Current jobs related to Associate Director, Regulatory Affairs - Cambridge - Marengo Therapeutics, Inc.
-
Associate Director, Regulatory Affairs
4 months ago
Cambridge, United States Bicycle Therapeutics Full timeJob DescriptionJob DescriptionCompany DescriptionBicycle Therapeutics is a clinical-stage biopharmaceutical company developing a novel class of medicines, referred to as Bicycle® molecules, for diseases that are underserved by existing therapeutics. Bicycle molecules are fully synthetic short peptides constrained with small molecule scaffolds to form two...
-
Director, Regulatory Affairs CMC
7 days ago
Cambridge, Massachusetts, United States Takeda Full timeRegulatory Affairs Director, Small MoleculesTakeda is seeking a highly experienced Regulatory Affairs Director, Small Molecules to lead our Global Regulatory Affairs CMC team. As a key member of our team, you will be responsible for overseeing the development and execution of regulatory CMC development and registration strategies.Key Responsibilities:Plan,...
-
Senior Director of Regulatory Affairs
3 days ago
Cambridge, Massachusetts, United States Apnimed Full timeJob Title: Senior Director, Regulatory AffairsApnimed is a clinical-stage pharmaceutical company dedicated to transforming the treatment of sleep apnea. We are seeking a highly experienced Senior Director of Regulatory Affairs to play a key role in advancing our innovative programs through clinical trials and commercialization globally.Key...
-
Senior Director of Regulatory Affairs
1 week ago
Cambridge, Massachusetts, United States Apnimed Full time{"title": "Senior Director of Regulatory Affairs", "content": "Job SummaryApnimed is seeking a highly experienced Senior Director of Regulatory Affairs to lead the development and execution of regulatory strategies to support the approval and commercialization of our therapies globally.This is a key role in advancing our innovative programs through clinical...
-
Director of Regulatory Affairs and Quality
2 weeks ago
Cambridge, Massachusetts, United States Philips Full timeJob SummaryWe are seeking a highly experienced and skilled Director of Regulatory Affairs and Quality to lead our Regulatory Affairs and Quality teams in the development and execution of compliant regulatory strategies and quality team/QMS responsibilities.Key ResponsibilitiesRegulatory Affairs Strategy and ExecutionDevelop and execute end-to-end regulatory...
-
Senior Director, Regulatory Affairs
2 weeks ago
cambridge, United States Apnimed Full timeApnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...
-
Senior Director, Regulatory Affairs
3 weeks ago
cambridge, United States Apnimed Full timeApnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...
-
Senior Director, Regulatory Affairs
3 weeks ago
Cambridge, United States Apnimed Full timeApnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...
-
Senior Director, Regulatory Affairs
3 weeks ago
Cambridge, United States Apnimed Full timeApnimed is a well-funded, clinical-stage pharmaceutical company working to transform the treatment of sleep apnea based on a simple idea – patients with obstructive sleep apnea could benefit from treatment with a safe and effective oral medication dosed once daily at bedtime. Our lead development program targets the neurologic control of upper airway...
-
Director of Regulatory Affairs
3 weeks ago
Cambridge, Massachusetts, United States Sarepta Therapeutics Full timeJob SummarySarepta Therapeutics is seeking a highly experienced Regulatory Strategy Director to lead our regulatory affairs efforts. As a key member of our team, you will be responsible for developing and implementing regulatory strategies that ensure compliance with global regulations and facilitate the approval of our therapeutic programs.Key...
-
Cambridge, Massachusetts, United States Apnimed Full timeAbout the RoleWe are seeking a highly experienced Senior Director to lead our Regulatory Affairs and Compliance team at Apnimed. As a key member of our leadership team, you will play a critical role in advancing our innovative sleep apnea treatments through clinical trials and commercialization globally.Key ResponsibilitiesRegulatory Strategy and Planning:...
-
Director of Regulatory Affairs
2 months ago
Cambridge, United States The Steely Group Full timeThis role serves as a Health Authority liaison and Regulatory Project Leader for multiple projects in various stages of development. More specifically, the Director, Regulatory Affairs serves as a strategic regulatory leader for assigned drug development programs and uses extensive knowledge to advise project teams on regulatory requirements to drive...
-
Director of Regulatory Affairs
2 months ago
Cambridge, United States The Steely Group Full timeThis role serves as a Health Authority liaison and Regulatory Project Leader for multiple projects in various stages of development. More specifically, the Director, Regulatory Affairs serves as a strategic regulatory leader for assigned drug development programs and uses extensive knowledge to advise project teams on regulatory requirements to drive...
