Katalyst CRO
Join to apply for the
Global Regulatory Strategist
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Katalyst CRO Join to apply for the
Global Regulatory Strategist
role at
Katalyst CRO Get AI-powered advice on this job and more exclusive features. Develop global or US regulatory strategy for Oncology products in development and through life cycle management, considering all relevant guidance, commercial needs, and company objectives. Develop strategic direction and provide leadership for all regulatory interactions with FDA/global regulatory authorities. Lead regulatory dossier submissions to global and/or FDA (IND, BLA, NDA, and supplements) utilizing internal and external resources; ensure appropriate quality controls in place for compliant submissions. Writing regulatory documents (e.g. new INDs, briefing book content, BT Designation request, Priority Review Requests, ODD); reviewing core documents to support IND/BLA/NDA, in conjunction with EUL or GRL as needed. Provide strategic direction (and content input) on US Labelling. Anticipate and interpret key trends and changes in the global/US regulatory environment and provide strategic guidance regarding development plans as a result. Foster positive relationships with FDA. Build and maintain a strong, collaborative relationship with all key stakeholders including Commercial, Medical Affairs, Promotion & Compliance, Global Development, and other functions key to the success of product development. Interact routinely and will develop a strong team environment with colleagues throughout GRS.
Roles & Responsibilities
Develop global or US regulatory strategy for Oncology products in development and through life cycle management, considering all relevant guidance, commercial needs, and company objectives. Develop strategic direction and provide leadership for all regulatory interactions with FDA/global regulatory authorities. Lead regulatory dossier submissions to global and/or FDA (IND, BLA, NDA, and supplements) utilizing internal and external resources; ensure appropriate quality controls in place for compliant submissions. Writing regulatory documents (e.g. new INDs, briefing book content, BT Designation request, Priority Review Requests, ODD); reviewing core documents to support IND/BLA/NDA, in conjunction with EUL or GRL as needed. Provide strategic direction (and content input) on US Labelling. Anticipate and interpret key trends and changes in the global/US regulatory environment and provide strategic guidance regarding development plans as a result. Foster positive relationships with FDA. Build and maintain a strong, collaborative relationship with all key stakeholders including Commercial, Medical Affairs, Promotion & Compliance, Global Development, and other functions key to the success of product development. Interact routinely and will develop a strong team environment with colleagues throughout GRS.
Education & Experience
Ph.D., M.D., PharmD., MS or commensurate experience. Significant experience in regulatory affairs (e.g., 3-5 years). Expert understanding of policy, laws, regulations, and guidelines as they apply to U.S. FDA for drug development and approval. Expert understanding of drug development process and understanding of scientific content and complexities related to a project in Oncology. Direct experience in developing strategy and leading teams through interactions with FDA. Extensive experience in initiating and conducting successful interactions within FDA. Strong ability to work successfully in a matrix environment and to lead teams successfully toward drug approvals. Strong team player, using both internal and external resources to execute regulatory activities and working across organizational, functional, and geographic boundaries to achieve company goals. Communicates opinions, facts and thoughts with clarity, transparency, and honesty. Demonstrates ownership of results within (and beyond) area of responsibility. Sets clear and high expectations and holds self and others accountable for decisions and results achieved. Looks for opportunities for continuous improvement. Seniority level
Seniority level Associate Employment type
Employment type Contract Job function
Job function Business Development and Sales Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x Sign in to set job alerts for “Global Strategist” roles.
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Global Regulatory Strategist
role at
Katalyst CRO Join to apply for the
Global Regulatory Strategist
role at
Katalyst CRO Get AI-powered advice on this job and more exclusive features. Develop global or US regulatory strategy for Oncology products in development and through life cycle management, considering all relevant guidance, commercial needs, and company objectives. Develop strategic direction and provide leadership for all regulatory interactions with FDA/global regulatory authorities. Lead regulatory dossier submissions to global and/or FDA (IND, BLA, NDA, and supplements) utilizing internal and external resources; ensure appropriate quality controls in place for compliant submissions. Writing regulatory documents (e.g. new INDs, briefing book content, BT Designation request, Priority Review Requests, ODD); reviewing core documents to support IND/BLA/NDA, in conjunction with EUL or GRL as needed. Provide strategic direction (and content input) on US Labelling. Anticipate and interpret key trends and changes in the global/US regulatory environment and provide strategic guidance regarding development plans as a result. Foster positive relationships with FDA. Build and maintain a strong, collaborative relationship with all key stakeholders including Commercial, Medical Affairs, Promotion & Compliance, Global Development, and other functions key to the success of product development. Interact routinely and will develop a strong team environment with colleagues throughout GRS.
Roles & Responsibilities
Develop global or US regulatory strategy for Oncology products in development and through life cycle management, considering all relevant guidance, commercial needs, and company objectives. Develop strategic direction and provide leadership for all regulatory interactions with FDA/global regulatory authorities. Lead regulatory dossier submissions to global and/or FDA (IND, BLA, NDA, and supplements) utilizing internal and external resources; ensure appropriate quality controls in place for compliant submissions. Writing regulatory documents (e.g. new INDs, briefing book content, BT Designation request, Priority Review Requests, ODD); reviewing core documents to support IND/BLA/NDA, in conjunction with EUL or GRL as needed. Provide strategic direction (and content input) on US Labelling. Anticipate and interpret key trends and changes in the global/US regulatory environment and provide strategic guidance regarding development plans as a result. Foster positive relationships with FDA. Build and maintain a strong, collaborative relationship with all key stakeholders including Commercial, Medical Affairs, Promotion & Compliance, Global Development, and other functions key to the success of product development. Interact routinely and will develop a strong team environment with colleagues throughout GRS.
Education & Experience
Ph.D., M.D., PharmD., MS or commensurate experience. Significant experience in regulatory affairs (e.g., 3-5 years). Expert understanding of policy, laws, regulations, and guidelines as they apply to U.S. FDA for drug development and approval. Expert understanding of drug development process and understanding of scientific content and complexities related to a project in Oncology. Direct experience in developing strategy and leading teams through interactions with FDA. Extensive experience in initiating and conducting successful interactions within FDA. Strong ability to work successfully in a matrix environment and to lead teams successfully toward drug approvals. Strong team player, using both internal and external resources to execute regulatory activities and working across organizational, functional, and geographic boundaries to achieve company goals. Communicates opinions, facts and thoughts with clarity, transparency, and honesty. Demonstrates ownership of results within (and beyond) area of responsibility. Sets clear and high expectations and holds self and others accountable for decisions and results achieved. Looks for opportunities for continuous improvement. Seniority level
Seniority level Associate Employment type
Employment type Contract Job function
Job function Business Development and Sales Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x Sign in to set job alerts for “Global Strategist” roles.
State Partnerships Manager (New York, NY)
New York, NY $36,000 - $185,350 1 month ago Lead, Institutional Strategy and Communications
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New York, NY $95,000.00 - $105,000.00 2 weeks ago Business Analyst with P&C Insurance - Remote
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Program & Partnerships Manager, ConnectED (hourly)
Program & Partnerships Manager, ConnectED
New York, NY $95,000.00 - $115,000.00 1 week ago Guidewire Policy Center Business Analyst with Kufri - Remote
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We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr