Clinical Project Manager Onco (Temp)en Barcelona.
detalle oferta
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tipo de contrato Temporal
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jornada Completa
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modalidad Combinada (teletrabajo y presencial)
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sector Química Farma
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salario
no informado -
puesto
jefe proyecto -
nº vacantes
1 -
localidad
Barcelona -
provincia
Barcelona -
especialidad
Life Sciences -
subespecialidad
Pharma y Biotech - Medico
¿tienes alguna duda?
Amplía la información sobre el proceso contactando con:
Patricia Felipe
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our client
AstraZeneca is looking for a Clinical Project Manager for its global hub in Barcelona for a temporary contract.
ver menos ver másyour functions
Provides operational expertise to the study team.
Lead the development of study documents as appropriate as well as any updates/amendments, ensuring template and version compliance.
Manage the set-up of third-party vendors, assessing initial statement of work and budget, as well as the change order process.
Ensure the supply of Investigational product and study materials by liaising with Drug Supply or external service providers as appropriate.
Oversight of third party vendors, global / local internal staff and investigator sites to support effective delivery of a study and its regulatory documents from development of the protocol through to the Clinical Study Report.
Provide oversight of and support recruitment and data delivery as well as risk mitigation strategies.
Oversee the clinical trial insurance process; track approvals, revisions and renewals of certificates.
Monitor study conduct and progress, proactively identifying and resolving issues which may impact delivery of the study to the necessary quality, timelines or budget.
Drive risk management and quality efforts to ensure study compliance.
Prepare presentation material for meetings, newsletters and websites.
Direct the study team in the implementation of audits and regulatory inspections.
position requisites
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Formación
: Licenciado: Biología -
Idiomas
: Inglés: C1 -
Conocimientos
: ensayos clinicos -
Experiencia
: 2 años
University degree / Bachelor¿s degree, preferably in medical or biological science, or discipline associated with Clinical Research, or equivalent experience
Deep understanding of the drug development process with minimum of 5 years clinical trial experience, of which at least 2 years are in global study management
Experience of working with and delivering through strategic partners and 3rd party vendors
Excellent knowledge of ICH-GCP principles
Team orientated
Ability to lead, coordinate and prioritise multiple tasks and deliverables
Proactive approach
High degree of flexibility
Demonstrated verbal and written communication skills
Good negotiation and collaboration skills
Demonstrated interpersonal and problem-solving skills
Ability to manage change and actively seek and champion more efficient and effective ways of working
Ability to coach & act as a buddy for more junior colleagues
Some travel may be required
your benefits
- Temporary contract of at less than nine months
- Immediate incorporation
- Attractive compensation package
- Smartworking policy
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publicado el 03/11/2024 · 376 visitas y 18 inscritos
este anuncio se cerrará el 03/05/2025