Matching 33 Business development pharmaceutical jobs in Cambridgeshire

...to late-stage clinical development services for the world's biopharmaceutical, pharmaceutical & medical device industry. As the Clinical Project Manager you will be responsible for customer satisfaction & lead the project team members and achieve overall financial goals... click here for more details »

...aspects of the business, but will also be involved in some business development and general office organisation tasks. The Role Reporting to the Regulatory Affairs Manager you will offer technical knowledge of regulatory services including Clinical Trial... click here for more details »

...to late-stage clinical development services for the world's bio pharmaceutical industry. As the Principal Regulatory Consultant you will be responsible for providing advice and assistance to clients and other associates in their areas of expertise. You will work closely with... click here for more details »

...aspects of the business, but will also be involved in some business development and general office organisation tasks. The Role Reporting to the Directors of the company you will act as the prime contact for the management of clinical projects along with the... click here for more details »

Flame Pharma Regulatory Affairs - Regulatory Affairs Manager Job - Europe: Job Summary Would you like to work with one of the largest companies in the pharmaceutical services sector? Would you like to use your knowledge and expertise on various projects? An opportunity has... click here for more details »

...on contributing to the development of important therapies. This role will require the very best within the Clinical Research sector and as a result, the salary and benefits package are reflective of this. Teamwork and commitment will be rewarded and you will receive full... click here for more details »

...be responsible for the development and optimisation of the Quality Management Systems processes in response to changing business and regulatory requirements. THE PERSON: You will have proven medical device industry experience, preferably within a Quality Management Systems... click here for more details »

...be responsible for the development, maintenance and implementation of test cases and scripts for both the GUI and back-end of real-time semantic search software. You will review feature requirements, produce test plans and carry out testing and analysis of the results on... click here for more details »

...Good experience in pharmaceutical/biotechnology safety Knowledge Understanding of global regulatory requirements for pharmacovigilance Clinical knowledge of therapeutic area patient populations and drug class Proficiency in technical safety systems including ARISg... click here for more details »

...be responsible for the development, maintenance and implementation of test cases and scripts for both the GUI and back-end of real-time semantic search software. You will review feature requirements, produce test plans and carry out testing and analysis of the results on... click here for more details »