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Clinical Development Specialist (Electrophysiology)
CROFTON PARK, UNITED KINGDOM
A fantastic opportunity for an electrophysiology expert to join this market leading global medical devices comany as part of their elite team of clinical specialists. Covering a region focussing on key accounts including those in London, the South East & Cambridge you will use your experience...
We've expanded the search to "London" to find more jobs with all your keywords
Clinical Trial Manager - Hybrid
WEST DRAYTON, GB
Clinical Trials Manager Contract: 12-Month Contract Location: Greater London (Hybrid role, 3 days onsite required) Rate: £350-£445PD Inside IR35 (Dependant on experience) About the Company: Join a leading biopharmaceutical company dedicated to delivering life-saving therapies. At our...
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...
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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...
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Sr. Manager, Global Trial Optimization
LONDON, GB
The Senior Manager, Global Trial Optimization (GTO) will lead program or study level activities to inform the clinical development strategy, clinical study concepts, study protocols and operational plans that will enable predictable delivery of clinical programs and studies. They will play a key...
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...
Sr Manager Regulatory Affairs
UXBRIDGE, GB
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...
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...
Senior Manager Regulatory Affairs
UXBRIDGE, GB
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 illnesses by...
Medical Writer - Turkish
LONDON, GB
...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...
Medical Writer
LONDON, GB
...account lead(s)/line manager at the earliest stage any potential barriers to successful project completion and suggests solutions Play a pivotal role within the editorial team, always leading by example and demonstrating knowledge of good practice/industry guidelines Recognise where s/he can...
Vice President, Global Clinical Trial Management
LONDON, ENGLAND, UK
Vice President, Global Clinical Trial Management Are you a natural leader and able to inspire others? Do you have the drive, enthusiasm and talent to lead others? Does your ambition match that of our client? Our client is a successful global CRO, a company that has enjoyed a sustained period of...
Clinical Project Coordinator - Entry Level
LONDON, ENGLAND, UK
Job Summary Position: Project Coordinator Location: Office-based, London Overview: This position will provide extensive training and is suitable for recent graduates; internship, industrial placement, NHS or Clinical Trials experience is also beneficial Due to continuous business growth and a...
Manager CTSM Excellence Vendor Management
LONDON, ENGLAND, UK
...of outsourced Clinical Trial Supply Management activities Responsibility to identify the need, the requirements and timelines on external vendors for BNT-wide global clinical trial supply associated activities such as labelling, packaging, storage, comparator and disposable sourcing and...
Regulatory Affairs Manager
50000 - 65000
LONDON, ENGLAND, UK
Job Title: Regulatory Affairs Manager (CTA/ CTR) Job Type: Permanent, full-time Locations: UK, Italy, Spain, Sweden or the Republic of Ireland Remote based Remuneration: 50,000 to 65,000 + benefits Regulatory Affairs Manager opportunity working for a cutting edge Oncology focused global...
English Language Manager
LONDON, ENGLAND, UK
...of outsourced Clinical Trial Supply Management activities Responsibility to identify the need, the requirements and timelines on external vendors for BNT-wide global clinical trial supply associated activities such as labelling, packaging, storage, comparator and disposable sourcing and...
Manager - Management Accounts
LONDON, ENGLAND, UK
...of outsourced Clinical Trial Supply Management activities Responsibility to identify the need, the requirements and timelines on external vendors for BNT-wide global clinical trial supply associated activities such as labelling, packaging, storage, comparator and disposable sourcing and...
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