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Regulatory Affairs Manager
WINDSOR, ENGLAND, UNITED KINGDOM
...submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team (GRPT) and study teams within the development operations organization. Ensure study deliverables...
Regulatory Affairs Manager
WINDSOR, SOUTH EAST ENGLAND
...submission strategy for clinical trials planned globally are in accordance with the overarching global regulatory strategy and any risks and issues are highlighted to the Global Regulatory Project Team (GRPT) and study teams within the development operations organization. /li li Ensure study...
Regulatory Affairs Coordinator
WINDSOR, ENGLAND, UNITED KINGDOM
...experience ideally in clinical trials and CTR submission experience would be preferred. Job Responsibilities include a portfolio of CTAs including preparation and distribution of documentation associated with new initial CTAs and all CTA maintenance activities such as substantial amendments...
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Account Manager - Clinical Trial Education
WINDSOR, ENGLAND, UNITED KINGDOM
Account Manager - Clinical Trial Education I'm recruiting for one of the most well known, global healthcare communications agencies looking for a unique position. They have a Clinical Trial Education team as well as their standard medical education, healthcare advertising and healthcare PR teams...
Regulatory Affairs Coordinator
WINDSOR, SOUTH EAST ENGLAND
...experience ideally in clinical trials and CTR submission experience would be preferred. /p p /p p b Job Responsibilities include; /b /p ul li a portfolio of CTAs including preparation and distribution of documentation associated with new initial CTAs and all CTA maintenance activities...
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We've expanded the search to "Berkshire" to find more jobs with all your keywords
Regulatory Specialist
MAIDENHEAD, ENGLAND, UNITED KINGDOM
...expertise for Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. Key Responsibilities: Manage a portfolio of CTAs including preparation and distribution of documentation...
Senior Biostatistical Programmer (Contractor)
READING, ENGLAND, UNITED KINGDOM
...experience within clinical trials. Experience with computerised information systems is preferred. Familiarity with ICH and local regulatory authority regulations in drug research and development is advantageous. Proficient in Microsoft Office applications, with a strong understanding of data...
Clinical Trial Operations Specialist
BRACKNELL
p strong CLINICAL TRIAL OPERATIONS SPECIALIST /strong /p p br br The following information aims to provide potential candidates with a better understanding of the requirements for this role. br /p p strong OUR COMPANY /strong /p p At Boehringer Ingelheim we develop breakthrough therapies...
Regulatory Specialist
MAIDENHEAD
...expertise for Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. /p p br /p p strong u Key Responsibilities: /u /strong /p p Manage a portfolio of CTAs...
Medical Advisor
READING
...product profile, and clinical data. /li li Stay abreast of the latest scientific developments, clinical trial data, and competitive landscape in the field of MS. /li li Collaborate with global and regional medical affairs teams to ensure alignment of medical strategies and activities. /li li...
Senior Biostatistical Programmer (Contractor)
READING
...experience within clinical trials. /li li Experience with computerised information systems is preferred. /li li Familiarity with ICH and local regulatory authority regulations in drug research and development is advantageous. /li li Proficient in Microsoft Office applications, with a...
Regulatory Specialist
MAIDENHEAD, SOUTH EAST ENGLAND
...expertise for Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. /p p br /p p b Key Responsibilities: /b /p p Manage a portfolio of CTAs including preparation and...
Senior Biostatistical Programmer (Contractor)
READING, SOUTH EAST ENGLAND
...experience within clinical trials. /li li Experience with computerised information systems is preferred. /li li Familiarity with ICH and local regulatory authority regulations in drug research and development is advantageous. /li li Proficient in Microsoft Office applications, with a...
We've expanded the search to "South East" to find more jobs with all your keywords
Global Clinical Operations Lead - Autoimmune
OXFORD, ENGLAND, UNITED KINGDOM
...to hire a new Global Clinical Operations Leader to help set this up and run the team. Although senior in title this is very much a hands on role and will be responsible for running the study. Summary The global/regional Clinical Operations Lead will oversee study execution and provide input as...
Medical Director - Global Clinical Development - Autoimmune
OXFORDSHIRE, ENGLAND, UNITED KINGDOM
...and execution of new clinical development assets across my client. They will be responsible for the strategy, medical oversight, direction and execution of the company s clinical development plans. This is a unique opportunity to be a major contributor to the success of well-positioned and...
Senior Clinical Project Manager
SURREY, ENGLAND, UNITED KINGDOM
Title: Senior Clinical Project Manager Salary: Highly Competitive Location: Surrey area (Hybrid) If you have a clinical background and are interested in joining an exciting international organisation then this could be the role for you! This company is a leading biotech with products on the market...
Head of Clinical Operations
OXFORD, ENGLAND, UNITED KINGDOM
Position Summary Hybrid role - 2/3 days on site in Oxford (flexibility offered) Salary - £120,000 - £140,000 Our start-up Biotech client are actively recruiting for a Head of Clinical Operations. This person will be accountable for the resourcing, development, training, and management...
Receptionist
MILTON KEYNES, ENGLAND, UNITED KINGDOM
About MRN Medical Research Network is an innovative market-leader of patient and site-centric solutions and clinical trial delivery. Through our integrated in-home, at-site and digital trial solutions, we allow the medical research community to create more flexible, efficient, and accessible...
Vice President Supply Chain
WEYBRIDGE, ENGLAND, UNITED KINGDOM
...plans. Experience in clinical trial labelling, supplies, logistics & distribution an advantage. Knowledge in planning, procurement and capacity a significant advantage. Exposure to Oracle ERP, Microsoft Office Suite, APICS Certification. This is an excellent opportunity to make an impact and be...
Manufacturing Technician
WITNEY, ENGLAND, UNITED KINGDOM
...Produce prototypes, pre-clinical, and clinical trial products in a cleanroom facility Conduct performance and product testing Maintain and calibrate equipment, ensuring cleanliness of the facility Contribute to process optimisation, risk management, and waste reduction Experience Needed: Basic...
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