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Pharmaceutical Project Manager (Clinical Trials/ Clinical Supply Chain)

Gibbs Hybrid
Posted 8 hours ago, valid for 2 hours
Location

Prenton, Merseyside CH43 3ET, England

Contract type

Full Time

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • The contract role is for a Pharmaceutical Project Manager specializing in Clinical Trials and Clinical Supply Chain, located in Liverpool with a hybrid work option.
  • This position is a 12-month contract aimed at supporting the External Manufacturing Quality team due to the insourcing of newly acquired clinical trials.
  • Candidates must have a degree or equivalent experience, along with essential project management experience and preferred previous pharmaceutical quality experience.
  • The role requires strong skills in process improvement, relationship building, and knowledge of clinical trial documentation submission and approval.
  • Compensation details are not specified, but the role emphasizes the importance of experience in project management and the pharmaceutical sector.

Contract Role - Pharmaceutical Project Manager (Clinical Trials/ Clinical Supply Chain) -- Liverpool/Hybrid - 12 Months Initial

We are seeking an experienced Pharmaceutical Project Manager (Clinical Trials/ Clinical Supply Chain) to support the External Manufacturing Quality team, due to the insourcing of newly acquired acquisition clinical trials.

Role Overview:• Job Title: Pharmaceutical Project Manager (Clinical Trials/ Clinical Supply Chain)• Location: Liverpool/Hybrid• Contract Type: Contract • Duration: 12 months initially• Sector: Pharmaceutical

Serves as Project Manager for prioritizing and alignment of external Qualified Person (QP) release of clinical supplies at Contract Manufacturing Organisations (CMOs).Partner with Regulatory Affairs and Global Clinical Supply Chain to ensure on-time delivery of Health Authority approvals for release of clinical supplies (as applicable).

Qualifications & Experience• Degree qualified or equivalent experience required.• Project Management experience is essential.• Previous Pharmaceutical Quality experience is desired/preferred.• Demonstrated experience leading initiatives related to continuous improvement and/or implementation of new ways of working.• Demonstrated ability to build and leverage relationships through diplomacy with a broader focus?within the Function.• Experienced in process improvement.• Ability to recognize the potential impact on internal/external challenges on the future state success.• Good knowledge/experience in computer systems (MS, excel, word, etc.).• Ability to co-ordinate/lead meetings.• Knowledge of clinical trial documentation submission and approval preferred.

Please feel free to contact myself - Daisy Nguyen at Gibbs Consulting for a confidential chat to know more details about the role.

Please also note: Due to the volume of applications received for positions, it will not be possible to respond to all applications and only applicants who are considered suitable for interview will be contacted.

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In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.