Senior Clinical Trial Submission Administrator

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...

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,...

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...

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...

**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...

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...

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,...

**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...

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...

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...

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 therapeutics....

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...

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...

CK Group are recruiting for a Regulatory Affairs Manager CMC 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...

CK Group are recruiting for a Regulatory Affairs Manager CMC 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 therapeutics....

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. Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This...

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. Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This...

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...