-
Cambridge, Massachusetts, United States Apnimed Full timeJob SummaryWe are seeking a highly experienced Senior Director to lead our Regulatory Affairs and Compliance team at Apnimed. As a key member of our leadership team, you will be responsible for developing and executing regulatory strategies to support the approval and commercialization of our therapies globally.Key ResponsibilitiesRegulatory Strategy and...
-
Director, Global Regulatory Affairs
2 weeks ago
Cambridge, Massachusetts, United States GlaxoSmithKline Full timeAbout the RoleWe are seeking a highly skilled and experienced Regulatory Affairs Director to join our team at GlaxoSmithKline. As a key member of our Global Regulatory Affairs team, you will play a critical role in shaping our regulatory strategy and ensuring compliance with regulatory requirements.Key ResponsibilitiesDevelop and implement regulatory...
-
Senior Director, Regulatory Affairs
1 week ago
Cambridge, Massachusetts, United States Proclinical Staffing Full timeJob Summary:Proclinical Staffing is seeking a Senior Director, Regulatory Strategy to lead the development and execution of regulatory plans for programs within the assigned franchise. As an expert in regulatory affairs, you will be responsible for articulating clear and compelling regulatory strategy, highlighting risks and opportunities, and accounting for...
-
Associate Director, Regulatory CMC
4 months ago
Cambridge, United States Intellia Therapeutics Full timeWhy Join Intellia?Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases.Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to...
-
Global Head of Regulatory Affairs
4 weeks ago
Cambridge, Massachusetts, United States Takeda Full timeWe invite you to become a part of our esteemed pharmaceutical organization as a Senior Director of Global Regulatory Affairs for Pharmaceuticals. In this pivotal role, you will be instrumental in formulating and executing comprehensive regulatory strategies for pharmaceutical products throughout their lifecycle, from development to market launch. Your...
-
Cambridge, Massachusetts, United States Moderna Therapeutics Full timeAbout the RoleThe Senior Manager of Medical Writing and Regulatory Affairs is a critical position within our Clinical Development team at Moderna Therapeutics. Reporting directly to the Associate Director, Director of Medical Writing, or Senior Director of Medical Writing, this individual will play a pivotal role in delivering high-quality clinical and...
-
Regulatory Affairs Executive
4 weeks ago
Cambridge, Massachusetts, United States The Steely Group Full timeThe Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and leads regulatory projects across various development phases. This position demands a strategic regulatory leader who can effectively guide drug development initiatives by leveraging extensive expertise in regulatory frameworks.Key...
Associate Director, Regulatory Affairs
3 months ago
Job Type
Full-time
Description
Marengo Therapeutics, Inc., a clinical-stage biotech company, develops novel TCR-targeting antibodies that selectively modulate common and disease-specific T cell subsets of the germline TCR repertoire to provide lifelong protection against cancer and other diseases. With a passionate team of dedicated scientists experienced in immunology and oncology, Marengo's proprietary Selective T Cell Activation Repertoire (STAR) platform leverages an extensive biological understanding of T cell function and receptor signaling to create a world in which everyone's immune system can defeat cancer. To learn more, visit marengotx.com.
About STAR0602
STAR0602 is Marengo's lead program, the first selective T cell activator generated from Marengo's STAR platform, a library of antibodies targeting non-clonal variable (V) regions of the TCR fused to different co-stimulatory moieties. STAR0602 selectively targets a common Vb T cell subset present in all cancers and, by combining a novel non-clonal mode of TCR activation with a T cell co-stimulator in the same molecule, promotes expansion of a new population of clonally enriched, effector memory Vb T cells that turbo-charge immune system and promote a durable anti-tumor immune response. STAR0602 has undergone extensive preclinical testing, which demonstrates potent anti-tumor activity in both mouse and human ex vivo tumor models attributed to a distinct mechanism of action from existing cancer immunotherapies.
Role: Associate Director, Regulatory Affairs
Purpose of the role:
Reporting to the Chief Development Officer, this team member will play a key role in Marengo's regulatory organization/team. The Associate Director of Regulatory Affairs will oversee daily regulatory affairs activities, including the areas of clinical research, CMC, regulatory operations, nonclinical study requirements, and regulatory compliance to support the successful development, approval, and marketing of Marengo products. The ideal candidate for this role is an experienced, natural self-starter with strong organizational skills who thrives in a busy, fast-paced environment and can communicate effectively with all levels of our organization and our external partners and customers.
Who are we looking for?
•You are an energetic and passionate regulatory professional who likes to think outside of the box, challenge the norm, and is passionate about the company's mission of discovering and developing new medications
•You are a resourceful self-starter and team player with a strong result orientation
•You consider yourself as well versed
in all the corporate REGULATORY AFFAIRS
in a clinical-stage organization
•You can develop trusting relationships to gain support and achieve results at all levels of the organization
What are we looking for?
