Tbwa Chiat/Day Inc
Director Regulatory Affairs Strategy
Tbwa Chiat/Day Inc, Oklahoma City, Oklahoma, United States,
Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka’s mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. We have raised nearly $500M since inception in February 2024 from top-tier investors and our first program is expected to be in the clinic in the first quarter of 2025. For more information, visit www.orukatx.com.
As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture.
Job Title: Director Regulatory Affairs Strategy
Location:
Remote OR Menlo Park, CA OR Waltham, MA Position Overview:
The Director Regulatory Affairs Strategy provides global regulatory oversight and project leadership of assigned development products and reports to the Vice President Regulatory Affairs. The incumbent will be responsible for contributing to and implementing regulatory strategies and plans to expedite global product development, managing regulatory communications/interactions with health authorities, and ensuring compliance with applicable regional regulations. This position will interface closely with the cross-functional Development team, as well as with external consultants and advisors, to ensure regulatory plans and strategies are well integrated and supportive of overall corporate objectives. Key Responsibilities:
Strategic Planning Represent the Regulatory Affairs department on multidisciplinary product development teams. Develop and implement global regulatory strategy to support expedited product development for one or more programs. Contribute to content and lead preparation of global product development plans, target product profiles, orphan drug designation applications, pediatric study plans, as applicable. Research regulatory precedent and current/emerging trends related to product class and therapeutic area(s) to identify risks and opportunities for development/registration. Regulatory Operations Manage global regulatory lifecycle of assigned investigational products, including maintaining project timelines, organizing submission content, and coordinating the internal/external authoring and review of components of original investigational drug applications, amendments, and safety and annual reports. Interface with external Regulatory Operations group in the compilation and e-submission of regulatory documents. Serve as primary liaison for communication with regulatory health authority on assigned programs. Prepare team for and lead the conduct of milestone development meetings with regulatory health authority. Compliance Review and communicate current and emerging regulatory requirements for quality, preclinical, and clinical programs to ensure compliance of all development activities with applicable US and international regulations and guidelines. Participate in the development and review of standard operating procedures (SOPs); ensure SOPs are in compliance with current regulatory requirements. Assist in the archival and maintenance of regulatory application submissions and correspondence. Monitor company progress toward fulfillment of regulatory commitments. Qualifications:
Education Bachelor’s degree in a life sciences discipline; advanced degree preferred; Regulatory Affairs Certification a plus. Experience Minimum 8 years progressive pharmaceutical Regulatory Affairs experience with focus in development of drugs/biologics. Direct experience in preparation, submission and lifecycle management of global investigational/marketing applications in eCTD format, including as primary Regulatory author. Experience negotiating and directly interfacing with US and international regulatory authorities. Product development in therapeutic areas of dermatology, immunology or inflammation a plus. Skills In depth knowledge of GXP/ICH guidelines and global regulations and systems. Ability to interpret and apply complex and evolving regulatory guidance. Strong written and verbal communication, analytical, organizational and interpersonal skills. Excellent strategic planning and cross-functional project management skills. Ability to work in a dynamic environment with a high degree of flexibility. Compensation:
An appropriate financial package will be developed for the successful candidate to include a competitive base salary and equity, with a performance-related bonus opportunity. The anticipated salary range for candidates, who will work remotely or Waltham, MA or Menlo Park, CA is $200,000-225,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Oruka is a multi-state employer and this salary range may not reflect positions that work in other states. Job Location:
Position may be remote with the expectation to go on site in Menlo Park, CA OR Waltham, MA as needed OR on site in one of those locations where you will be required to be in-office 3 days/week. We're looking forward to hearing how you can contribute to our team and mission. Join us in shaping the future of our company and making a real impact every day. What We Offer:
A chance to be part of a vibrant small-company culture where your work can directly impact bringing new medicines to patients. Competitive salary and benefits package. Opportunities for professional growth and development. Apply for this job #J-18808-Ljbffr
Location:
Remote OR Menlo Park, CA OR Waltham, MA Position Overview:
The Director Regulatory Affairs Strategy provides global regulatory oversight and project leadership of assigned development products and reports to the Vice President Regulatory Affairs. The incumbent will be responsible for contributing to and implementing regulatory strategies and plans to expedite global product development, managing regulatory communications/interactions with health authorities, and ensuring compliance with applicable regional regulations. This position will interface closely with the cross-functional Development team, as well as with external consultants and advisors, to ensure regulatory plans and strategies are well integrated and supportive of overall corporate objectives. Key Responsibilities:
Strategic Planning Represent the Regulatory Affairs department on multidisciplinary product development teams. Develop and implement global regulatory strategy to support expedited product development for one or more programs. Contribute to content and lead preparation of global product development plans, target product profiles, orphan drug designation applications, pediatric study plans, as applicable. Research regulatory precedent and current/emerging trends related to product class and therapeutic area(s) to identify risks and opportunities for development/registration. Regulatory Operations Manage global regulatory lifecycle of assigned investigational products, including maintaining project timelines, organizing submission content, and coordinating the internal/external authoring and review of components of original investigational drug applications, amendments, and safety and annual reports. Interface with external Regulatory Operations group in the compilation and e-submission of regulatory documents. Serve as primary liaison for communication with regulatory health authority on assigned programs. Prepare team for and lead the conduct of milestone development meetings with regulatory health authority. Compliance Review and communicate current and emerging regulatory requirements for quality, preclinical, and clinical programs to ensure compliance of all development activities with applicable US and international regulations and guidelines. Participate in the development and review of standard operating procedures (SOPs); ensure SOPs are in compliance with current regulatory requirements. Assist in the archival and maintenance of regulatory application submissions and correspondence. Monitor company progress toward fulfillment of regulatory commitments. Qualifications:
Education Bachelor’s degree in a life sciences discipline; advanced degree preferred; Regulatory Affairs Certification a plus. Experience Minimum 8 years progressive pharmaceutical Regulatory Affairs experience with focus in development of drugs/biologics. Direct experience in preparation, submission and lifecycle management of global investigational/marketing applications in eCTD format, including as primary Regulatory author. Experience negotiating and directly interfacing with US and international regulatory authorities. Product development in therapeutic areas of dermatology, immunology or inflammation a plus. Skills In depth knowledge of GXP/ICH guidelines and global regulations and systems. Ability to interpret and apply complex and evolving regulatory guidance. Strong written and verbal communication, analytical, organizational and interpersonal skills. Excellent strategic planning and cross-functional project management skills. Ability to work in a dynamic environment with a high degree of flexibility. Compensation:
An appropriate financial package will be developed for the successful candidate to include a competitive base salary and equity, with a performance-related bonus opportunity. The anticipated salary range for candidates, who will work remotely or Waltham, MA or Menlo Park, CA is $200,000-225,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Oruka is a multi-state employer and this salary range may not reflect positions that work in other states. Job Location:
Position may be remote with the expectation to go on site in Menlo Park, CA OR Waltham, MA as needed OR on site in one of those locations where you will be required to be in-office 3 days/week. We're looking forward to hearing how you can contribute to our team and mission. Join us in shaping the future of our company and making a real impact every day. What We Offer:
A chance to be part of a vibrant small-company culture where your work can directly impact bringing new medicines to patients. Competitive salary and benefits package. Opportunities for professional growth and development. Apply for this job #J-18808-Ljbffr