Clinical Supply Chain Manager at PSI CRO

Oxford, England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

04 Jun, 26

Salary

0.0

Posted On

07 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Protocols, Supply Chain Solution, Drug Demand Forecast, Campaign Strategy, CMO Vendor Management, Packaging, Labeling, Procurement, Distribution, QP Release, IRT Vendor Management, System Set-up, UAT, Clinical Supply Plans, Vendor Management Plans, Risk Assessment

Industry

Pharmaceutical Manufacturing

Description

Company Description PSI is an award-winning full-service CRO, bringing together more than 3,000 dynamic and knowledgeable individuals working to help impact the future of medicine in more than 50 countries around the world. We support pharmaceutical, biotechnology, and medical device companies with the services needed to perform clinical trials of new medicines. Our work helps patients in need improve their well-being – a fundamental driver for many of us to show up and do our best each day. Job Description In this role, you will undertake activities to assess, plan and set up trial supply schemes for assigned projects and manage vendors involved in clinical supplies and interactive response technology. This is a temporary position to cover a maternity leave period. You will: Analyse clinical trial protocols and translate requirements to establish an efficient supply chain solution for PSI studies Build and maintain a drug demand forecast in line with planned enrolments Plan the optimal campaign strategy, to ensure clinical supplies are available in accordance with the project requirements Manage the CMO vendor - oversee packaging, labelling, procurement, distribution and QP release activities to ensure supplies are delivered on time Manage the IRT vendor - lead study specific system set-up, UAT, system acceptance and ongoing system updates Develop clinical supply plans and provide input for the development of vendor management plans Participate in the selection of trial supply vendors and IRT vendors for PSI studies Support and train PSI teams in clinical supply management Liaise with PSI project teams, company divisions, clients and vendors Assess risks associated with clinical product management and quality incidences reported by vendors Support business development tasks related to clinical trial supply services Qualifications College or University degree 3-5 years experience in Clinical Supply Chain Management (Essential) Experience working with supply chain technologies (i.e. IRT, CTMS, IWRS integration rules and principles) Training in GMP and GDP Ability to communicate effectively with vendors and internal parties Ability to work both independently and in a team environment PC skills to be able to work with MS Word, Excel and PowerPoint Additional Information If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. You will be a part of a a dedicated Vendor Management team, get all support and ownership of your projects.

Responsibilities

The manager will assess, plan, and set up trial supply schemes for assigned projects, managing vendors involved in clinical supplies and interactive response technology. Key duties include analyzing protocols, building demand forecasts, planning campaign strategies, and overseeing CMO and IRT vendor activities.