Detalle de la oferta

13/03/2023

Study Coordinator - Madrid

Otros Departamentos

Madrid (España)

SC is responsible for all local data generation (LDG) and Investigator Initiated Studies (IIS) projects leading the design, planning, execution, analysis and reporting for LDGs and IIS ensuring compliance with federal guidelines and institutional policy. Engage with investigators in non-promotional.

Responsabilities:

• Collaborate in the implementation of the LDG and IIS included on the Medical Affairs Plans
• Support the identification of potential study investigators for sponsored studies, at the request of the clinical trials organization personnel.
• Elaborate documentation related to LDG or IIS which include but are not limited to protocols, reports, presentations and contracts
• Provide scientific support to investigator that are or may be involved in LDG or IIS projects.
• Ensure the highest quality of LDGs and IIS in alignment with the therapeutic areas’ medical objectives.
• Collaborate with local and HQ stakeholders to ensure alignment of strategies to company objectives and to achieve goals within timeline and budget;
• Organize and facilitate department annual local data generation (LDG)
• Collaborate with the Medical Advisor on the management of the LDG and IIS budget
• Communicate with the different stakeholders to ensure the execution of the LDG and IIS which include but are not limited to CRO, pharmacovigilance, legal, compliance.

Ventajas:

- Herramientas de trabajo incluidas.

Tipo de contrato: Fijo discontinuo (12 meses).

30.000 euros bruto fijo anual