Reference: PW 6483
Closing Date: 17 Mar 17
Salary (£): Competitive
Benefits: Competitive salary and health, life cover, pension
Quotient Clinical offers unique services – based on Translational Pharmaceutics® – that integrate formulation development, real-time drug product manufacturing and clinical testing, significantly reducing the time and cost of bringing a drug to market. For more than 20 years, Quotient Clinical has brought innovation to drug product development programs for pharmaceutical and biotechnology customers worldwide. The company is based in purpose-built, fully integrated facilities in the UK, encompassing formulation development, real-time GMP manufacturing and early clinical trials. It employs over 250 staff, offering a full range of support services, from study set-up right through to data analysis and reporting.
Quotient Clinical has driven substantial growth and will continue in a growth phase for the foreseeable future. To underpin and help drive this growth the company seeks to recruit a Medical Fellow (Associate Medical Director).
Reporting to the Medical Director, you will be responsible for the oversight of studies within a specific project team. This involves mentoring of the project team and management of a clinical research physician(s). You will also be responsible for the development and implementation of SOPs and ensure effective and (above all else) safe execution of clinical trials.
Through working effectively with other business functions (e.g. Pharmaceutical Operations, Data Sciences, Quality Assurance, Regulatory, Project Management and Business Development) you will support the Medical Director and Managing Director to ensure that the business achieves its key objectives and priorities.
You will act as Principal Investigator on an appropriate number and range of clinical trials
In this important and high profile role you will provide vision and leadership into new areas of medical science innovation consistent with the business’ strategic direction
QUALIFICATIONS / EXPERIENCE REQUIRED:
You will be medically qualified with full GMC registration. You will be able to demonstrate significant previous experience in the design and operational implementation of early-phase clinical trials and will hold the Diploma in Pharmaceutical Medicine or equivalent and have completed Higher Medical Training.
Importantly you will be an individual who is credible, dynamic, hardworking and who will work collaboratively with colleagues to deliver for the company and its clients – while always ensuring patient and volunteer safety. The business is growing and changing and will suit individuals who want to deliver within a non-hierarchical environment.
People join Quotient Clinical because they are a respected member of the drug development world, specialising in delivering innovative solutions that integrate formulation development, real time GMP manufacturing and clinical testing. They pride themselves on the quality of their services and their engaged culture. They are passionate about helping their customers get new medicines to market.
Learning and development is at the heart of the culture at Quotient and you will be given every opportunity to reach your potential with them. You’ll be recognised for your contribution and rewarded with genuine career development, a competitive salary & a whole host of benefits.
For a confidential discussion please telephone the retained consultant Jonathan Elliott at AXESS Limited on 020 8560 2300. To apply, please send your CV to firstname.lastname@example.org quoting reference PW 6483
Only candidates with EU work authorisation will be considered.
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AXESS has been operating since 1990
We are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory Affairs & Clinical Development
We match professional candidates to the best permanent, contract and interim roles in the market
Visit us at www.axess.co.uk
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