Clinical Pharmacology Scientist

£60000 - £70000 per annum
  1. Permanent
London
  1. Medical, Medical Communication
Posted: 24/09/2021
BBBH17318

This vacancy has now expired. Please see similar roles below...

A fantastic vacancy has become available for a Clinical Pharmacology Scientist to join a leading consultancy who deliver clinical excellence from design to delivery. This role will be located in London with remote working available and will be on a permanent basis.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

  • Ensure effective scientific document writing and quality control processes are implemented and maintained in order to meet all regulatory requirements to gain timely approval for studies.
  • Drive collaboration and innovation within the Advanced Research Science team as well as cross-functionally by implementing continuous process improvements.
  • Provide essential quality control (QC) processes to the Advanced Research Science team and optimisation of clinical documents concurrently across a number of studies.
  • Ensure all departmental documentation created internally as well as outsourced documents are filed appropriately and ready for inspection and audit and address relevant inspection, audit and CAPA items.
  • Assist senior team members in managing and developing entry level positions into the advanced research science department to gain experience and competency in the departmental tasks.

Key Skills:

  • Strong communication skills, both written and verbal required to articulate concepts and ideas and to suit the level of understanding of the target audience including patients, physicians or regulators.
  • Driven, persuasive and able to influence and have an impact at all levels of the organisation, bringing innovation and enthusiasm to drive process improvement.
  • Experience and ability to manage outsourced writing activities and collaborations with other CROs and service providers.

Requirements:

  • BSc in Clinical Pharmacology or other life Science.
  • Strong record of compiling clinical trial documents (at least 3 years).
  • Advanced level of knowledge of all relevant industry guidance and standards (e.g. FDA, EMA, ICH, PMDA).
  • Evidence of implementation of new processes and information in relation to best practices and standards, as well as emerging pharmaceutical industry guidance, enabling our advanced research science processes to remain leading edge and competitive.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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