Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Trial Supply Manager - Clinical Research
Eingestellt von Elevate Direct
Gesuchte Skills: Sap, Design
Projektbeschreibung
TRIAL SUPPLY MANAGER/BEERSE, BELGIUM/10 MONTHS CONTRACT/UP TO 57 EUR PER HR
This individual contributor is responsible for the management of clinical supplies during the execution phase of clinical trials consistent with GMP guidelines.
DESCRIPTION OF THE ROLE;
Adopt supply strategies in view of changes in trial execution and ensure a seamless transition from study design phase.
Assess clinical study recruitment rates and ensure supply planning is adopted accordingly.
Utilize business tools to manage inventories at depots and sites and ensure on-time delivery with minimal overage of clinical supplies.
Conduct issue resolution activities for supply aspects of clinical studies (eg, packaging, distribution).
Establish and modify trial specific distribution agreements
Member of appropriate GCO clinical trial team.
Develop strong internal collaboration with GCO stakeholders to ensure customer satisfaction.
Interface with Global Trial Managers.
Manage trial supply budget.
Develop excellent working relationships with the other groups within Supply Management.
FOCUS AND SCOPE:
Responsible for the management of all clinical supplies during trial execution
NON TECHNICAL SKILLS AND ADDITIONAL DETAILS:
CRITICAL EXPERIENCES REQUIRED:
A university/bachelor's degree (or equivalent experience) and 4-6 years experience preferably in a clinical supply related role
Experience with clinical supply demand management tools preferred (eg, tcVisualize, IVRS, SAP) Experience with the following functions preferred: clinical supply pack/label/distribution, clinical trial operations, project management, pharma/bio research and development, inventory management
General knowledge of GxP principles Intermediate to advanced software skills (eg, Microsoft Excel, Powerpoint)
CRITICAL COMPETENCIES:
Excellent written and verbal communication skills
Strong planning and cross-functional coordination skills
Strong attention to detail
Ability to work independently with some coaching
Ability to multi-task and manage complexity
Ability to work in a high pressure environment
Solution oriented
Exceptional collaboration skills
Integrity and Credo Based-actions
THE COMPANY
Johnson & Johnson is an American multinational medical devices, pharmaceutical and consumer packaged goods manufacturer founded in 1886.
This job with Johnson & Johnson is a temporary assignment and is being managed by Kelly Services on behalf of Johnson & Johnson. Successful candidates will be placed at the Johnson & Johnson assignment and managed by Kelly Services
If you match these requirements, please apply in the normal way. Elevate will send you an email, please open, click and action that email and your application will be visible to the hiring organisation directly.
This individual contributor is responsible for the management of clinical supplies during the execution phase of clinical trials consistent with GMP guidelines.
DESCRIPTION OF THE ROLE;
Adopt supply strategies in view of changes in trial execution and ensure a seamless transition from study design phase.
Assess clinical study recruitment rates and ensure supply planning is adopted accordingly.
Utilize business tools to manage inventories at depots and sites and ensure on-time delivery with minimal overage of clinical supplies.
Conduct issue resolution activities for supply aspects of clinical studies (eg, packaging, distribution).
Establish and modify trial specific distribution agreements
Member of appropriate GCO clinical trial team.
Develop strong internal collaboration with GCO stakeholders to ensure customer satisfaction.
Interface with Global Trial Managers.
Manage trial supply budget.
Develop excellent working relationships with the other groups within Supply Management.
FOCUS AND SCOPE:
Responsible for the management of all clinical supplies during trial execution
NON TECHNICAL SKILLS AND ADDITIONAL DETAILS:
CRITICAL EXPERIENCES REQUIRED:
A university/bachelor's degree (or equivalent experience) and 4-6 years experience preferably in a clinical supply related role
Experience with clinical supply demand management tools preferred (eg, tcVisualize, IVRS, SAP) Experience with the following functions preferred: clinical supply pack/label/distribution, clinical trial operations, project management, pharma/bio research and development, inventory management
General knowledge of GxP principles Intermediate to advanced software skills (eg, Microsoft Excel, Powerpoint)
CRITICAL COMPETENCIES:
Excellent written and verbal communication skills
Strong planning and cross-functional coordination skills
Strong attention to detail
Ability to work independently with some coaching
Ability to multi-task and manage complexity
Ability to work in a high pressure environment
Solution oriented
Exceptional collaboration skills
Integrity and Credo Based-actions
THE COMPANY
Johnson & Johnson is an American multinational medical devices, pharmaceutical and consumer packaged goods manufacturer founded in 1886.
This job with Johnson & Johnson is a temporary assignment and is being managed by Kelly Services on behalf of Johnson & Johnson. Successful candidates will be placed at the Johnson & Johnson assignment and managed by Kelly Services
If you match these requirements, please apply in the normal way. Elevate will send you an email, please open, click and action that email and your application will be visible to the hiring organisation directly.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
SAP Entwicklung, Medien/Design