Current jobs related to Prologue Medicines, Inc. - Cambridge, Cambridgeshire - Flagship Pioneering
-
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeSenior Director, Quantitative PharmacologyRegeneron Pharmaceuticals, Inc is seeking a highly experienced Senior Director to lead our Quantitative Pharmacology team. As a key member of our Pharmacometrics group, you will be responsible for managing PMx support for multiple programs across various therapeutic areas.Key Responsibilities:Develop and implement...
-
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeSenior Director, Quantitative PharmacologyRegeneron Pharmaceuticals, Inc is seeking a highly experienced Senior Director to lead our Quantitative Pharmacology team. As a key member of our Pharmacometrics group, you will be responsible for managing PMx support for multiple programs across various therapeutic areas.Key Responsibilities:Develop and implement...
-
Senior Quality Control Specialist
3 weeks ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob SummaryWe are seeking a highly skilled and experienced Senior Quality Control Specialist to join our Quality Control team at Regeneron Pharmaceuticals, Inc. as a part of our new Regeneron Cell Medicines group. The successful candidate will be responsible for overseeing contract lab testing and supporting safety testing for novel drug products targeting...
-
Senior Quality Control Specialist
3 weeks ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob SummaryWe are seeking a highly skilled and experienced Senior Quality Control Specialist to join our Quality Control team at Regeneron Pharmaceuticals, Inc. as a part of our new Regeneron Cell Medicines group. The successful candidate will be responsible for overseeing contract lab testing and supporting safety testing for novel drug products targeting...
-
Senior Director of Quantitative Pharmacology
7 days ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob SummaryAs a Senior Director in Pharmacometrics, this individual will be responsible for managing PMx support for a number of programs in one or more therapeutic focus areas of the development portfolio. In this capacity, the Senior Director is accountable for the successful and timely completion of all assignments encompassing a broad array of...
-
Senior Director of Quantitative Pharmacology
7 days ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob SummaryAs a Senior Director in Pharmacometrics, this individual will be responsible for managing PMx support for a number of programs in one or more therapeutic focus areas of the development portfolio. In this capacity, the Senior Director is accountable for the successful and timely completion of all assignments encompassing a broad array of...
-
Senior Director of Quantitative Pharmacology
4 days ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob SummaryAs a Senior Director in Pharmacometrics, you will be responsible for managing PMx support for a number of programs in one or more therapeutic focus areas of the development portfolio. In this capacity, you will be accountable for the successful and timely completion of all assignments encompassing a broad array of deliverables in support of the...
-
Senior Director of Quantitative Pharmacology
4 days ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob SummaryAs a Senior Director in Pharmacometrics, you will be responsible for managing PMx support for a number of programs in one or more therapeutic focus areas of the development portfolio. In this capacity, you will be accountable for the successful and timely completion of all assignments encompassing a broad array of deliverables in support of the...
-
Lead LIMS Developer
19 hours ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob Title: Lead LIMS DeveloperWe are seeking a highly skilled Lead LIMS Developer to join our team at Regeneron Pharmaceuticals, Inc. in Cambridge, MA. As a key member of our Regeneron Cell Medicines (RCM) unit, you will play a critical role in supporting our scientists and engineers in the development of novel cell therapies.Key Responsibilities:Interface...
-
Lead LIMS Developer
7 days ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob Title: Lead LIMS DeveloperWe are seeking a highly skilled Lead LIMS Developer to join our team at Regeneron Pharmaceuticals, Inc. in Cambridge, MA. As a key member of our Regeneron Cell Medicines (RCM) unit, you will play a critical role in supporting our scientists and engineers in the development of novel cell therapies.Key Responsibilities:Interface...
-
Lead LIMS Developer
7 days ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob Title: Lead LIMS DeveloperWe are seeking a highly skilled Lead LIMS Developer to join our team at Regeneron Pharmaceuticals, Inc. in Cambridge, MA. As a key member of our Regeneron Cell Medicines (RCM) unit, you will play a critical role in supporting our scientists and engineers in the development of novel cell therapies.Key Responsibilities:Interface...
-
Lead LIMS Developer
22 hours ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob Title: Lead LIMS DeveloperWe are seeking a highly skilled Lead LIMS Developer to join our team at Regeneron Pharmaceuticals, Inc. in Cambridge, MA. As a key member of our Regeneron Cell Medicines (RCM) unit, you will play a critical role in supporting our scientists and engineers in the development of novel cell therapies.Key Responsibilities:Interface...
