Senior Director, Global Regulatory Strategy (Boston)

Senior Director, Global Regulatory Strategy

Join to apply for the Senior Director, Global Regulatory Strategy role at Olema Oncology

Senior Director, Global Regulatory Strategy

2 weeks ago Be among the first 25 applicants

Join to apply for the Senior Director, Global Regulatory Strategy role at Olema Oncology

Direct message the job poster from Olema Oncology

Olema Oncology is a cancer medicines company dedicated to impacting breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a differentiated oral medicine known as a complete estrogen receptor antagonist (CERAN) initially in development for metastatic breast cancer. Our pipeline also includes OP-3136, a potent, selective oral inhibitor of the KAT6 pathway. At Olema, we are building a focused team committed to our mission with intention and clarity. Working alongside a talented passionate group of leaders and advisors, we strive to create better medicines that aim to help patients feel better, longer. For more information, visit us at .
About the Role >>> Senior Director, Global Regulatory Strategy
As the Senior Director, Global Regulatory Strategy - Regulatory Affairs reporting to the Vice President of Regulatory Affairs and Quality Assurance, your main responsibilities will include the following:

• Lead the development and execution of innovative regulatory strategies supporting Olema products
• Represent 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 Committee
• Provide 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 our Boston, MA o r San Francisco, CA office.
Your work will primarily encompass:

• Develop innovative global regulatory strategies for the Olema portfolio of products, in clinical development and life-cycle management, as needed
• Represent Regulatory Affairs as the SME across cross-functional teams and provide regulatory guidance/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 (e.g., companion diagnostics)
• Be accountable for, provide both 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
• Proactively identify gaps and develop risk mitigation strategies for regulatory submissions in alignment with the team(s) and management
• Ensure Olema’s regulatory activities are robust and in compliance with Health Authority (HA) regulatory requirements
• Coordinate and maintain all HA reporting schedules in collaboration of cross-functional teams
• Serve as the point of contact with external parties and vendors supporting regulatory activities (e.g., CROs, contractors etc)
• Participate in and contribute to cross-functional and departmental objectives
• Maintain flexibility to adapt and accommodate additional duties as assigned
  

And will also include the following:

• 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, policies and their potential impact on Olema’s programs
• Lead the global Regulatory team(s) and ensure execution of the regulatory strategies to achieve company objectives
• Mentor and develop colleagues in the Regulatory department
  

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.
Knowledge:

• Bachelor’s degree in a scientific discipline
• Advanced degree in scientific discipline Masters, Pharm D or PhD is preferred
  

Experience:

• 10-12 years’ experience in Regulatory Affairs in Pharma/Biotech
• Minimum of 3 years direct leadership experience
• Strong negotiation skills with health authorities (viz., FDA, EMA, Health Canada, etc.) as well as submissions (IND/CTx to NDA/BLA or Marketing Applications)
• Experience in Oncology Therapeutic area is strongly preferred
• Experience with development and execution of regulatory strategies in Oncology TA is strongly preferred
• Ability to work in a fast-paced environment in a hands-on fashion
• Excellent oral, written, and presentation skills
• Strong organizational skills
  

Attributes:

• Self-starter
• Flexible and proactive, with the ability to manage multiple projects and successfully adapt to changing business needs and priorities
• Ability to travel domestically and internationally, as required (approximately 25%)
  

The base pay range for this position is expected to be $275,000 - $287,000 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.
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.
Additional Note/Fraud Alert : Olema will not conduct interviews via text message or messaging platforms and will not ask you to download anything as part of your interview. Though we use third party tools to help with advertising our jobs, please be vigilant in checking that the communication is in fact coming from Olema.

Seniority level

• Seniority level

  Director

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research, Science, and Manufacturing

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Olema Oncology by 2x

Get notified about new Legal Director jobs in Boston, MA .

Waltham, MA $266,000 - $326,000 1 week ago

Associate Legal Director, Commercial Counsel

Boston, MA
$215,000.00
-
$275,000.00
2 months ago

Boston, MA
$160,000.00
-
$200,000.00
1 month ago

Director/Senior Director, Corporate Counsel

Director, Practice Operations - Litigation

Senior R&D Legal Counsel, Director (Hybrid)

Eastern Region, Regulatory & IA Director - Hybrid to Andover, MA

Andover, MA
$156,960.00
-
$215,820.00
1 month ago

Director of Privacy & Senior Legal Counsel

Associate Director/Director, Intellectual Property (Patent Counsel)

Senior Regulatory Legal Counsel, Director (Hybrid)

Boston, MA
$85,000.00
-
$125,000.00
5 days ago

VP, Corporate Counsel, Jennison Associates

Boston, MA
$216,000.00
-
$292,200.00
3 days ago

Senior Director, Senior Corporate Counsel

Director, Assistant General Counsel – Securities

Associate Director - Global Regulatory Lead, GI & Inflammation

Director, Global Regulatory Lead, GI & Inflammation

Vice President Legal Counsel - US Institutional Product Team

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