biochemistry studies scientist jobs in Brentford

As Safety, Evaluation and Risk Management (SERM) Principal Scientist, you will work with the SERM physician to actively manage and evaluate risks associated with assigned vaccine projects, and make recommendations for the management and communication of risks in accordance with global legal and regulatory frameworks. This may involve the following: Coordinate and perform initial analyses of...

£100 – £125 per day

You will have the opportunity to work across post-marketing products and activities too, conducting routine pharmacovigilance activities such as signal detection/evaluation, authoring key regulatory documents, managing regulatory requests and more.

You will also be resilient and calm under pressure, with strong interpersonal skills, and a continuous improvement mindset.

Site Name: UK - London - Brentford, Belgium-Wavre, Italy - Siena, Italy - VeronaPosted Date: Jan 31 2023342141 Regulatory Global Submission Manager / Project ManagerThis is an excellent opportunity for either an established Project Manager in the Life Sciences industry or Regulatory Affairs professional looking to join a truly global team/role working across multiple therapy areas.The job holder...

You will spend most of your week working in our quality labs, rotating through different departments, receiving tailored on-the-job training from our in-house industry experts. Over the 3- 4 years of the apprenticeship you will have a personal training program to help you develop and progress.

You will be studying towards a Data Science degree. If you successfully complete your apprenticeship and demonstrate the qualities we are looking for, you may be offered the opportunity to go on to further education and/or employment.

You will gain skills in data management, machine learning and statistics, whilst also developing your commercial business acumen.

You will learn how to:

You will be studying towards a MSc Medical Statistics degree from Strathclyde University .

You will be supporting the research, development, or manufacturing, and associated processes, required to bring a physical medicinal product to market.

You will coordinate and utilize specialist knowledge with brand aligned colleagues in formulating and implementing short- and long-term medical strategy to create optimal benefit for patients. Your Responsibilities

Are you energized by the opportunity to partner with key leaders in global medical science to accelerate business performance across and drive global operational support? If so, this Clinical Development Director opportunity could be an ideal opportunity to explore. Clinical Development Director, Respiratory Here at GSK, we place the patient at the heart of everything we do and as leaders in...

£100 – £125 per day

You will have the opportunity to work across post-marketing products and activities too, conducting routine pharmacovigilance activities such as signal detection/evaluation, authoring key regulatory documents, managing regulatory requests and more.

You will also be resilient and calm under pressure, with strong interpersonal skills, and a continuous improvement mindset.

You will ensure that adverse event and other safety information is efficiently evaluated in order to meet global compliance and regulatory requirements, identify the need for product labelling updates and drive proactive implementation of risk management initiatives.