CLINICAL AND REGULATORY PRODUCT jobs in United Kingdom #5

and Systems Manager - Clinical Trials / Real World Evidence at Reckitt, you'll have the freedom to drive innovative product... and Systems Manager - Clinical Trials / Real World Evidence at Reckitt, you'll have the freedom to drive innovative product...

Reckitt Benckiser

/ source document review (SCV), regulatory documents, and investigational product. Experience/Qualifications Independent... of all investigational product(s) and trial-related material. Participate and act as Lead CRA on studies where you can add assistance...

Global Life Science Hub

range of regulatory matters such as advising the business on compliance with new laws and regulations impacting e-commerce, such as the... Digital Services Act, Online Safety Bill, and the General Product Safety Regulation. The ideal candidate will have 4-7 years...

Taylor Root

, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres..., always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring...

Reckitt Benckiser

differentiation and value What You’ll Do Drive innovative product launches to successfully introduce products in new markets... Driving adoption with clinical workflow support tools partnering with UK consultants facilitating patient pathway improvement...

Abbott

Product Surveillance Reporting Analyst 12 months £17.96 p/h Marlow - hybrid (3 days on site) SRG are partnered... with a pharmaceutical organisation who are seeking a Product Surveillance Reporting Analyst to join their team in Marlow. Purpose of the...

SRG

industry or in a clinical setting (preferred) Knowledge of global regulatory requirements for pharmaceutical, medical devices...SRG are partnered with a pharmaceutical organisation who are seeking a Product Surveillance Reporting Analyst...

SRG

therapeutic options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage....com and follow @JazzPharma on Twitter. Brief Description: This position resides in New Product Planning-Partnerships, reporting...

Jazz Pharmaceuticals

. We enable researchers and decision-makers to discover evidence from millions of academic publications, clinical trials..., regulatory documents, patents and other data sources… in minutes. Using our AI technology, we are developing the world...

Causaly

. We enable researchers and decision-makers to discover evidence from millions of academic publications, clinical trials..., regulatory documents, patents and other data sources… in minutes. Using our AI technology, we are developing the world...

Causaly

Position: Product Quality Assurance Analyst Location: Dundee Salary: 13.59£ ph Hours: Mon to Fri - 37.5 pw The... Role: The position of Product Quality Assurance Analyst is within Abbott's Cardiometabolic and Informatics Business Unit...

Randstad

experience in the biopharma industry, regulatory agency, clinical research or other related healthcare environment, including... into product development and lifecycle management as well as perform or oversee other advanced MSS activities...

Gilead

functionality, product quality, reliability, serviceability, manufacturability, regulatory, compliance, and cost. To act...Head of Product Development based in North Yorkshire. Working for a well established R&D Organisation...

Michael Page

Work Flexibility: Field-based Provide clinical product support to all end users and provide on-site guidance... and company's regulatory department detailing case reviews, services performed and recommendations for product, documentation...

Stryker

with ≥1 years industry experience within either product development, clinical trials or research. Strong communication... for an experienced and professional Senior Product Development Scientist to join our Research and Development team at head office in...

Tangerine Holdings

in clinical or preclinical therapeutic areas Leading the delivery and oversight on a multiple studies/indication... to the delivery of studies, development plans, regulatory strategy, health technology assessment and/or commercial activities...

Clinical Professionals

with complaints management within the organization, like affiliate CQA, Medical Information, Regulatory Affairs and Pharmacovigilance... · Supports more complex complaints that are escalated. · Serve as a Subject Matter Expert for a designated product...

Clinical Professionals