Senior Director, Global Regulatory Strategy Lead

Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential.  Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you're ready to join us at the edge of something unstoppable, let's make a profound impact together for our patients, for your career, for what's beyond. You can view our latest corporate deck and other presentations here. About the Role >>> Senior Director, Global Regulatory Strategy Lead - Regulatory AffairsAs the Senior Director, Global Regulatory Strategy Lead - Regulatory Affairs reporting to the Senior Vice President of Regulatory Affairs, your responsibilities will include the following: Lead the development of the New Drug Application (NDA)  Lead the development and execution of innovative regulatory strategies supporting Olema productsRepresent Regulatory Affairs on cross-functional teams as the subject matter expert and provide regulatory guidance and oversight to the global project teams, Study Execution Teams, and the Executive CommitteeProvide strategic and tactical guidance and lead the development of regulatory submissions (INDs, CTx, briefing documents, IB, NDA, BLA, DMF, IMPD etc.) This role is based out of either our Boston, MA or San Francisco, CA office and will require domestic and international travel up to 20%. Your work will primarily encompass: Lead the development and submission of the NDA for the company's lead programDevelop innovative global regulatory strategies for the Olema portfolio of products, in clinical development and life-cycle management, as needed Represent Regulatory Affairs on cross-functional teams as the SME and provide regulatory guidance and oversight to the global project teams, Study Execution Teams, and the Executive committee Stay abreast of the regulatory landscape and regulatory requirements impacting drugs, biologics and devices Provide strategic and tactical guidance and lead the development of regulatory submissions (INDs, CTX, briefing documents, IB, NDA, BLA, DMF, IMPD etc.) Represent Olema with Global Health Authorities and lead Agency interactions to achieve company objectives Identify gaps and develop risk mitigation strategies for the regulatory submissions Ensure Olema's regulatory activities are robust and are in compliance with Health Authority (HA) regulatory requirements Coordinate and maintain all HA reporting schedules in collaboration of cross-functional teams Be flexible to adapt and accommodate additional duties as assigned And will also include: Lead the development of Regulatory Affairs department policies, SOPs, and work instructions Provide Regulatory guidance and leadership to cross-functional teams on software implementation for Regulatory dossiers (e.g., Veeva) Keep the Leadership and the organization fully informed of the regulatory landscape, including HA initiatives and impact on Olema's programs Lead the global regulatory team(s) and ensure execution of the Regulatory strategies to achieve the company objectives Mentor and develop other regulatory colleagues in the department Support SVP Regulatory Affairs, as required Ideal Candidate Profile  >>> Innovative Experienced Regulatory Strategy Leader A love of challenging, important work. We are a pragmatic team, driven to imagine and develop meaningful therapies for improving lives. All employees within our company play a unique and crucial role in our success, both in accomplishing our mission and building a positive company culture. As such, we are looking for someone with the right combination of knowledge, experience, and attributes for this role. KnowledgeBachelor's degree in a scientific discipline Advanced degree in scientific discipline Masters, Pharm D or PhD is preferred  ExperienceMinimum of 12 years' experience in Regulatory Affairs in Pharma/Biotech Minimum of 3 years direct leadership experienceExperience with development and execution of regulatory strategies in Oncology Therapeutic area is strongly preferred Strong understanding of US FDA, EU and international pharmaceutical guidance, regulations, drug development process, and industry standard practicesExperience with major regulatory submissions (e.g. New Drug Applications (NDA/NDS/MAA), is a must  Experience in strategic problem-solving and negotiation with Health Authorities and leading internal teams on the regulatory strategy for a given product is requiredAbility to work in a fast-paced environment in a hands-on fashion Excellent oral, written, and presentation skills, with experience presenting to the leadership teamsDemonstrated proficiency in organizational awareness, including experience working cross-functionally representing the Regulatory Affairs function and on global teamsExcellent planning and organizational skills and ability to work simultaneously on multiple projects with tight timelinesExperience in all phases of development and post marketing activities is highly preferredDemonstrated ability to analyze and interpret efficacy and safety dataStrong understanding of regulatory operational activitiesAttributesSelf-starter Flexible and proactive, with the ability to manage multiple projects and successfully adapt to changing business needs and priorities Team Player On site presence at the headquarter is required (minimum 2 days a week)The base pay range for this position is expected to be $275,000-$290,000 annually, however the base pay offered may vary depending on location, market, job related knowledge, skills and capabilities, and experience. The total compensation package for this position also includes equity, bonus, and benefits.#LI-MK1 Important Information >>> We provide equal opportunity to all employees and applicants for employment and believe that great ideas and discoveries come from a mix of expertise, background, and experience. Olema is building a culture where the value of difference is celebrated.We offer a competitive compensation and benefits package, seeking to provide an open, flexible, and friendly work environment to empower employees and provide them with a platform to develop their long-term careers. A Summary of Benefits is available for all applicants.Please note: Olema doesn't accept agency resumes and is not responsible for any fees related to unsolicited resumes. Thank you.Fraud Alert:  We are aware of employment scams where individuals pose as representatives of Olema Oncology and make false use of our company name to defraud job seekers. To protect yourself, please note that Olema's official email addresses end in Our official corporate website is ; our careers page is ; our LinkedIn page is  Please visit these links for official information from Olema. Communication from any other variant is fraudulent. Olema does not conduct interviews via text message/messaging platforms, will not ask you to download anything as part of your interview, will never request any form of payment, provide upfront payments of any kind, and does not make job offers without an in-person interview.