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Translational Medicine/Clinical Pharmacology Pharmaceutical Physician
UNITED KINGDOM, , UNITED KINGDOM
An opportunity has arisen for an experienced drug development pharmaceutical physician with strong clinical pharmacology and translational medicine skills with a history of being part of successful teams and ready to develop the next stage of their career in the new world of pharmaceutical...
Senior Medical Director - CNS/Neurology - Europe - Home-based
LONDON, ENGLAND, UNITED KINGDOM
Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications from discovery to reality. Anchored in our company s scientific...
Translational Medicine/Clinical Pharmacology Pharmaceutical Physician
UNITED KINGDOM, UNITED KINGDOM
p An opportunity has arisen for an experienced drug development pharmaceutical physician with strong clinical pharmacology and translational medicine skills with a history of being part of successful teams and ready to develop the next stage of their career in the new world of pharmaceutical...
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Diriector of Project Delivery, Europe
£100 - 125
GREATER LONDON
...s with name changed to Pharmaceutical Research Associates Inc., in 1981 with focus on data management in Virginia, USA. /li li In 1991, PRA expanded its service offering to include clinical trial management and opened their first European location. /li li 1996 saw the company name change to PRA...
Head of Field Medical Affairs
LONDON, ENGLAND, UNITED KINGDOM
CSL Vifor is a world leading pharmaceutical company focused on Nephrology, Iron Deficiency and Cardio-Renal therapies. At this time we are seeking to add to our medical affairs leadership in the UK with a Head of Field Medical Affairs UK. In this position reporting to the UK Medical Director, you...
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Associate Director, Clinical Pharmacology
BROOKLANDS, UNITED KINGDOM
...lead preparation of the Investigator s Brochure and clinical study reports, CTD modules, answers to HA questions. Supervises study setup (in co-operation with Clinical Operations and other study team members review of Task orders and deliverables) and study execution (Kick-off meeting Site...
Clinical Trials Principal Investigator - Christchurch, New Zealand - Great Salary & Relocation Package - Suitable for UK & IE doctors - New Zealand
£128,787 - £166,946
UK
The Position An exciting opportunity for a Clinical Trials Principal Investigator in Christchurch, New Zealand. The Principal Investigator (Early Phase) provides medical, scientific, and strategic leadership to the organisation through the identification, selection, and execution of suitable...
Medical Science Liaison (Inflammation)
, , UNITED KINGDOM
...Opinion Leaders (KOLs), investigators and other stakeholders in patient care, establish strong professional relationships, provide credible scientific expertise and serve as a liaison to Global Medical, Global Clinical and external partners Ensures high standard of professionalism to develop and...
Clinical Project Manager (Remote)
, , UNITED KINGDOM
...of protocols, Investigator Brochures, scientific review of clinical data, and study data analysis, reporting and publishing Selects manages and oversees clinical study vendors / CROs, including preparation of recommendations for the selection a (i.e. RFP, bid requests, proposal reviews...
Clinical Research Physician
CANNOCK, ENGLAND, UNITED KINGDOM
...fulfil the role of Sub-Investigator and Principal Investigator in clinical research studies in compliance with the protocol and ICH/GCP. KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED: Full and current GMC registration (essential) 4 years post-graduation experience (desirable) MRCP /MRCGP...
CRA II/ SCRA - Fast career development
CITY OF LONDON, ENGLAND, UNITED KINGDOM
...in the Life: Monitors investigator sites with a risk-based monitoring approach applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data...
Principal Scientist: Pharmacometrics
ALDERLEY EDGE, ENGLAND, UNITED KINGDOM
Are you a Pharmacometrics expert looking to make your mark across the pharmaceutical sector whilst working for a well renowned, exciting CDMO focused on solving complex pharmaceutical problems for their customers? Job Title: Principal Scientist - Pharmacometrics Expert Type: Permanent Salary...
Head of Nonclinical Safety
UNITED KINGDOM, , UNITED KINGDOM
...documents, such as Investigator s Brochures, briefing books, safety updates and submission dossiers. Interacting and seeking input from external partners/experts. Requirements include: PhD or equivalent degree in the areas Toxicology or Pharmacology, with 10+ years related experience...
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...
Clinical Project Director
, , UNITED KINGDOM
...Plan and present at Investigator meetings. Lead the operationalisation of the clinical development plans and development and implementation of clinical project plans. Participate in the development, review, and implementation SOPs. Participate in vendor, site and CRO audits and conduct...
Regulatory Affairs Associate (EU)
SURREY, ENGLAND, UNITED KINGDOM
...with updating the Investigator Brochure and Investigational Medicinal Product Dossier Assist in the development of the ongoing global regulatory strategy Submissions of marketing authorisation applications and variations Prepare response to questions raised by competent authorities...
Associate Director, Clinical Trial Management
UNITED KINGDOM, , UNITED KINGDOM
...including protocol, investigator brochure, informed consent, etc. Participate in Case Report Form design and user acceptance testing in partnership with Data Management as well as data monitoring over the course of the study. Oversee study management and/or clinical development teams (CROs) to...
Clinical Research Physician
CANNOCK, MIDLANDS
...fulfil the role of Sub-Investigator and Principal Investigator in clinical research studies in compliance with the protocol and ICH/GCP. /p p br /p p b KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED: /b /p ul li Full and current GMC registration (essential) /li li 4 years...
Medical Science Liaison (Inflammation)
UNITED KINGDOM, UNITED KINGDOM
...Opinion Leaders (KOLs), investigators and other stakeholders in patient care, establish strong professional relationships, provide credible scientific expertise and serve as a liaison to Global Medical, Global Clinical and external partners /li li Ensures high standard of professionalism to...
CRA II/ SCRA - Fast career development
LONDON (CITY OF LONDON), SOUTH EAST ENGLAND
...the Life: br Monitors investigator sites with a risk-based monitoring approach applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. br Ensures...
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