•A driven professional who knows how to work and contribute to an ever-changing working environment
•A collegial individual who enjoys working in close collaboration with leaders in the research, development, quality, clinical, and administrative areas of the company
•A willingness to learn new things, adapt to new ways, and go with the flow
•A person who thrives in a small company atmosphere
•Ability to determine task priority and maintain established deadlines
What are we offering?
• Reporting to a Regulatory Guru, who has an extensive track of accomplishments
•Membership within a growing, CARING, and collegial organization
•Being part of a passionate, involved, and cutting-edge Development Team
•Exposure to pioneering science and the discovery of drugs to help treat patients with cancer
Requirements
IF YOU ARE INTERESTED IN APPLYING, PLEASE READ ENTIRE POSTING
Responsibilities:
•Work closely with Marengo's Development & Clinical Teams to execute regulatory objectives that result in the successful entry of Marengo's assets to the clinic, their development, marketing approvals, and post-approval commercialization.
•Manage (Project Management) the preparation and timely submission of regulatory documentation to support global investigational and marketing application packages.
•Accompany our CDMO in meetings with regulatory agencies/authorities; lead the preparation of meeting documents (e.g., requests, meeting packages); virtual meetings, and other communications (e.g., Marengo's responses to information requests) with FDA and other regulatory agencies/authorities.
•Provide execution in preparation for regulatory interactions and negotiation with global regulatory agencies/authorities to resolve key regulatory issues critical to the successful development of Marengo's portfolio.
•Maintain the expertise with the most updated knowledge on regulations and regulatory guidance documents from global regulatory agencies/authorities such as FDA, EMA, and ICH; make high-quality regulatory recommendations to Marengo's senior leadership and cross-functional teams; and ensure adherence to these regulatory guidance and regulations as well as Marengo's internal procedures.
•Manage external regulatory vendors/consultants as needed.
Education and Experience:
Bachelor's degree in life sciences discipline (Biology, Chemistry, Engineering), MS/PhD/MD/PharmD preferred.
More than 8 years of biotechnology or pharmaceutical industry experience
, preferably at least 5 years of immuno-oncology experience.
Knowledge and understanding of drugs/
biologics development process
, regulatory requirements, regulations, and regulatory guidance.
Regulatory experience with INDs/CTAs, NDAs/BLAs/MAAs, and product lifecycle management.
Demonstrated skills and experience in interactions with regulatory authorities.
Excellent writing, interpersonal communications, organizational, and presentation skills. Demonstrated experience with budgeting and planning.
The candidate should be capable of operating with a high level of autonomy and will be responsible for the operational details and execution. This is a "hands-on" role. We are looking for a "do-er"
Competencies:
Adaptability : Responds resourcefully, flexibly, and positively when faced with new challenges, transitions, and demands. Willingly and effectively deals with the stress and complexities of various situations. Moves forward productively and optimistically under conditions of change and uncertainty.
Collaboration : Embodies and promotes collaboration and works effectively with others across the organization to achieve goals. Demonstrates proficient cross-company communication, cultural sensitivity, and partnership in interactions with others. Involves others in decisions and plans and credits them for their contributions and accomplishments.
Execution : Drives execution of strategic and operating plans while maintaining operational effectiveness. Conveys a strong sense of urgency around continuous improvement, achieving high-quality results, and accelerating business performance. Addresses problems directly and drives changes necessary to achieve business objectives.
Relationship Building : Establishes and maintains strong relationships internally and externally. Respects and relates well to management, colleagues, peers, and direct reports. Champions a culture of respect, diversity, and inclusion that values and respects individuals. Earns the respect of others through principled leadership, sound business ethics, and authenticity.
Location: Cambridge, MA (We are located in Lower Cambridge)
When You Join Marengo, You Will Have:
•Free parking, Cambridge location reachable by public transportation (Red Line)
•Customized and competitive health coverage, including medical offered through BCBS (PPO), dental, and vision
•Flexible Spending Accounts for medical and dependent care expenses
•Eligible from the first day for 401K, no matching
•A robust package of Marengo-paid insurance coverage, including life insurance, short-term and long-term disability
•20 days of vacation and one personal day per year, in addition to 13 company holidays
TO ALL AGENCIES: Please, no phone calls or emails to any employee of Marengo about our openings. All resumes submitted by search firms/employment agencies to any employee at Marengo via email, the internet or in any form and/or method will be deemed the sole property of Marengo unless such search firms/employment agencies were engaged by Marengo for this position and a valid agreement with Marengo is in place. In the event a candidate who was submitted outside of the Marengo agency engagement process is hired, no fee or payment of any kind will be paid.
Marengo Therapeutics, Inc. is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.
#J-18808-Ljbffr
