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As a Regulatory Affairs Manager you will provide leadership in the introduction and the development of new and existing markets globally, ensure all regulatory and quality systems are in place are maintained and established along with accurate decisions made within scope of the role.
As a Regulatory Affairs Manager you will provide leadership in the introduction and the development of new and existing markets globally, ensure all regulatory and quality systems are in place are maintained and established along with accurate decisions made within scope of the role.
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As a Regulatory Affairs Manager you will provide leadership in the introduction and the development of new and existing markets globally, ensure all regulatory and quality systems are in place are maintained and established along with accurate decisions made within scope of the role.
As a Regulatory Affairs Manager you will provide leadership in the introduction and the development of new and existing markets globally, ensure all regulatory and quality systems are in place are maintained and established along with accurate decisions made within scope of the role.
Senior Medical Advisor / Medical Affairs - Southampton, HampshireMedical Advisor / Medical Affairs to join a global pharmaceutical company. As Senior Medical Advisor / Medical Affairs you will be offered a salary of c75k + car.
Director of Medical Affairs - Germany, Non UKBerkley Pharma & Life Sciences are currently seeking a Director of Medical Affairs for our leading pharmaceutical development client based near Hamburg, Germany.Role/Opportunity:To act as the clinical expert for the Dermatology team and be aware of current issues and developments within Dermatology.
Are you looking for a leadership role with a blue chip pharmaceutical company's oncology team. My client is recognised as one of the world's top research driven pharmaceutical companies with a huge number of compounds scheduled for launch over the next 5 years.
As the Senior Director Medical Affairs you will work as an internal consultant in the planning, designing and accomplishing of key projects to improve medical business performance as well as provide leadership and technical expertise within the medical organisation influencing conceptual methodology.
Responsible for the provision of medical affairs support to the sales, marketing and regulatory teams in OU UK & Ireland to ensure we meet/exceed our targets and we are compliant with all relevant legislation and codes of practice.
Job Description Provides a single point of Medical department leadership for the Therapeutic Area Team in respect to currently marketed and development products. Lead and manage allocated resources, budget and CDA team in all aspects of local Oncology medical/scientific activities.
A Successful candidate must have experience working within a regulatory environment; have knowledge of Medical Devices products. Experience in preparing and submitting 510K applications, knowledge of cGMP, FDA & PMA. Show the ability to demonstrate initiative and attention to detail, good organisational skills and the ability to work to deadlines across multiple simultaneous projects.
The role of a medical writer with this company will be varied and exciting. There are opportunities to be client facing as you take briefings at meetings. You will take a lead in managing projects and as well as writing, you will review junior writers work.
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