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Clinical Research Associate
OXFORDSHIRE, ENGLAND, UNITED KINGDOM
Cure Talent are delighted to be partnered with an established Medical Devices Manufacturer, who, due to their continued growth, have an exciting opportunity for an experienced Clinical Research to join them. As the new Clinical Research Associate, you will be responsible for overseeing trial sites...
Associate Director Regulatory Affairs
LONDON, ENGLAND, UNITED KINGDOM
Job Description Job Title: Associate Director, Regulatory Affairs Main Purpose of Role: The Associate Director, Regulatory Affairs, plays a pivotal role in providing strategic regulatory and scientific support for pre-clinical and clinical development plans. Collaborating with Regulatory Affairs...
Clinical Research Associate
OXFORDSHIRE, SOUTH EAST ENGLAND
p Cure Talent are delighted to be partnered with an established Medical Devices Manufacturer, who, due to their continued growth, have an exciting opportunity for an experienced Clinical Research to join them. /p p br /p p As the new Clinical Research Associate, you will be responsible for...
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Senior Product Manager
£100 - 125
LONDON
...trusted platform for clinical development, commercial, and real-world data. Known for its ground-breaking technological innovations, Medidata has supported more than 30,000 clinical trials and 9 million study participants. And Medidata's ongoing commitment to infusing the patient voice into...
Associate Director/Clinical Trial Lead
UNITED KINGDOM, , UNITED KINGDOM
Remote UK Multinational Pharma Salary D.o.E + Benefits The Company Carrot is partnering with a Global Pharmaceutical company focused on finding novel and vibrant ways of advancing healthcare. They are on the search for a new Associate Director to manage the end-to-end clinical trial process...
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Regulatory Manager, Clinical Trial Strategy & Submissions
, , UNITED KINGDOM
We re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid. The Role: Deliver CTA...
Clinical Trial Assistant
LONDON AREA, UNITED KINGDOM, UNITED KINGDOM
Role: Clinical Trial Assistant (CTA / Associate CPM) Location: Hybrid (4 days remote and 1 day per week in London) Company: Small Biopharmaceutical Company Salary: £35,000 - £42,000 (depending one experience) RBW Consulting are excited to announce an exciting opportunity to join a...
Clinical Research Associate
SWANSEA, WALES, UNITED KINGDOM
...the progress of clinical trials and research endeavours. You will ensure that all research activities are meticulously conducted, documented, and reported in strict adherence to Protocols, SOPs, ICH-GCP guidelines, and relevant regulatory mandates. Moreover, you will provide a...
Clinical Negligence Associate
, , UNITED KINGDOM
About the Job We are pleased to present this unique opportunity to join a Top Tier Legal 500 Firm in London. Clinical Negligence - Solicitor - London - Salary DOE The Role This is a rare opportunity to join a Top Tier Legal 500 Firm that offers specialist quality legal advice to individuals...
Regulatory Affairs Associate (EU)
SURREY, ENGLAND, UNITED KINGDOM
Regulatory Affairs Associate The Regulatory Affairs Associate will be responsible for: Managing the clinical trial applications in Europe and other selected countries Keeping up to date with regulatory and legal changes in EU Preparing pre- and post-authorisation regulatory documentation and...
Associate Clinical Project Manager
, , UNITED KINGDOM
Advanced analytics. Intelligent insights. IXICO plc (AIM: IXI), is a leading neuroimaging Contract Research Organization (CRO), delivering advanced Ai analytical insights in neuroscience to the global clinical trials market. Established in 2004, listed as a public company in 2013, IXICO has firmly...
Associate People Manager - Laboratory - Ireland
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
Associate Group Leader Laboratory - Ireland Onsite role located in County Roscommon, Ireland. Relocation Assistance. Visa sponsorship available. At PPD, part of Thermo Fisher Scientific, you ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in...
Principal Consultant, Clinical
, , UNITED KINGDOM
The Company Scendea is a leading product development and regulatory consulting practice serving the pharmaceutical and biotechnology industry. Scendea s international team offers strategic and operational support in the fields of CMC, nonclinical/toxicology, clinical/medical and regulatory, which...
Associate Market Access Consultant
LONDON AREA, UNITED KINGDOM, UNITED KINGDOM
Blackfield Associates are currently supporting a growing and bespoke management consultancy, working across the healthcare and life sciences markets, coming health expertise with innovative approaches from their work. They launched their HEOR & Market Access group in 2020, providing analytical and...
Senior R&D QA GCP Auditor
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
Background must be in pharma NOT medical devices) Senior R&D QA GCP Auditor (pharmaceuticals) I'm looking to recruit a seasoned Senior R&D QA GCP Auditor responsible for ensuring compliance and proper implementation of Good Clinical Practice (GCP) and Good Clinical Laboratory Practice (GCLP) within...
Business Development Associate
HEMEL HEMPSTEAD, ENGLAND, UNITED KINGDOM
Business Development Associate Location: Hemel Hempstead Working Hours: Monday Friday, 9am 5:30pm 1 hour for lunch. Total working hours : 37.5 hours Company operates Flexible Working Times Arrive anytime from 8:30hrs 10:00hrs and finish any time after 16:00hrs Salary: Dependent on...
Associate Director/Clinical Trial Lead
UNITED KINGDOM, UNITED KINGDOM
...on the search for a new Associate Director to manage the end-to-end clinical trial process. This person will have significant project management experience and be able to hit the ground running in a dynamic and energetic global team. /p p br /p p br /p p The Role /p p br /p p The...
Regulatory Manager, Clinical Trial Strategy & Submissions
UNITED KINGDOM, UNITED KINGDOM
p We’re currently recruiting for a Regulatory Clinical Trial Strategy & Submissions Manager for a Global Pharmaceutical Company who have opened a new vacancy within their Regulatory Affairs team on an initial 12 Month basis to be based at their office in Maidenhead/hybrid. /p p br /p p b...
Clinical Trial Assistant
LONDON, SOUTH EAST ENGLAND
ul li Role: Clinical Trial Assistant (CTA / Associate CPM) /li li Location: Hybrid (4 days remote and 1 day per week in London) /li li Company: Small Biopharmaceutical Company /li li Salary: £35,000 - £42,000 (depending one experience) /li /ul p br /p p RBW Consulting are...
Clinical Research Associate
SWANSEA, SWANSEA
...the progress of clinical trials and research endeavours. You will ensure that all research activities are meticulously conducted, documented, and reported in strict adherence to Protocols, SOPs, ICH-GCP guidelines, and relevant regulatory mandates. Moreover, you will provide a...
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