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Principal Regulatory Medical Writer
£50,000 - £58,000 per annum
LONDON
...and precision medicine clinical trials in oncology agents. Our broad portfolio rivals 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...
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...
Sr. Medical Science Liaison Rare Disease UK
44915
, UNITED KINGDOM,
...both Medical Affairs & Clinical Development objectives for the portfolio of pipeline products in rare disease. You will serve as a key interface with clinical trial sites across all development programs, working closely with Clinical Development and Clinical Operations. Additionally, you will...
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Research Psychiatrist
GREATER LONDON, ENGLAND, UNITED KINGDOM
Division: Clerkenwell Health Clinical Research Facility (CRF) Reporting to: Clinical Director Role Type: Permanent with a 3-month probationary period Availability: 3 days per week with the possibility of expanding to full time. Some weekend working if applicants agree to this, but this is not...
Principal Consultant, Clinical
UNITED KINGDOM, UNITED KINGDOM
...nonclinical/toxicology, clinical/medical and regulatory, which guide products efficiently from early development to marketing approval. /p p With a current team of over 50 staff based in the UK, Australia, the Netherlands, and the US, Scendea is undergoing a period of significant growth, with the...
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Aspiring Clinical Psychologist
LEATHERHEAD, SURREY
...Start date ASAP, trial days taking place to ensure the role and school is right for you Excellent on-site training, support and CPD is provided £80-£85 per day, Mon-Fri, 08:30 to 16:30, PAYE, term time only No previous experience is required GCSE in English and...
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 Study Lead (maternity leave)
UNITED KINGDOM, , UNITED KINGDOM
Oxford Global Resources is hiring a Clinical Study Lead ( IVD experience is a must ) for temporary maternity leave. As a Clinical Study Lead/Trial Manager you will be responsible for the development and execution of all study associated documentation including protocols, investigator brochure...
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...
Principal Biostatistician
UNITED KINGDOM, , UNITED KINGDOM
...to advance the state of clinical development. Who Are You? An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will lead one Phase I-IV clinical studies across your region. You are excited and...
Field Manager - International Medical Solutions - Amplity Health
, UNITED KINGDOM,
...challenges Clinical & Medical Outsourced Solutions - Building end to end external engagement solutions and capabilities across clinical and medical affairs globally Consulting - Building end to end external engagement solutions and capabilities across clinical and medical affairs...
Medical Monitor
ENGLAND, UNITED KINGDOM, UNITED KINGDOM
MAC Clinical Research are looking for an experienced Medical Monitor to join their growing CRO team! This is an exciting opportunity to work on projects with sponsor companies in our Medical Monitoring Department. Qualifications Medical doctor degree 2 years experience in pharmaceutical industry...
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 Research Nurse
£36/hour Paid travel time, mileage, expenses
LONDON, EC1
Clinical Research Nurse PCM TRIALS provides quality, in-home clinical trial visits for our Sponsors and CROs partners. We're the only company that hires, certifies, tests, manages and trains our own Certified Mobile Research Nurses (CMRNs) in study protocol standards. Our mission is to bring...
Principal Clinical RA Consultant - Focus on Innovation
45280
NORTH HOLLAND, AMSTERDAM, NETHERLANDS, , NORTH HOLLAND, AMSTERDAM, NETHERLANDS,
Our client, a growing international biotech consultancy, is expanding its team in The Netherlands and looking for a Principal Clinical RA Consultant. As part of the starting group in the Netherlands, you will witness positive changes firsthand and have the opportunity to grow with the company...
TMF Manager
69043
READING, LONDON (GREATER), READING, LONDON (GREATER)
Job Purpose Responsible for efficient and appropriate management of Trial Master Files (TMF) and other TMF related, inspection relevant documents from creation through archival in compliance with applicable SOPs, processes and study specific requirements for assigned trials according to established...
Study Start-Up Project Manager (Ethics and Regulatory Submissions)
63451
MAIDENHEAD, BERKSHIRE, MAIDENHEAD, BERKSHIRE
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions...
Senior Site Activation Specialist (contract negotiator)
37623
WARSAW, , WARSAW,
Senior Site Activation Coordinator (Contract Negotiator) Country Site Activation Join us on our exciting journey IQVIA s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective...
Clinical Study Lead (maternity leave)
UNITED KINGDOM, UNITED KINGDOM
p Oxford Global Resources is hiring a Clinical Study Lead ( b IVD experience is a must /b ) for temporary maternity leave. /p p br /p p As a Clinical Study Lead/Trial Manager you will be responsible for the development and execution of all study associated documentation including protocols...
Diriector of Project Delivery, Europe
£100 - 125
GREATER LONDON
PRA International is one of the world’s leading Global Clinical Research Organisations. p With an established presence, spanning more that 30 years, they have enjoyed continual growth and success, currently employing 3,200 staff globally. /p p PRA have managed to continually build and...
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