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Senior Pharmacologist
, , UNITED KINGDOM
...capabilities across pharmacology. This position will report to the Bioassay Operations and Study Manager. Responsibilities include, but are not limited to: Designing, planning and conducting in vitro pharmacology studies to improve understanding of a drug's activity for CRO clients. Collect...
Associate Medical Director, Clinical Pharmacology, Leeds
78003
LEEDS, WEST YORKSHIRE, LEEDS, WEST YORKSHIRE
...of Fortrea s Clinical Pharmacology Services strategic objectives. Principal Investigator: You will ensure the proper conduct of studies and have primary responsibility for safety, health and welfare of clinical trial participants in Leeds. Representing Clinical Pharmacology as the medical...
Head of Research and Innovation
LONDON, ENGLAND, UNITED KINGDOM
...Medicine or Clinical Pharmacology Ability to work in the fast-paced but rigorous environment of a healthtech start-up Excellent communication skills with an ability to communicate complex science clearly and simply An interest in and understanding of female physiology, hormones, genetics and...
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Senior Pharmacologist
UNITED KINGDOM, UNITED KINGDOM
...capabilities across pharmacology. This position will report to the Bioassay Operations and Study Manager. /p p br /p p b Responsibilities include, but are not limited to: /b /p p br /p ul li Designing, planning and conducting in vitro pharmacology studies to improve understanding of...
Innovation Project Scientist/Manager
SURREY, ENGLAND, UNITED KINGDOM
...Chemistry, Pharmacy, Pharmacology, Biochemistry or Biological science 5+ years in FMCG or Healthcare Experience in science & Technology management/partnerships Excellent analytical skills, including strategic thinking Communication and influencing skills, ability to lead change...
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Postdoctoral Researcher – Biology MRC Nucleic Acid Therapy Accelerator
£39,375 - £41,843 a year
LONDON, ENG, GB
...the effective use and management of resources, training of others and taking responsibility for use of communal facilities br / br / Enhance your research and generic skills through a tailored development programme br / br / Present work internally and at national and international...
Sr. Medical Director, Prostate Cancer
BRENTFORD, ENGLAND, UNITED KINGDOM
...the development and management of clinical protocols and amendments, investigator brochures, and clinical study reports Provideleadership to medical directors and clinical scientists who lead the clinical study teams Oversee the evaluation of safety, pharmacology, and efficacy data from...
Senior Regulatory Affairs Associate
LONDON, ENGLAND, UNITED KINGDOM
...procedures and Quality Management System Oversee operational activities to support regulatory compliance Oversee the coordination of support agencies (e.g., regulatory publishing teams) and in-country regulatory experts. Communicate with health authorities when relevant Support product...
Head of Nonclinical Safety
UNITED KINGDOM, , UNITED KINGDOM
...reviews and budget management. Responsible for planning and developing study designs, outsourcing partner management/consultants, oversight of operational activities, results reporting and review of analysis and interpretation. Consolidating safety data from nonclinical studies into key...
Multilingual Medical Information Specialist - Norwegian Speaking
UNITED KINGDOM, , UNITED KINGDOM
...pathophysiology, pharmacology, regulations and industry standards. Strong cognitive abilities, including verbal reasoning, critical thinking and analytical ability. Ability to multitask with attention to detail within restrictive timeframes, including sound planning, prioritizing and...
Regulatory Manager, Clinical Trial Strategy & Submissions
, , UNITED KINGDOM
...Practices and Good Clinical Practices, ICH and other pertinent guidelines. Knowledge and experience of medical device legislation in relation to clinical trials is preferable. A Degree in medicine, pharmacy, biology, chemistry, pharmacology, or related life sciences subject is...
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...
Account Manager - Medical Communications
, , UNITED KINGDOM
...Science Jobs / Graduate Pharmacology Jobs / Graduate Pharmaceutical Jobs / Graduate Biology Jobs Our client, an established Medical and Healthcare Communications Agency in Hertfordshire, are looking for experienced candidates to join their team as an Account Manager to support the management of...
Assistant Sample Co-ordinator 1 1
23585
TRANENT, EAST LOTHIAN, TRANENT, EAST LOTHIAN
...support to study management in the co-ordination and reporting of their studies. Key Responsibilities: Prepare labels and apply to appropriate sample containers in preparation for scheduled sampling Preparing chain of custody in order to collect and transfer samples Preparing detailed...
Senior Director Human Resources
LONDON, ENGLAND, UNITED KINGDOM
We are looking for a Senior Director Human Resources (HR). to lead the UK Human Resources team and contribute to overall strategy and policy-making by advising the Management on human resource implications of its decisions. You will contribute as a senior manager within the Pharmaron UK management...
Principal Scientist / Senior Principal Scientist
LONDON, ENGLAND, UNITED KINGDOM
...should hold a PhD in pharmacology, chemistry, or a related subject. For the Principal Scientist role, experience of working in research laboratories (within industry or academia) and an understanding of drug development is highly desirable. For the Senior Principal Scientist role, we...
Head of Nonclinical Safety
UNITED KINGDOM, UNITED KINGDOM
...reviews and budget management. /li li Responsible for planning and developing study designs, outsourcing partner management/consultants, oversight of operational activities, results reporting and review of analysis and interpretation. /li li Consolidating safety data from nonclinical...
IP Litigation Associate
LONDON (CITY OF LONDON), SOUTH EAST ENGLAND
...UK litigation and the management of multi-jurisdictional litigation on a global scale. Litigation proceedings occur before esteemed bodies such as the General Court, Court of Appeal, High Court, IP Enterprise Court, and UK Intellectual Property Office (UKIPO). br b About You: /b br ul li IP...
Multilingual Medical Information Specialist - Norwegian Speaking
UNITED KINGDOM, UNITED KINGDOM
...pathophysiology, pharmacology, regulations and industry standards. /li li Strong cognitive abilities, including verbal reasoning, critical thinking and analytical ability. /li li Ability to multitask with attention to detail within restrictive timeframes, including sound planning...
Regulatory Manager, Clinical Trial Strategy & Submissions
UNITED KINGDOM, UNITED KINGDOM
...Practices, ICH and other pertinent guidelines. /li li Knowledge and experience of medical device legislation in relation to clinical trials is preferable. /li li br /li li A Degree in medicine, pharmacy, biology, chemistry, pharmacology, or related life sciences subject is required /li /ul...
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