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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...
Clinical Trial Specialist Apprentice
FARNBOROUGH, HAMPSHIRE, FARNBOROUGH, HAMPSHIRE
Description Clinical Trial Specialist Apprentice Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our...
External Data Manager
UNITED KINGDOM, , UNITED KINGDOM
Planet Pharma are currently partnered with a top 10 pharmaceutical company who are seeking a External Data Manager to join the external data team and oversee and support the day to day operations of the company s drug portfolio. This is a home based position with HQ in the UK (However we are open...
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Head Of Clinical Data (Healthtech/Clinical Trials)
LONDON, ENGLAND, UNITED KINGDOM
Overview The Clinical Data Lead holds a pivotal role within a Series A healthtech/clinical trials company, requiring a candidate with a medical background. They will spearhead the establishment and management of crucial clinical data contracts with hospitals, both domestically and internationally...
External Data Manager
UNITED KINGDOM, UNITED KINGDOM
p Planet Pharma are currently partnered with a top 10 pharmaceutical company who are seeking a External Data Manager to join the external data team and oversee and support the day to day operations of the company’s drug portfolio. /p p /p p This is a home based position with HQ in the UK...
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Head of Clinical Data (Healthtech/Clinical Trials)
LONDON, ENGLAND, UNITED KINGDOM
Overview The Clinical Data Lead holds a pivotal role within a Series A healthtech/clinical trials company, requiring a candidate with a medical background. They will spearhead the establishment and management of crucial clinical data contracts with hospitals, both domestically and internationally...
Maternity Sales Specialist
BIRMINGHAM, WEST MIDLANDS (COUNTY)
MATERNITY SALES SPECIALISTNATIONAL/ BIRMINGHAM£55K + CA + 30% BONUSSUMMARYOur global medical devices client is looking for an experienced Maternity Sales Specialist with a clinical or sales background in maternity. This role will work with current Sales, clinical and marketing team in...
Senior Clinical Data Manager - FSP (oncology experience)
58481
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 Clinical Data Manager - single sponsor
41408
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...
Head of Clinical Data
CAMBRIDGE, ENGLAND, UNITED KINGDOM
The Head of Clinical Data is a key senior position within the company. It is for an individual who must be a medically trained doctor and who will be responsible for creating and maintaining clinical data contracts with hospitals both in the NHS and abroad and who will be the key person partner in...
Senior Specialist, CPSO Drug Product Dispensary Operations
40370
NEW BRUNSWICK, NEW JERSEY, UNITED STATES OF AMERICA, , NEW BRUNSWICK, NEW JERSEY, UNITED STATES OF AMERICA,
...working-with-us . Our Clinical Supply Operations is responsible for the supply of drug product administered to patients in clinical studies worldwide. In Global Product Development and Supply the team works closely with our partners to deliver quality products safely, efficiently and on time...
Senior Clinical Quality Assurance Specialist
, , UNITED KINGDOM
...Quality Assurance Specialist to join their team. This successful candidate will be reporting to the Senior Clinical Quality Assurance Manager coordinate the implementation of the company quality management system relevant to GCP (including laboratory analysis of clinical samples) including...
Head of Regulatory Affairs
UNITED KINGDOM, , UNITED KINGDOM
...enhancing treatment and clinical results for patients living with cancer. Our client is seeking a dynamic leader to provide strategic input and leadership to project teams in support of developmental through to post-approval commitments. Discover more about our Head of Regulatory Affairs...
Senior Research Physician
35821
MERTHYR TYDFIL, , MERTHYR TYDFIL (MERTHYR TUDFUL), MERTHYR TYDFIL, UNITED KINGDOM, MERTHYR TYDFIL (MERTHYR TUDFUL)
ABOUT US Simbec-Orion is a responsive and agile full-service CRO, with wide therapeutic experience and specialist expertise in clinical pharmacology, oncology and rare diseases. Perfectly structured, we provide full-service clinical development solutions for small and mid-size drug developers...
Associate Director - Quality Assurance
, , UNITED KINGDOM
...high level specialist expertise to both the A team and key stakeholders in relation to this manufacturing site. The role has responsibility for building and managing a small team of A professionals and creating a strong quality culture on the site. The individual will deputise for...
Senior Biostatistician (Remote)
LONDON, ENGLAND, UNITED KINGDOM
...design. Review study database structures, edit checks, and data management coding convention. Prepare statistical analysis plans, including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports. Conduct statistical...
Senior Statistician, Oncology (Remote)
LONDON, ENGLAND, UNITED KINGDOM
...design. Review study database structures, edit checks, and data management coding convention. Prepare statistical analysis plans, including the definition of derived data, and the design of statistical tables, figures, and data listings for clinical summary reports. Conduct statistical...
Director Regulatory Affairs
, , UNITED KINGDOM
...possible approvals of clinical trials and marketing authorization applications. What you will do: As the Regulatory Affairs Director, your duties and responsibilities will include: Managing all aspects of submissions relevant to assigned projects and programs, in accordance with submission and...
TMF Lead II (office-based)
48840
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...
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