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Principal Regulatory Medical Writer
£50,000 - £58,000 per annum
LONDON
...that of a medium-sized pharmaceutical company, spanning antibodies, cell therapies, vaccines, drug conjugates and small molecules, making this an interesting and dynamic area to work in. /p br br p strong What will I be doing? /strong /p br br p You'll provide medical writing expertise...
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...
Senior Project Clinical Data Manager
52679
LONDON (GREATER), LONDON (GREATER), LONDON (GREATER), LONDON (GREATER)
...third-party, and investigator meetings or seminars Development of departmental strategies, technologies, SOPs and process Develop and delivery of applicable data management training Support departmental management by training, developing and mentoring of data management staff Maintain...
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Start up Line Manager London
LONDON, ENGLAND, UNITED KINGDOM
Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Start up Line Manager in London...
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...
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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...
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...
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...
Risk Based Quality Manager
NOTTINGHAMSHIRE, ENGLAND, UNITED KINGDOM
CK Group a recruiting for a Risk Based Quality Manager to our client on a permanent based at their midlands based site. Our client are a global pharmaceutical company that have a core focus on oncology, respiratory and neurological disorders. What they are looking for some to have the...
Senior Medical Science Liaison
UNITED KINGDOM, , UNITED KINGDOM
...site identification, investigator meetings, and protocol education. Gather insights from interactions with healthcare professionals to inform internal teams about market trends, competitor activities, and unmet medical needs. Collaborate with cross-functional teams, including medical affairs...
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...
Senior Clinical Trial Manager
, , 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...
Principal Regulatory Writer
UNITED KINGDOM, , UNITED KINGDOM
Job Opportunity: Principal Regulatory Writer (Remote) About Us: We are a dynamic and growing medical communications agency committed to excellence in pharmaceutical communications. As we expand our clinical/regulatory department, we are actively seeking a talented and experienced Principal...
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...
Sr. Medical Science Liaison Rare Disease UK
44915
, UNITED KINGDOM,
...Health is a pure-play pharmaceutical commercialization company helping clients navigate the road from product to patient. We strive to ensure patients gain access to and benefit from the best medicines for the right reasons, using our EPIIC values (excellence, passion, integrity, innovation and...
Medical Director
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
...Draft protocols, investigator brochures, and clinical study reports, while also reviewing trial documents. Facilitate investigator meetings and site initiation visits, fostering collaboration with clinical trial investigators. Develop and execute drug development strategic plans, offering...
Director, Clinical Development Scientist, Oncology
72992
(GB), , UNITED KINGDOM (GB),
...protocol development, investigator brochures, CRFs, clinical study reports, review of documents, study analyses and reporting. Provide expertise to cross-functional team members to synthesize/contextualize data to facilitate timely decision making. Serve on the clinical sub-team supporting...
Senior Director, Lead Clinical Development Scientist, Immuno-Oncology
77401
(GB), , UNITED KINGDOM (GB),
...protocol development, investigator brochures, CRFs, clinical study reports, review of documents, study analyses and reporting. Provide expertise to cross-functional team members to synthesize/contextualize data to facilitate timely decision making. Serve on the clinical sub-team supporting...
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