director of studies jobs in Brentford

£100 – £125 per day

You will be the subject matter expert for all GSK HR data privacy governance and controls. Specifically, you will lead strategic activities to protect all employee data across the HR function, driving robust ‘best-in-class’ governance programmes to ensure global compliance with GSK’s legislative and regulatory responsibilities.

You will be the subject matter expert for all GSK HR data privacy governance and controls. Specifically, you will lead strategic activities to protect all employee data across the HR function, driving robust ‘best-in-class’ governance programmes to ensure global compliance with GSK’s legislative and regulatory responsibilities.

Please Note: We have multiple positions available in Canada (Mississauga/Ontario), USA (Collegeville, PA), UK (Brentford, Stevenage) & Poland (Warsaw). Due to the current COVID pandemic we are open to talent working virtually from home during this time, although the long-term intent is to be located close to the mentioned hub sites. Would you like to be part of GSK's clinical development team,...

Site Name: UK - London - Brentford, Belgium-Rixensart, Belgium-Wavre, Italy - Siena, Upper Merion, USA - Maryland - Rockville, USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence Posted Date: Mar 24 2023 Global Communications and Government Affairs Director, Early-Stage Vaccines GSK has an industry-leading pipeline of vaccines and the broadest portfolio of vaccines platform...

Are you a proven Clinical Study Manager with operational credibility, demonstrated ability to input to and influence studies/projects through operational expertise, and demonstrated excellence in stakeholder management? If so, then this position could be a perfect fit for you! We are currently seeking a Clinical Global Study Delivery Lead to join the team on a permanent, full-time basis. As the...

Please Note: We have multiple positions available in Canada (Mississauga/Ontario), USA (Collegeville, PA), UK (Brentford, Stevenage) & Poland (Warsaw). Due to the current COVID pandemic we are open to talent working virtually from home during this time, although the long-term intent is to be located close to the mentioned hub sites. Would you like to be part of GSK’s clinical development team,...

Site Name: USA - Pennsylvania - Upper Providence, Canada - Ontario - Mississauga, GSK House, UK - Hertfordshire - Stevenage Posted Date: Mar 23 2023 GSK site preferred locations: Upper Providence - Collegeville, PA, Mississauga, Canada, Stevenage, UK, GSK House. New GSK UK Headquarters - move from GSK House, Brentford We're moving towards a more sustainable future with our new headquarters....

We have a great opportunity for you in the Bioanalysis, Immunogenicity and Biomarkers (BIB) department at GSK! We are looking for a bioanalytical subject matter expert (SME) to join Bioanalysis, Immunogenicity and Biomarkers hub in China. The team will support all Pharmacokinetic (PK) Bioanalysis, Immunogenicity and Biomarker data delivery endpoints using various analytical platforms (LC/MS,...

Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.

You will be responsible to perform activities for one or several projects, and you will have to ability to support most types of studies (different therapeutic areas, pivotal/critical path, Phase III, efficacy studies just to name a few).

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive.Getting ahead means preventing disease as well as treating it, and we aim to impact the health of...

You will be responsible for performing activities for one or several projects, and you will have to ability to support most types of studies (different therapeutic areas, pivotal/critical path, Phase III, efficacy studies just to name a few). Moreover, you will act as a role model in the clinical trial process, and you will coach and mentor less experienced SDSs .

The Local Study Manager (LSM) is the lead role for within-country operational feasibility, planning and delivery of Phase I-IV clinical trials and epidemiological studies in a specific country or cluster of countries. They are accountable for within-country execution and delivery of assigned studies to time, budget and quality expectations as defined in the clinical development plan and study...

GSK is seeking talented and motivated individuals for the position of Clinical Laboratory Study Manager within CLS Clinical Sample Strategy & Management Group. This role will provide YOU great opportunity to be a part of core Study Team and lead key laboratory activities. Within newly formed enthusiastic and dynamic CLSM’s medicines team YOU will have number of opportunities to grow your...

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive.Getting ahead means preventing disease as well as treating it, and we aim to impact the health of...

We’re combining the power of genetic and genomic insights into what causes disease, with the speed and scale of artificial intelligence and machine learning (AI/ML) to make better predictions about who a treatment might work for, and why. We believe this powerful combination of data and technology holds the key to fundamentally transforming medical discovery for the better, improving R&D success...

Are you a pharma Medical Director who would you be keen to join GSK's oncology clinical development organization as it continues its commitment to improve the lives of patients with multiple myeloma? If so, then this Senior Medical Director role at GSK is a must to consider. GSK ONCOLOGY Our Oncology R&D organization is building a diverse portfolio of Oncology medicines, focused on maximizing...

ViiV Healthcare is an independent, global specialist HIV company that is committed to delivering innovative new options for the care and treatment of people living with HIV/AIDS. ViiV is 100% dedicated to HIV medicines and research, and completely focused on people affected by HIV/AIDS. As part of the Research & Development and Global Medical Group (RDGM), the Global Health Outcomes (GHO) team is...

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.

Associate Director Scientific Writing Apply experience, scientific and operational expertise, and leadership in a matrix organization to provide Medical Writing strategy to one or more Therapy Area assets by driving the design and delivery of high-quality fit for purpose clinical documents including those for regulatory submissions, the plans for implementation of efficient and accelerated ways...