Medical Director - £80k
Basic: £80k
This established CRO has a presence in 30 countries worldwide and full service capabilities from phase I-IV and expertise in handling a wide range of studies from paediatrics to geriatrics.
A medically qualified, GMC registered professional is required to take on Medical Director responsibilities within the UK on an international level. Responsibilities will include: review and sign off of all CTX applications made on behalf of clients, review all pre-clinical and clinical information on a drug or compound before study initiation, assisting with the preparation of ethics committee applications and attend LREC/MREC meetings when required. You will also assist with business development and proposal activities, specifically to co-ordinate feasibility work. As a senior medical representative you will also liaise with regulatory, safety and senior management to provide medical input into business plans and project strategy.
You will have a minimum of three years experience within clinical research - preferably within the CRO environment - as a research physician or medical director. In depth knowledge of preclinical and clinical drug development is essential. A competitive remuneration package is available including relocation assistance.
More Info / Apply
This established CRO has a presence in 30 countries worldwide and full service capabilities from phase I-IV and expertise in handling a wide range of studies from paediatrics to geriatrics.
A medically qualified, GMC registered professional is required to take on Medical Director responsibilities within the UK on an international level. Responsibilities will include: review and sign off of all CTX applications made on behalf of clients, review all pre-clinical and clinical information on a drug or compound before study initiation, assisting with the preparation of ethics committee applications and attend LREC/MREC meetings when required. You will also assist with business development and proposal activities, specifically to co-ordinate feasibility work. As a senior medical representative you will also liaise with regulatory, safety and senior management to provide medical input into business plans and project strategy.
You will have a minimum of three years experience within clinical research - preferably within the CRO environment - as a research physician or medical director. In depth knowledge of preclinical and clinical drug development is essential. A competitive remuneration package is available including relocation assistance.
More Info / Apply


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