We are looking for a Clinical Supply Chain management, supported by strong technical proficiency in SAP, CLARA, Veeva, MS Office, and Google Suite. Fluent in English, excelling at active listening and clear communication to drive seamless teamwork within agile, highly collaborative environments.
We are looking for you!
...
global clinical distribution lead (sap, clara, veeva, ms office).
- basel, basel-stadt
- posted 1 day ago
- closes 30 november 2026
job details
summary
- basel, basel-stadt
- temporary
- job categoryinformation technology
job details
General Information:
- Start Date: asap
- Latest Possible Start Date: Oct 30, 2026
- Planned Duration of Employment: 1 year
- Extension (for temporary contracts): Likely
- Workload: 100%
- Home Office: Hybrid role - mandatory 3 days a week in our KAU office
- Working Hours: Standard
Tasks & Responsibilities:
As a Global Clinical Distribution Lead, you will play a variety of roles according to your experience, knowledge, and general business/team requirements, such as:
- Manage the On-time Delivery Performance for network supply shipments in the distribution network to meet study requirements and patient demand
- Effective participation and engagement on Protocol Execution Teams (PETs), Global Supply Execution Teams (gSETs), and ad-hoc distribution-related meetings on behalf of PTDS
- Drive resolution of operational and system matters impacting on-time delivery collaborating with providers internal and external
- Execute and coordinate network depot supply in coordination with the Clinical Demand and Supply Leader and other partners as needed
- Lead and participate in cross-functional and internal distribution-related projects and process improvement initiatives supporting the global distribution and PTDS strategy
- Execute with the highest level of accuracy in the CLARA system and perform 1st and 2nd-level diagnostics
- Operate within a GMP-compliant environment, ensuring adherence to quality procedures in place
- Processing event records such as quality incidents as well as CAPAs and Changes (Planned Events) if applicable
Must Haves:
- Degree (BA, BS, MS, MBA) in Business (Operations Management or Supply Chain Management), Biotechnology or relevant field
- 3-4 years’ experience in Clinical Trial Management, logistics, warehouse management, or other Supply Chain disciplines, preferably in the Biotechnology / Pharmaceutical industry
- Strong SAP / ERP systems knowledge and experience
- Experience in cross-functional/cross-cultural and agile organizational models
- You are action-oriented and can influence both internal and external stakeholders
- You demonstrate curiosity, active listening, and a willingness to experiment and test new ideas when appropriate, focusing on continuous learning and improvement
- You have a collaborative and agile mindset, actively looking to contribute to cross-functional teams and develop a self-directed team organization
- You solve problems and can manage complex situations autonomously
- You can manage multiple tasks and priorities
We thank you for your application!
We are looking for a Clinical Supply Chain management, supported by strong technical proficiency in SAP, CLARA, Veeva, MS Office, and Google Suite. Fluent in English, excelling at active listening and clear communication to drive seamless teamwork within agile, highly collaborative environments.
We are looking for you!
General Information:
- Start Date: asap
- Latest Possible Start Date: Oct 30, 2026
- Planned Duration of Employment: 1 year
- Extension (for temporary contracts): Likely
- Workload: 100%
- Home Office: Hybrid role - mandatory 3 days a week in our KAU office
- Working Hours: Standard
Tasks & Responsibilities: ...
As a Global Clinical Distribution Lead, you will play a variety of roles according to your experience, knowledge, and general business/team requirements, such as:
show more- Manage the On-time Delivery Performance for network supply shipments in the distribution network to meet study requirements and patient demand
- Effective participation and engagement on Protocol Execution Teams (PETs), Global Supply Execution Teams (gSETs), and ad-hoc distribution-related meetings on behalf of PTDS
- Drive resolution of operational and system matters impacting on-time delivery collaborating with providers internal and external
- Execute and coordinate network depot supply in coordination with the Clinical Demand and Supply Leader and other partners as needed
- Lead and participate in cross-functional and internal distribution-related projects and process improvement initiatives supporting the global distribution and PTDS strategy
- Execute with the highest level of accuracy in the CLARA system and perform 1st and 2nd-level diagnostics
- Operate within a GMP-compliant environment, ensuring adherence to quality procedures in place
- Processing event records such as quality incidents as well as CAPAs and Changes (Planned Events) if applicable
Must Haves:
- Degree (BA, BS, MS, MBA) in Business (Operations Management or Supply Chain Management), Biotechnology or relevant field
- 3-4 years’ experience in Clinical Trial Management, logistics, warehouse management, or other Supply Chain disciplines, preferably in the Biotechnology / Pharmaceutical industry
- Strong SAP / ERP systems knowledge and experience
- Experience in cross-functional/cross-cultural and agile organizational models
- You are action-oriented and can influence both internal and external stakeholders
- You demonstrate curiosity, active listening, and a willingness to experiment and test new ideas when appropriate, focusing on continuous learning and improvement
- You have a collaborative and agile mindset, actively looking to contribute to cross-functional teams and develop a self-directed team organization
- You solve problems and can manage complex situations autonomously
- You can manage multiple tasks and priorities
We thank you for your application!
share this job.
the application process.
See what comes ahead in the application process. Find out how we help you land that job.
1 of 8apply with randstad.
Applying with us is easy. We will review your application and see if you are a good fit for the job and the company.
2 of 8we'll give you a call.
Our consultant will call you at a suitable time to discuss your application and further career aspirations.
3 of 8getting you registered.
If you’ve never worked with us before, we’ll need some basic additional pieces of information to confirm your eligibility for work.
4 of 8compliance check.
Next, we just need to verify a few things - we’ll make the relevant compliance checks and keep you posted.
5 of 8reference and background check.
As part of the process in ensuring you’re perfect for the role, we’ll make contact with any relevant references you’ve provided.
6 of 8the perfect job for you.
Our expert team will either arrange an interview for the role you’ve applied for, or if they believe there’s a better opportunity, they’ll suggest alternative options too.
7 of 8the interview.
We’ll ensure that you’re fully prepared ahead of your interview and know exactly what to expect - good luck!
8 of 8start your new job.
Congratulations, you’re ready to begin your new job. The team will ensure that you’re fully prepared for your first day.
let similar jobs come to you
We will keep you updated when we have similar job postings.
Thank you for subscribing to your personalised job alerts.