Clinical Trials Supply Chain Specialist

**Our client, a global pharmaceutical company, is currently looking for a Clinical Trials Supply Chain Specialist to join their team in Uxbridge on a full time, 12-month temporary basis (35 hours per week).** You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a...

The Associate Director of Comparator Strategy and Operations is responsible for managing clinical comparator & ancillary supply and sourcing strategies at the asset, program, and study levels for Regeneron clinical trials. The associate director will be part of a team that drive best practices, standardization and optimization of comparator and ancillary...

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...

Manage regional Phase Ib-III clinical studies in the EMEA region. * Draft and coordinate review of study documents like protocols, case report forms, and clinical study reports. * Manage CROs/vendors, coordinate data listings review, and train study personnel. * Work with Clinical Program Managers to manage regional Virology clinical trials. *...

Manage regional Phase Ib-III clinical studies in the EMEA region. * Draft and coordinate review of study documents like protocols, case report forms, and clinical study reports. * Manage CROs/vendors, coordinate data listings review, and train study personnel. * Work with Clinical Program Managers to manage regional Virology clinical trials. * Require...

3 weeks ago Be among the first 25 applicants The CTM role will involve regional management on Phase Ib-III clinical studies, with a strong emphasis on the EMEA region. The successful candidate will be a member of the Global Study team overseen by a Clinical Program Manager. The candidate will likely work across several studies, including involvement from...

My client is seeking an experienced Supply Chain Planner to join their team initially in a 15 month contract. They offer an excellent salary plus benefits including bonus and hybrid working **Role** Maintain precise knowledge of POs, demand forecasts and inventory levels in order to plan and administer the supply of product to meet agreed customer service...

Manage regional Phase Ib-III clinical studies in the EMEA region. * Draft and coordinate review of study documents like protocols, case report forms, and clinical study reports. * Manage CROs/vendors, coordinate data listings review, and train study personnel. * Work with Clinical Program Managers to manage regional Virology clinical trials. * Require...

**Salary**: Negotiable**Job type**: Interim/Contract **Location**: Uxbridge, England **Function**: Clinical Operations, Project Management **Posted**:16/05/2023 **Ref**: BBBH22304 - Hi I'm Emma , I manage this role Hobson Prior are currently looking for a Clinical Supplies Project Coordinator to join a brilliant pharmaceutical organisation on a...

Manage regional Phase Ib-III clinical studies in the EMEA region. Draft and coordinate review of study documents like protocols, case report forms, and clinical study reports.Manage CROs/vendors, coordinate data listings review, and train study personnel.Work with Clinical Program Managers to manage regional Virology clinical trials.Require significant...

**Supply Chain Assistant (8-month FTC)** We have an exciting opportunity for a Supply Chain Assistant to join us on a maternity cover contract. As Supply Chain Assistant, you will support the Supply Chain & Merchandising team by maintaining the quality of system data with accurate data sets, maintenance and reporting. We are a collective of seven luxury...

We are seeking adventurous souls to join our team as a Clinical Trials Manager! If you're passionate about making a difference in healthcare and thrive in dynamic environments, this is the opportunity for you. Dive into the exhilarating world of Virology and be at the forefront of cutting-edge research. Enjoy a supportive and collaborative work...

Regulatory Affairs Operations Senior Associate | Administrator | EU CTR | Clinical Trials A new role for an innovative multinational biopharmaceutical company focusing on discovering and delivering innovative medicines for patients suffering serious illnesses. They are a well-established biotechnology innovator for over 40 years with a focus inoncology,...

**We are currently looking for an Initiation Clinical Research Associate II to join our UK Clinical Study Start-Up Team in Uxbridge.** The **Initiation Clinical Research Associate **(**iCRA**) specializes in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing...

When our values align, there's no limit to what we can achieve.   Parexel are currently recruiting for an Senior Clinical Research Associate, to cover UK sites. In this role, the Senior Clinical Research Associate is responsible for field monitoring and management of clinical sites. This position focuses on all activities required to evaluate,...

When our values align, there's no limit to what we can achieve.   Additional Job Description Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting,...

Great things are happening in the Europe and Australia (EUAU) region. Each day, our 2,500 plus colleagues bring their passion to our offices, manufacturing sites, R&D center, and commercial/distributor markets across Europe, Australia, and New Zealand. We are energized by over 150 years of bringing people together with the food they love. With beloved...

When our values align, there's no limit to what we can achieve.   Parexel FSP is currently looking for a Clinical Operations Manager (Regulatory) to join our expanding team in the UK. This will be a home-based position. Working at Parexel offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors...

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Company: Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human...