Clinical Trial Supply Manager / no-825

Location
CH-Basel
Start
01.07.2022
End
01.06.2023
Workload
80-100% %
All-in / Hour
Please see Job Description
Total Hours
2096

Deadline:

Deadline
27.06.2022

 

Clinical Trial Supply Manager / no-825

Location
CH-Basel
Workload
80-100% %

Start

01.07.2022

End

01.06.2023

DEADLINE

Deadline
27.06.2022

  • CH-Basel
  • CH-Basel01.07.202201.06.202380-100% % 2096Please see Job DescriptionDeadline
    27.06.2022

For our customer located in Basel/Switzerland we are currently looking for a: Clinical Trial Supply Manager (m/f/x)

  • Branch: Pharma
  • Gross Rate (given by client): 55,77 – 62,74 CHF/hr gross

Tasks & Responsibilities

Major accountabilities:

  • Represents GCS as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT on the optimal clinical trial supply strategy in terms of, but not limited to, packaging design, technical and timeline feasibility, efficiency, and risk management.
  • Reviews overall clinical trial protocol/protocol amendments, provides inputs to develop optimal packaging design, clinical trial supply design and visit schedule
  • Creates and maintains complete and accurate clinical supply demand for assigned study in alignment with protocol requirements, key study parameters and milestones, patient projections, with appropriate overage and by using defined processes and systems.
  • Creates and drives finalization of the packaging design (Clinical Packaging Request) and a comprehensive label strategy for all participating countries in the clinical trial.
  • Defines clinical supply parameters for NIRT set up and initiates subsequent updates throughout the duration of the clinical trial
  • Develops and executes a trial-level project plan together with all other relevant roles.
  • Identifies, assesses and proactively communicates supply risks to all relevant stakeholders along with appropriate mitigation strategies to ensure supply continuity
  • Collaborates with all relevant line function partners for country submission and approval timelines (including INDIMPD
    amendment) to develop optimal supply strategy.
  • Generates optimal distribution plans for investigational medicinal products (IMPs), jointly with partner functions. Triggers and tracks shipments of IMPs from central depot to regional hubs and local depots.
  • Develops, maintains and executes an optimal resupply strategy with proactive planning, appropriate lead-time, and replenishment quantities to ensure compliance and continuity of clinical supplies, including proactive expiry management of clinical supplies.
  • Is responsible to consolidate, maintain and track the clinical trial budget with key stakeholders for overall GCS external cost (e.g., labels, packaging, distribution, and comparators).
  • Actively contributes to the GCS sub team as a full member. Ensures adequate, proactive exchange of relevant knowledge & information between the GCS sub team and the CTT.
  • Fully supports, prepares the GCS PL to adequately address GCS considerations at various cross-functional teams e.g., TRD sub team, ICT, etc.

Must Haves

Minimum requirements:

 

  • Bachelor or University degree
  • High learning agility
  • Analytical / critical thinking enjoying working with data and digital and attention to detail
  • Fluent in English
  • Basic project management, good organization, and planning skills
  • Demonstrates problem-solving and idea generation skills
  • Good presentation skills
  • Fundamental Leadership skills.
  • Very good communication, negotiation, and interpersonal skills. Ability to work in interdisciplinary teams

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

  • CH-Basel
  • CH-Basel01.07.202201.06.202380-100% % 2096Please see Job DescriptionDeadline
    27.06.2022

For our customer located in Basel/Switzerland we are currently looking for a: Clinical Trial Supply Manager (m/f/x)

  • Branch: Pharma
  • Gross Rate (given by client): 55,77 – 62,74 CHF/hr gross

Tasks & Responsibilities

Major accountabilities:

  • Represents GCS as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT on the optimal clinical trial supply strategy in terms of, but not limited to, packaging design, technical and timeline feasibility, efficiency, and risk management.
  • Reviews overall clinical trial protocol/protocol amendments, provides inputs to develop optimal packaging design, clinical trial supply design and visit schedule
  • Creates and maintains complete and accurate clinical supply demand for assigned study in alignment with protocol requirements, key study parameters and milestones, patient projections, with appropriate overage and by using defined processes and systems.
  • Creates and drives finalization of the packaging design (Clinical Packaging Request) and a comprehensive label strategy for all participating countries in the clinical trial.
  • Defines clinical supply parameters for NIRT set up and initiates subsequent updates throughout the duration of the clinical trial
  • Develops and executes a trial-level project plan together with all other relevant roles.
  • Identifies, assesses and proactively communicates supply risks to all relevant stakeholders along with appropriate mitigation strategies to ensure supply continuity
  • Collaborates with all relevant line function partners for country submission and approval timelines (including INDIMPD
    amendment) to develop optimal supply strategy.
  • Generates optimal distribution plans for investigational medicinal products (IMPs), jointly with partner functions. Triggers and tracks shipments of IMPs from central depot to regional hubs and local depots.
  • Develops, maintains and executes an optimal resupply strategy with proactive planning, appropriate lead-time, and replenishment quantities to ensure compliance and continuity of clinical supplies, including proactive expiry management of clinical supplies.
  • Is responsible to consolidate, maintain and track the clinical trial budget with key stakeholders for overall GCS external cost (e.g., labels, packaging, distribution, and comparators).
  • Actively contributes to the GCS sub team as a full member. Ensures adequate, proactive exchange of relevant knowledge & information between the GCS sub team and the CTT.
  • Fully supports, prepares the GCS PL to adequately address GCS considerations at various cross-functional teams e.g., TRD sub team, ICT, etc.

Must Haves

Minimum requirements:

 

  • Bachelor or University degree
  • High learning agility
  • Analytical / critical thinking enjoying working with data and digital and attention to detail
  • Fluent in English
  • Basic project management, good organization, and planning skills
  • Demonstrates problem-solving and idea generation skills
  • Good presentation skills
  • Fundamental Leadership skills.
  • Very good communication, negotiation, and interpersonal skills. Ability to work in interdisciplinary teams

Did we catch your interest?

The SimplyVision-Team is looking forward to receive your application (Word file is highly appreciated).

Kindly be informed that our customer is located in Switzerland. Therefore only applications from candidates within the EU or candidates holding Swiss work permission are required.

Files must be less than 5 MB.
Allowed file types: txt rtf pdf doc docx.
If not - no problem - we'll organize one.
More optional Information about your way of finding us
You agree that your data will be used to process your request. Further information and revocation instructions can be found in the privacy policy.


You can apply to this job and others using your online resume. Click the link below to submit your online resume and email your application to this employer.

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