grifols!

 

In our Bioscience Division, working at Instituto Grifols company, we are looking for a Clinical and Medical Affairs Senior Manager for Quality and R&D Department.

 

What are your Responsabilities

 

  • You will coordinate the MD group to provide strategic direction, review and approval for the design of clinical programs. 
  • You will provide strategic direction, planning, team management and review for the medical aspects at the global level of all clinical programs of bioscience products.

  • You will assess and eventually follow joint projects with external companies/institutions.

  • You will review strategically and approve the interpretation of any clinical trial/clinical study. 

  • You will provide consultation to Drug Safety and Regulatory Affairs to ensure medical safety assurance.

  • You will provide Regulatory Affairs with the feedback, review and approval of the medical information required to be submitted to, or requested by, Health Authorities, for all clinical programs.

  • You will interface with Health Authorities, external investigators, clinical experts, medical organizations and internal teams/departments. 

 

Who you Are

 

  • You have a Medicine Degree with a Speciality and a minimum of 6 year experience in a CRO, pharmaceutical company or hospital in clinical/medical/pharmacovigilance department.
  • You enjoy working within a multicultural environment, and you have previous experience in a global role with a strong international exposure.
  • You have availability to travel occasionally at an international level.
  • You have an Advanced level of English.

 

 

What we Offer

 

  • Contract of Employment: Permanent Position.
  • Location: Sant Cugat del Vallès.

 

It is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment.

 

We look forward to receiving your application!

 

 

Location: SPAIN : España : Sant Cugat del Valles:SC3 

 

Learn more about Grifols