Project Manager

 

Recruiter:

Luelle Consulting

Job Ref:

JHB001962/CZ

Date posted:

Monday, October 31, 2022

Location:

Pretoria, South Africa

Salary:

500 000


JOB SUMMARY:
Project Manager – PTA
R500k – R600k
 
Join a global leader in the pharmaceutical industry, my client is looking for a professional with exceptional project management skills. The successful candidate will be responsible for the overall planning, designing and implementation of assigned client projects.

JOB DESCRIPTION:

The successful incumbent will be responsible for:
  • Assisting with creation, as applicable, and maintains a project timeline based on client needs.
  • Assisting with the setup and implementation of clinical studies including, but not limited to, distribution of clinical trial material and ancillary supplies to ensure accurate and timely receipt to client of study materials. In some cases this role may be required to manage the setup and implementation.
  • Reviewing all client specific project details including the packaging, labeling, and distribution of clinical trial material and ancillary supplies with maximum attention to accuracy.
  • Reviewing and approving packaging, distribution, and return documents, as applicable
  • Reviewing and monitoring inventory thresholds and expiry dating, update client as needed data
  • Assisting in sourcing material as outlined in client specific documentation throughout the history of the project.
  • Providing distribution solutions for cold chain supplies and controlled temperature shipment needs
  • Partnering with other team members in Operations to ensure processes and procedures are maintained.
  • Working with team members to address, research and resolve issues and concerns raised by clients
  • Ensuring project activities are documented and billed correctly.
  • Partnering with Quality Assurance to develop or revise applicable documents (i.e., SOPs, Work Instructions, etc.).
  • Partnering with Quality Assurance and team members to ensure compliance of SOPs and correct deviations in a timely manner.
The ideal candidate has:

  • 0-3 years of related work experience working with the principles and practices involved in cGMP and Clinical Trial Management
  • Bachelor’s degree or equivalent knowledge
  • Fluent in German and / or English. Any additional language is an asset.

NB!!! This role can be remote (but a training period of 4 to 6 weeks is required on site in Germany at the beginning + another couple of weeks after +/- 3 months in the role).

Position needs to be filled URGENTYLY!!! Apply now.


Please note the above is the minimum criteria to be considered for the position – If you do not meet the criteria, you will not be shortlisted.

NB - If you have not heard back from us in 2 weeks, please consider your application unsuccessful. Your CV will however be kept on our database for any future positions that may match your skills and competencies

 

NB! This job is now closed. You can apply for other jobs by uploading your CV.



 

 

 

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