MENU
   
Bienvenido!! "Registro" "o" "Login"
January 19 2019  SpanishSpanish

    Detalles de Empleo

Oferta de trabajo: Study Start up Manager (SCRA level):

La descripción del trabajo.:

Empleo:
Apply for job Save job
   » Company:
Covance
   » Location:
Munich, Germany
   » Salary:
negotiable / month
   » Job type:
Full-Time
   » Posted:
6 hours ago
   » Category:
Customer Service

At Covance, you’ll redefine what’s possible and discover your extraordinary potential. You’ll have the opportunity to personally advance scientific research and make a difference in peoples’ lives with your bold ideas and unique point of view. We are looking for a Clinical Operations Manager (Study Start Up) to be office based in Munich and working for one of our clients.Responsibilities:Accountable for execution and oversight of local operational clinical trial activities for assigned protocols in compliance with ICH/GCP and country regulations, client policies and procedures, quality standards and adverse event reporting requirements internally and externallyOwnership of country and site budgets; development, negotiation and completion of Clinical Trial Research Agreements; oversight and tracking of clinical research-related payments; payment reconciliation at study close-out; oversight and maintenance of financial systemsResponsible for execution and oversight of clinical trial country submissions and approvals for assigned protocols; development of local language materials including local language Informed Consents and translations; interactions with IRB/IEC and Regulatory Authority for assigned protocolsResponsible for managing country deliverables, timelines and results for assigned protocols to meet country commitments; responsible for quality and compliance in assigned protocols in country; contribution to the development of local SOPs; overseeing Clinical Trial Coordinators as applicableCoordinates and liaises with Country Research Manager, Clinical Trial Coordinator, Clinical Research Associate, (Finance and Legal if appropriate) to ensure country deliverables are obtained for submissions, budgets, Clinical Trial Research Agreements and local milestones; collaborates closely with Regional Operations to align country timelines for assigned protocolsOversight and coordination of local processes; clinical and ancillary supplies management, im- and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management; enters and updates country information in clinical systemsRequirements:Degree in Sciences or equivalent experience in a similar roleProven experience in a similar role within a CRO or Pharmaceutical company English fluent written and oralAbility to instruct and lead teams degree in life sciences OR equivalent experience in similar positionAccountable for execution and oversight of local operational clinical trial activities for assigned protocols in compliance with ICH/GCP and country regulations, client policies and procedures, quality standards and adverse event reporting requirements internally and externallyOwnership of country and site budgets; development, negotiation and completion of Clinical Trial Research Agreements; oversight and tracking of clinical research-related payments; payment reconciliation at study close-out; oversight and maintenance of financial systemsResponsible for execution and oversight of clinical trial country submissions and approvals for assigned protocols; development of local language materials including local language Informed Consents and translations; interactions with IRB/IEC and Regulatory Authority for assigned protocolsResponsible for managing country deliverables, timelines and results for assigned protocols to meet country commitments; responsible for quality and compliance in assigned protocols in country; contribution to the development of local SOPs; overseeing Clinical Trial Coordinators as applicableCoordinates and liaises with Country Research Manager, Clinical Trial Coordinator, Clinical Research Associate, (Finance and Legal if appropriate) to ensure country deliverables are obtained for submissions, budgets, Clinical Trial Research Agreements and local milestones; collaborates closely with Regional Operations to align country timelines for assigned protocolsOversight and coordination of local processes; clinical and ancillary supplies management, im- and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management; enters and updates country information in clinical systems
Apply for job Save job

Share:

E-Mail:

Search European Jobs
Related job

Beauty Expert (w/m) Voll-/ Teilzeit

searcheuropeanjobs
Munich, Germany

Featured Full-Time

search european jobs is the leading professional social networking website for professionals to expand their network in the search for new employment and for employers to find new recruits. Learn more
   »
   »
   »
   »

Learn About us

   » About us
   » Contact Us
   » Privacy and Terms

Our other Job Sites

   » Search American Jobs
   » Expertini Job Search
   » Search Canada Jobs
   » Search UK Jobs
   » Search Australian Jobs
   » Search NZ Jobs

Download our Mobile Apps

© 2018 Developed by iExpertini - Web and App Developers
Cookies, Privacy and Terms

Competencia/cualificación:

Categorí­a del Empleo: Otras [ Ver todos Otras  ]
Requerimientos de Idioma:
Tipo de Empleo:
Sueldo: No especificado
Titulación: Sin especificar
Experiencia: No especificado
Localización del Empleo: Munich, Germany, otro
Tipo de empresa Empleador
Día de envío: 2019/01/12 / Viewed 4 times
Información de Contacto
Empresa:


Aplicación Online


BÚSQUEDA DE EMPLEO


Categoría de Empleo:
Localización del Empleo:   
Escriba las palabras clave (Ej: comercial, linux...):