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Clinical Trial Coordinator (Central London - Hybrid) - UK - FSP - REGISTER YOUR INTEREST
33569
UXBRIDGE, LONDON , UXBRIDGE, LONDON
We are inviting applications to join our UK Clinical Trial Coordinator talent pipeline and a chance to play a pivotal role in some of the most significant clinical studies taking place today Please provide some basic information and upload your CV . Hybrid working, with a central-London based...
Sr Manager Regulatory Affairs
UXBRIDGE, ENGLAND, UNITED KINGDOM
Position: Sr Manager Regulatory Affairs Work Structure: Monday - Friday, 39 hours per week Pay Rate: £58 - £64/hour (Inside IR35) Job Description: We are seeking a seasoned Sr. Manager of Regulatory Affairs to support one or more products from a regional regulatory perspective. As an...
Sr Manager Regulatory Affairs
UXBRIDGE
p strong Position: /strong strong Sr Manager Regulatory Affairs br br Please ensure you read the below overview and requirements for this employment opportunity completely. br /strong strong Work Structure: /strong Monday - Friday, 39 hours per week br strong Pay Rate: /strong £58...
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Sr Manager Regulatory Affairs
UXBRIDGE, UNITED KINGDOM
Position: Please ensure you read the below overview and requirements for this employment opportunity completely. Sr Manager Regulatory Affairs Work Structure: Monday - Friday, 39 hours per week Pay Rate: £58 - £64/hour (Inside IR35) Job Description: We are seeking a seasoned Sr. Manager...
Senior Manager Regulatory Affairs
UXBRIDGE, UNITED KINGDOM
CK Group are recruiting for a Senior Manager Regulatory Affairs to join a biopharmaceutical company who are based in Uxbridge or Cambridge on a contract basis for 12 months. Company: Our client is committed to unlocking the potential of biology for patients suffering from serious...
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Director, Program Operations Leader, Early Clinical Trial Development
45725
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...complex programs in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality, timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and...
Assoc Mgr Clinical Study
60833
UXBRIDGE, LONDON , UXBRIDGE, LONDON
This role is a hybrid position which means the individual must work on-site 3 days per week. Fully remote work is not possible for this role. The position can be based in Armonk, NY or Basking Ridge, NJ. A Clinical Study Associate Manager (CSAM) role supports the Clinical Study Lead (CSL) by taking...
Senior Director, Global Patient Safety - Gene Therapy
62571
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...provide PV input for clinical documents (Investigator Brochures, protocols, clinical study reports, and other relevant study documents) Lead cross-functional meetings including Safety Monitoring Team (SMT) activities Represent GPS for assigned compounds on cross-functional teams, including...
Director, Global Patient Safety Sciences - Hematology
80469
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.) Leads cross-functional Safety Monitoring Team (SMT) activities Represent Global Patient Safety for assigned compounds on cross-functional teams, including Regeneron s Safety Oversight...
Senior Director, Global Patient Safety - Ophthalmology
61932
UXBRIDGE, LONDON , UXBRIDGE, LONDON
...etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.) Leads cross-functional Safety Monitoring Team (SMT) activities Represent GPS for assigned compounds on cross-functional teams, including Regeneron s Safety Oversight Committee (RSOC...
Qualified Person for Pharmacovigilance (QPPV - UK)
HARROW, GB
...strong leadership and managerial capability. Strong English skills (written and spoken). Project management skills and ability to maintain timelines. People management skills and ability to interact with staff at various levels and in various functional areas. Highly process driven with...
Deputy Headteacher
42402
HAYES, MIDDLESEX, UB3
How would you like to be paid for five days but only work four? OFG are taking part in the 4-day working week trial Job Title: Deputy Headteacher Location: Hillingdon Manor School, Uxbridge, Greater London UB8 3HD Salary: Up to £60,000 per annum Hours: 38.5 hours per week Monday to Friday...
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Contract Senior Manager, Global Trial Optimisation
LONDON, ENGLAND, UNITED KINGDOM
Proclinical is seeking a dedicated Manager of Global Trial Optimisation. This role involves overseeing the clinical development strategy, clinical study concepts and protocols as well as operational plans. The successful candidate will play a crucial part in maintaining relationships with external...
Senior Project Clinical Data Manager
GREATER LONDON, GB
Senior Project Clinical Data Manager We have the pleasure of working with a fantastic early phase CRO based in London. The company have a strong leadership team who are accelerating growth and have a great vision for the future. The offices are very modern and they have a fully kitted out clinical...
Clinical Data Manager
LONDON, GB
We are seeking an experienced Data Manager with a proven track record in the life sciences industry (CRO, pharmaceuticals, biotechnology, etc). The ideal candidate will possess a deep understanding of Good Clinical Practice (GCP) and its application in research studies. In addition, they will have...
Clinical Supply Chain Manager
LONDON AREA, UNITED KINGDOM, UNITED KINGDOM
Location: Central London office. Hybrid schedule: 4 days in-office, 1 day remote. As the Clinical Supply Chain Manager, under the Director's guidance, you'll spearhead the setup and oversight of clinical supply chains for studies/programs spanning multiple phases. We're looking for proactive...
Clinical Supply Chain Snr/Manager
LONDON, GB
Location: Central London office. Hybrid schedule: 4 days in-office, 1 day remote. As the Clinical Supply Chain Snr/Manager, under the Director's guidance, you'll spearhead the setup and oversight of clinical supply chains for studies/programs spanning multiple phases. We're looking for proactive...
Clinical Operations Lead
LONDON, GB
We are seeking a highly motivated and experienced Clinical Project Lead to join our dynamic team. The Clinical Project Lead will play a pivotal role in the planning, execution, and management of clinical research projects focused on women's health. This individual will collaborate with...
Medical Writer - Turkish
LONDON, ENGLAND, UNITED KINGDOM
...complex scientific and clinical information into clear and concise documents. Their primary responsibility is to communicate medical and scientific information to various audiences, including healthcare professionals, regulatory agencies, and the public. Responsibilities: Clinical and Regulatory...
Director, Global Development Quality Assurance (GDQA) - Remote
CITY OF LONDON, GB
...Data management, Clinical Trial Supply and Logistics, IRT, Pre-clinical, CMC, Clinical Pharmacology, Translational Sciences, Medical Affairs, Commercial, Regulatory Affairs and Companion Diagnostics. Drive change initiatives in area of expertise in partnership with functional groups...
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