-
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences, Inc. Full timeJob Title: Global Regulatory Affairs Business Operations DirectorJob Summary:We are seeking a highly experienced and skilled Global Regulatory Affairs Business Operations Director to join our team at Gilead Sciences, Inc. This role will be responsible for leading the development and implementation of global regulatory affairs business operations strategies,...
-
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences, Inc. Full timeJob Title: Global Regulatory Affairs Business Operations DirectorJob Summary:We are seeking a highly experienced and skilled Global Regulatory Affairs Business Operations Director to join our team at Gilead Sciences, Inc. This role will be responsible for leading the development and implementation of global regulatory affairs business operations strategies,...
-
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences, Inc. Full timeJob Title: Global Regulatory Affairs Business Operations DirectorJob Summary:We are seeking a highly experienced and skilled Global Regulatory Affairs Business Operations Director to join our team at Gilead Sciences, Inc. This role will be responsible for leading the development and implementation of global regulatory affairs business operations strategies,...
-
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences, Inc. Full timeJob Title: Global Regulatory Affairs Business Operations DirectorJob Summary:We are seeking a highly experienced and skilled Global Regulatory Affairs Business Operations Director to join our team at Gilead Sciences, Inc. This role will be responsible for leading the development and implementation of global regulatory affairs business operations strategies,...
-
Senior LIMS Developer
4 days ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals Inc. Full timeJob Title: Senior LIMS DeveloperWe are seeking a highly skilled Senior LIMS Developer to join our team at Regeneron Pharmaceuticals Inc. in Cambridge, MA. As a key member of our Regeneron Cell Medicines (RCM) unit, you will play a critical role in supporting our scientists and engineers in the design, development, and implementation of Laboratory Information...
-
Senior LIMS Developer
4 days ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals Inc. Full timeJob Title: Senior LIMS DeveloperWe are seeking a highly skilled Senior LIMS Developer to join our team at Regeneron Pharmaceuticals Inc. in Cambridge, MA. As a key member of our Regeneron Cell Medicines (RCM) unit, you will play a critical role in supporting our scientists and engineers in the design, development, and implementation of Laboratory Information...
-
Regulatory Compliance Specialist
3 weeks ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob SummaryWe are seeking a highly skilled and experienced Senior Quality Control Specialist to join our Quality Control team at Regeneron Pharmaceuticals, Inc. as a part of our new Regeneron Cell Medicines group.Key ResponsibilitiesOversee contract lab testing and support safety testing for novel drug products targeting oncological indications.Provide...
-
Regulatory Compliance Specialist
3 weeks ago
Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full timeJob SummaryWe are seeking a highly skilled and experienced Senior Quality Control Specialist to join our Quality Control team at Regeneron Pharmaceuticals, Inc. as a part of our new Regeneron Cell Medicines group.Key ResponsibilitiesOversee contract lab testing and support safety testing for novel drug products targeting oncological indications.Provide...
Prologue Medicines, Inc.
3 months ago
Cambridge, MA USA
Prologue Medicines, Inc. is a privately held early-stage company investigating secreted protein function and regulation in human physiology by combining a newly developed high throughput -omics platform with cutting edge cellular biology approaches and machine learning. Our mission is to leverage natural evolution to understand drivers and early biomarkers in the secretome which underlie chronic disease and develop next generation of therapeutics with increased potency & specificity.
One of Prologue's founding principles is to build an inclusive and exciting working environment that fosters personal and professional growth by ensuring that all team members contribute to and feel ownership of our scientific vision.
Flagship Pioneering is a biotechnology company that invents and builds platform companies, each with the potential for multiple products that transform human health or sustainability. Since its launch in 2000, Flagship has originated and fostered more than 100 scientific ventures, resulting in more than $90 billion in aggregate value. Many of the companies Flagship has founded have addressed humanity's most urgent challenges: vaccinating billions of people against COVID-19, curing intractable diseases, improving human health, preempting illness, and feeding the world by improving the resiliency and sustainability of agriculture.
Flagship has been recognized twice on FORTUNE's "Change the World" list, an annual ranking of companies that have made a positive social and environmental impact through activities that are part of their core business strategies, and has been twice named to Fast Company's annual list of the World's Most Innovative Companies. Learn more about Flagship at .
Position Summary:
Prologue Medicines, Inc. seeks a highly motivated and creative Sr./Director of Strategy & Operations to join our team.
