Johnson & Johnson Innovative Medicine
Lead Regulatory Scientist, Global Regulatory Affairs (Oncology)
Johnson & Johnson Innovative Medicine, Raritan, New Jersey, us, 08869
Overview
J Janssen Research & Development, LLC is looking to recruit a
Lead Regulatory Scientist, Global Regulatory Affairs (Oncology) . The preferred location is New Jersey or Pennsylvania. At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Key Responsibilities
Provide support to the Regional Regulatory Liaison, Regional Therapeutic Area Leader and/or Global Regulatory Leader (GRL) for regulatory activities for products in the assigned portfolio, including assuring that content and intent of regulatory filings support the global regulatory strategy Participate in global regulatory team meetings as appropriate Advise the regulatory team on applicable regulatory requirements, project specific regulatory issues as assigned Develop an understanding of the regional regulatory environment, competitor intelligence and therapeutic area Act as back-up for contact with Regulatory Agencies as needed Draft cover letters for Regulatory Agency communication Assist in the preparation of meetings with Regulatory Agencies Collaborate with Local Operating Companies (LOCs), and ensure responses to queries are made in a timely manner, and that content is consistent with the regulatory strategy Assist in the development and improvement of processes related to regulatory submissions Review clinical trial plans and protocols and ensure alignment with regulatory requirements Provide regulatory support throughout registration process and life-cycle management Advise team regarding required documents and submission strategies (in collaboration with LOCs as appropriate) Assist with timely availability of submission documents and ensure that all document components are in place on time Draft and review some document content (depending on level of regulatory knowledge/expertise) Prepare, hold and lead cross-functional team meetings as appropriate Understand submission details and collaborate closely with Submission Management Review and approve submission plans Review of submission documents to ensure compliance with regulatory requirements Assist with submission and acceptance of the submission package Ensure country-specific submission packages are made available to the LOCs in accordance with agreed plans Provide regulatory input for and appropriate follow-up to inspections, audits, litigation support and product complaints Serve as the Regulatory representative on specific multi-discipline teams Stay on top of current and pending approvals in specific therapeutic areas and knowledgeable of laws, guidances and requirements related to those areas Qualifications
Education Bachelor’s Degree plus 6 years of industry experience (required) Master level degree plus 4 years of proven experience (preferred) PharmD/PhD with 2 year relevant experience (preferred) Experience and Skills Previous health regulated industry experience Understanding of the drug development process Solid understanding of the regulatory submission and approval process Knowledge of US guidelines and practices in the regulatory environment Must be able to work optimally within a diverse team environment and as an individual contributor Project management, oral & written communication skills, organization and multi-tasking skills Teamwork skills, including effective communication and conflict resolution skills Exercises strong organizational and time management skills Demonstrated ability of critical thinking and contingency planning with respect corporate objectives Effective critical thinking including problem solving and goal setting for improved efficiencies Preferred Direct experience in regulatory affairs is desirable Oncology Drug Development experience Regulatory, Clinical or R&D experience with products in early and late development stages Experience responding to FDA requests, handling FDA interactions, and lifecycle management of IND/NDA/BLA applications Other This position may require less than 10% travel. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. The anticipated base pay range for this position is: $105,000-$169,050 Additional Description For Pay Transparency: Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for time off benefits including Vacation, Sick time, Holiday pay, Work, Personal and Family Time, Parental Leave, Condolence Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off. Additional information can be found at the link below: https://www.careers.jnj.com/employee-benefits Seniority level
Not Applicable Employment type
Full-time Job function
Legal Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Johnson & Johnson Innovative Medicine by 2x Get notified about new Regulatory Scientist jobs in Raritan, NJ.
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J Janssen Research & Development, LLC is looking to recruit a
Lead Regulatory Scientist, Global Regulatory Affairs (Oncology) . The preferred location is New Jersey or Pennsylvania. At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Key Responsibilities
Provide support to the Regional Regulatory Liaison, Regional Therapeutic Area Leader and/or Global Regulatory Leader (GRL) for regulatory activities for products in the assigned portfolio, including assuring that content and intent of regulatory filings support the global regulatory strategy Participate in global regulatory team meetings as appropriate Advise the regulatory team on applicable regulatory requirements, project specific regulatory issues as assigned Develop an understanding of the regional regulatory environment, competitor intelligence and therapeutic area Act as back-up for contact with Regulatory Agencies as needed Draft cover letters for Regulatory Agency communication Assist in the preparation of meetings with Regulatory Agencies Collaborate with Local Operating Companies (LOCs), and ensure responses to queries are made in a timely manner, and that content is consistent with the regulatory strategy Assist in the development and improvement of processes related to regulatory submissions Review clinical trial plans and protocols and ensure alignment with regulatory requirements Provide regulatory support throughout registration process and life-cycle management Advise team regarding required documents and submission strategies (in collaboration with LOCs as appropriate) Assist with timely availability of submission documents and ensure that all document components are in place on time Draft and review some document content (depending on level of regulatory knowledge/expertise) Prepare, hold and lead cross-functional team meetings as appropriate Understand submission details and collaborate closely with Submission Management Review and approve submission plans Review of submission documents to ensure compliance with regulatory requirements Assist with submission and acceptance of the submission package Ensure country-specific submission packages are made available to the LOCs in accordance with agreed plans Provide regulatory input for and appropriate follow-up to inspections, audits, litigation support and product complaints Serve as the Regulatory representative on specific multi-discipline teams Stay on top of current and pending approvals in specific therapeutic areas and knowledgeable of laws, guidances and requirements related to those areas Qualifications
Education Bachelor’s Degree plus 6 years of industry experience (required) Master level degree plus 4 years of proven experience (preferred) PharmD/PhD with 2 year relevant experience (preferred) Experience and Skills Previous health regulated industry experience Understanding of the drug development process Solid understanding of the regulatory submission and approval process Knowledge of US guidelines and practices in the regulatory environment Must be able to work optimally within a diverse team environment and as an individual contributor Project management, oral & written communication skills, organization and multi-tasking skills Teamwork skills, including effective communication and conflict resolution skills Exercises strong organizational and time management skills Demonstrated ability of critical thinking and contingency planning with respect corporate objectives Effective critical thinking including problem solving and goal setting for improved efficiencies Preferred Direct experience in regulatory affairs is desirable Oncology Drug Development experience Regulatory, Clinical or R&D experience with products in early and late development stages Experience responding to FDA requests, handling FDA interactions, and lifecycle management of IND/NDA/BLA applications Other This position may require less than 10% travel. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. The anticipated base pay range for this position is: $105,000-$169,050 Additional Description For Pay Transparency: Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for time off benefits including Vacation, Sick time, Holiday pay, Work, Personal and Family Time, Parental Leave, Condolence Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off. Additional information can be found at the link below: https://www.careers.jnj.com/employee-benefits Seniority level
Not Applicable Employment type
Full-time Job function
Legal Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Johnson & Johnson Innovative Medicine by 2x Get notified about new Regulatory Scientist jobs in Raritan, NJ.
#J-18808-Ljbffr