Current jobs related to Associate Director of Biopharmaceutical Development - Cambridge, Cambridgeshire - Flagship Pioneering, Inc.
-
Biopharmaceutical Characterisation Scientist
6 days ago
Cambridge, Cambridgeshire, United Kingdom Intertek Full timeAbout IntertekIntertek is a global leader in quality assurance and testing, and we are currently seeking a highly skilled Biopharmaceutical Characterisation Scientist to join our team in Melbourne.About the RoleWe are looking for an experienced scientist to utilise their knowledge, experience and skillset in LC-MS/MS for the analysis of primarily...
-
Biopharmaceutical Characterisation Scientist
2 weeks ago
Cambridge, Cambridgeshire, United Kingdom Intertek Full timeAbout the RoleWe are seeking a highly skilled Biopharmaceutical Characterisation Scientist to join our team at Intertek. As a key member of our laboratory, you will be responsible for utilising your expertise in LC-MS/MS to analyse biopharmaceutical products, ranging from small molecules to large biological molecules.Key ResponsibilitiesDevelop and validate...
-
Associate Director
2 weeks ago
Cambridge, Cambridgeshire, United Kingdom Amgen Full timeJob SummaryWe are seeking a highly experienced and skilled Associate Director to lead our Global Clinical Program Management team. As a key member of our organization, you will be responsible for delivering high-quality clinical trials on time and within budget, while maintaining global business relationships and communicating program status to senior...
-
Biopharmaceutical Characterisation Scientist
1 week ago
Cambridge, Cambridgeshire, United Kingdom Intertek Full timeAbout IntertekIntertek is a global leader in quality assurance and testing, with a strong presence in the biopharmaceutical industry. We are seeking a highly skilled Biopharmaceutical Characterisation Scientist to join our team in Melbourne.About the RoleThe successful candidate will be responsible for utilising their knowledge and experience in LC-MS/MS to...
-
Cambridge, Cambridgeshire, United Kingdom Intertek Full timeAbout IntertekIntertek is a global leader in quality assurance and testing. We are seeking a highly skilled Biopharmaceutical Characterisation Specialist to join our team in Melbourne.Key ResponsibilitiesDevelop and validate methods for the analysis of biopharmaceuticals using LC-MS/MS instruments.Perform routine analysis, method development, and method...
-
Biopharmaceutical Characterisation Specialist
1 month ago
Cambridge, Cambridgeshire, United Kingdom Intertek Full timeAbout the RoleWe are seeking a highly skilled Biological Characterisation Scientist to join our team at Intertek Melbourn. As a key member of our team, you will be responsible for utilising your expertise in LC-MS/MS to analyse biopharmaceutical products, ranging from small molecules to large biological molecules.Key ResponsibilitiesDevelop and validate...
-
Biopharmaceutical Characterisation Specialist
1 month ago
Cambridge, Cambridgeshire, United Kingdom Intertek Full timeAbout the RoleWe are seeking a highly skilled Biological Characterisation Scientist to join our team at Intertek Melbourn. As a key member of our team, you will be responsible for utilising your expertise in LC-MS/MS to analyse biopharmaceutical products, ranging from small molecules to large biological molecules.Key ResponsibilitiesDevelop and validate...
-
Cambridge, Cambridgeshire, United Kingdom Amgen Full timeJob SummaryWe are seeking an experienced Associate Director to lead our Global Clinical Program Management team. As a key member of our organization, you will be responsible for delivering high-quality clinical trials on time and within budget.Key ResponsibilitiesDevelop and implement global clinical program operational strategies, plans, and risk...
-
Cambridge, Cambridgeshire, United Kingdom Amgen Full timeJob SummaryWe are seeking an experienced Associate Director to lead our Global Clinical Program Management team. As a key member of our organization, you will be responsible for delivering high-quality clinical trials on time and within budget.Key ResponsibilitiesDevelop and implement global clinical program operational strategies, plans, and risk...
-
Cambridge, Cambridgeshire, United Kingdom Amgen Full timeJob SummaryWe are seeking an experienced Associate Director to lead our Global Clinical Program Management team. As a key member of our organization, you will be responsible for delivering high-quality clinical trials on time and within budget.Key ResponsibilitiesDevelop and implement global clinical program operational strategies, plans, and risk...
-
Cambridge, Cambridgeshire, United Kingdom Amgen Full timeJob SummaryWe are seeking an experienced Associate Director to lead our Global Clinical Program Management team. As a key member of our organization, you will be responsible for delivering high-quality clinical trials on time and within budget.Key ResponsibilitiesDevelop and implement global clinical program operational strategies, plans, and risk...