- This role will partner across all functions to drive collaboration, cross-functional clarity, alignment, and successful implementation on key projects, initiatives, and operations that are critical to Prologue.
- Responsibilities include involvement in R&D and corporate operations, program management, due diligence on new platform opportunities, indication expansion efforts and portfolio strategy optimization.
- The role also involves crafting and driving strategic decision making and planning at an organization level.
- The successful candidate will work closely with the Prologue leadership and report directly to the President.
- The role contributes to the company's success through strategic expertise and management of operational activities, thereby facilitating Prologue's growth and impact.
- Ideal candidate traits include independence, open-mindedness, goal-orientation, and excellent communication skills.
- Comfort in a fast-paced, entrepreneurial setting is a must.
Candidate Qualifications:
- PhD in Life Sciences or MBA with extensive biotechnology experience is strongly .
- 10-15 years of experience in R&D operations, research program management and planning, and/or strategy roles within the biotechnology or pharmaceutical industry.
- Strong scientific background with a deep understanding of drug discovery and development.
- Proven track record of developing and executing strategic plans in a fast-paced, high-growth environment.
- Experience in portfolio management, including assessment of platform opportunity space and identification of expansion pools, and experience in project management planning, prioritization, and execution.
- Demonstrated ability to collaborate with diverse, cross-functional teams and influence stakeholders at all levels of the organization.
- Experience in establishing and managing external relationships across all levels of the organization.
- Excellent communication and presentation skills, with the ability to effectively convey complex scientific concepts to both technical and non-technical audiences clearly and concisely.
- Highly organized and detail-oriented, with the ability to manage multiple projects and priorities simultaneously.
- Strong analytical and problem-solving skills, with the ability to think strategically and identify creative solutions to complex challenges.
- Experience working in a startup or early-stage company is highly desirable.
- Passion for driving innovation and making a positive impact on human health and sustainability.
Key Responsibilities:
- Work with the leadership team to lead and ensure flawless operation of activities across Research and Development, including driving and refining key processes and governance structures within R&D as we grow the team.
- Lead regularly scheduled operational, strategy and program updates/reviews with the executive team; manage schedule, agenda, and content for Leadership Team,All Hands, and advisory board meetings and leading discussions to ensure team-based discussions on innovation as well as drive decisions
- Prepare strategic communications utilizing a clear understanding of the business strategy and issues; develop and maintain consistent, relevant content for use in executive level communications and to support/lead projects to further organizational and business goals
- Structure complex and ambiguous problems, synthesize findings, develop creative solutions, make logically supported recommendations, and facilitate decision-making sessions
- Lead program management to track progress on goals, ensure timely delivery of key milestones, refining strategy as needed.
- Guide the portfolio management strategy to assess platform performance and identify future opportunities
- Develop market opportunity assessments and report on the competitive landscape and its impact on the company
- Support lab operations from establishing additional contracts to managing our move across facilities as well as leading space planning activities.
- Collaborate with the leadership team to drive the annual and long-term budgeting process and support fundraising activities.
- Advance partnering framework to develop and maintain map of potential partners including rationale, possible scope, comparable deals
- Lead External Alliances, establishing and maintaining relationships with collaborators and CROs.
- Coordinate with corporate & business development counsel to establish, review and maintain external contracts such as CDAs, MTAs, licenses, consulting agreements, sponsored research agreements, etc. to enable R&D and corporate operations
- Support the development and execution of the IP strategy
At Flagship, we recognize there is no perfect candidate. If you have some of the experience listed above but not all, please apply anyway. Experience comes in many forms, skills are transferable, and passion goes a long way. We are dedicated to building diverse and inclusive teams and look forward to learning more about your unique background.
Recruitment & Staffing Agencies: Flagship Pioneering and its affiliated Flagship Lab companies (collectively, "FSP") do not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to FSP or its employees is strictly prohibited unless contacted directly by Flagship Pioneering's internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of FSP, and FSP will not owe any referral or other fees with respect thereto.
Will you now or in the future require sponsorship for employment visa status (e.g., H-1B visa status)? *
If you'll require the company to commence ("sponsor") an immigration or work permit case in order to employ you, either now or at some point in the future, then you should select Yes. Otherwise, select No.
-- Do you currently reside within the continental United States? *
--
Are you able to work in the specified job location, and are you willing to relocate for this position? *
--
When are you able to start a new position? *
Do you have 5+ years of experience in Biotech? *
--