-
Associate Director, Asset Management
1 month ago
Cambridge, Cambridgeshire, United Kingdom Bicycle Therapeutics Full timeJob Title: Associate Director, Asset ManagementBicycle Therapeutics is a clinical-stage biopharmaceutical company that is revolutionizing the field of medicine with its innovative approach to drug development. We are seeking an experienced Associate Director, Asset Management to join our team and play a critical role in shaping our global talent acquisition...
-
Cambridge, Cambridgeshire, United Kingdom Amgen Full timeJob SummaryWe are seeking an experienced Associate Director to lead our Global Clinical Program Management team. As a key member of our organization, you will be responsible for delivering high-quality clinical trials on time and within budget.Key ResponsibilitiesDevelop and implement global clinical program operational strategies, plans, and risk...
-
Cambridge, Cambridgeshire, United Kingdom Amgen Full timeJob SummaryWe are seeking an experienced Associate Director to lead our Global Clinical Program Management team. As a key member of our organization, you will be responsible for delivering high-quality clinical trials on time and within budget.Key ResponsibilitiesDevelop and implement global clinical program operational strategies, plans, and risk...
-
Associate Director, R&D Corrective Actions
4 weeks ago
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeAbout the RoleWe are seeking an experienced Associate Director to lead our R&D Corrective Actions (CAPA) program and associated processes. The successful candidate will oversee the effectiveness and continuous improvement of the CAPA program, ensuring adherence to regulations and industry best practices.Key ResponsibilitiesLead the R&D CAPA program, ensuring...
-
Associate Director, R&D Corrective Actions
4 weeks ago
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeAbout the RoleWe are seeking an experienced Associate Director to lead our R&D Corrective Actions (CAPA) program and associated processes. The successful candidate will oversee the effectiveness and continuous improvement of the CAPA program, ensuring adherence to regulations and industry best practices.Key ResponsibilitiesLead the R&D CAPA program, ensuring...
-
Cambridge, Cambridgeshire, United Kingdom Amgen Full timeJob SummaryWe are seeking an experienced Associate Director to lead our Global Clinical Program Management team. As a key member of our organization, you will be responsible for delivering high-quality clinical trials on time and within budget.Key ResponsibilitiesDevelop and implement global clinical program operational strategies, plans, and risk...
-
Cambridge, Cambridgeshire, United Kingdom Amgen Full timeJob SummaryWe are seeking an experienced Associate Director to lead our Global Clinical Program Management team. As a key member of our organization, you will be responsible for delivering high-quality clinical trials on time and within budget.Key ResponsibilitiesDevelop and implement global clinical program operational strategies, plans, and risk...
-
Associate Director Business Analyst
3 weeks ago
Cambridge, Cambridgeshire, United Kingdom Bristol-Myers Squibb Full timeTransform Lives and Careers with Bristol-Myers SquibbJoin our team of high-achieving professionals as an Associate Director, Business Analyst in the LIMS/ELN Product Team. This pivotal role involves aligning scientific research needs with IT solutions, focusing on Laboratory Information Management Systems (LIMS) and Electronic Laboratory Notebooks (ELN).Key...
-
Associate Director Business Analyst
3 weeks ago
Cambridge, Cambridgeshire, United Kingdom Bristol-Myers Squibb Full timeTransform Lives and Careers with Bristol-Myers SquibbJoin our team of high-achieving professionals as an Associate Director, Business Analyst in the LIMS/ELN Product Team. This pivotal role involves aligning scientific research needs with IT solutions, focusing on Laboratory Information Management Systems (LIMS) and Electronic Laboratory Notebooks (ELN).Key...
Associate Director of Biopharmaceutical Development
1 month ago
At Flagship Pioneering, Inc., we're harnessing the power of scientific innovation to create novel treatment options for patients. As an Associate Director of Biopharmaceutical Development, you'll play a pivotal role in conceiving and developing life-changing treatments for serious diseases with unmet medical need.
Key Responsibilities:- Manage high-complexity projects, leveraging collaborations with Flagship platform companies to drive innovation.
- Think strategically at the asset and portfolio level, ensuring alignment with business objectives.
- Develop integrated development plans and ensure execution and tracking of critical activities for project teams.
- Collaborate closely with internal stakeholders to ensure smooth execution of partnership goals and activities.
- Analyze market data and competitor activities to identify potential opportunities and threats.
- Provide strategic insights and recommendations to senior management regarding potential partnership initiatives and market expansion strategies.
- PhD, Master's, or BS/BA/MBA degree in a relevant field.
- 8+ years' experience in drug discovery development or scientific, functional experience.
- 6+ years' drug development project management experience.
- Scientific/research background, preferably with experience in Metabolic, Immunology, CV, and/or renal disease area(s).
- Strong understanding of the biopharmaceutical landscape, including key players, emerging trends, and technological advancements.
- Demonstrated ability to work effectively with cross-functional teams and manage multiple projects simultaneously.
