Associate Director, Regulatory Affairs CMC

Olema Oncology • Boston, MA

2d • $190,000 - $205,000 • Onsite

About The Position

As the Associate Director, Regulatory Affairs CMC, reporting to the Senior Director, Regulatory Affairs CMC, you will be responsible for developing and executing the CMC regulatory strategies for Olema product(s) in development and post-approval. You will ensure these strategies are aligned with Health Authority requirements globally and provide guidance and oversight for development of high quality and on-time CMC sections of the regulatory submissions. In addition, you will provide CMC regulatory strategy support and guidance to cross-functional teams within the organization.
This role is based out of our San Francisco, CA office and will require 10% travel.

Requirements

• Bachelor's degree is required, preferably in a scientific field; advanced degree is a plus
• Excellent knowledge of current CMC regulations and regulatory procedures
• Excellent working knowledge of international regulatory requirements and environment, including an understanding of GXP
• Deep understanding of clinical trial requirements for initial INDs/CTAs for all development phases early to late-stage
• Minimum 8 years of experience working in clinical research, biotech, and/or pharmaceutical company, with minimum 6 years of Regulatory Affairs experience within clinical research or pharmaceutical
• Experience in small molecule drug development required; experience in the oncology therapeutic area is a plus
• Global CMC regulatory experience for clinical trials is required
• Experience with eCTD requirements and electronic submissions
• Strong business acumen and ability to successfully work with international and cross functional partners
• Very strong strategic skills including creativity and effectiveness in identifying and addressing major strategic challenges (e.g., new competition, shifting market environment) and the ability to balance short-term needs with long-term vision
• Proven ability to deliver on goals within a cross-functional team/partnership environment with a high level of professionalism
• Excellent verbal, written and presentation skills
• Able to analyze, define and effectively convey difficult and complex issues in a way that accurately and persuasively communicates the issues to internal and external stakeholders
• Fosters open communication. Listens and facilitates discussion
• Maintain learner mindset, with an ability to adapt to an ever-changing environment
• Proven ability to prioritize and manage multiple tasks and requests efficiently

Nice To Haves

• Post approval (commercial) experience is a plus
• Experience with international regulatory submissions and processes is a strong plus

Responsibilities

• Provide CMC regulatory expertise for global development and registration programs (e.g., INDs, CTAs, BLAs and MAAs)
• Support regulatory agency interactions to ensure alignment on CMC strategies for initial INDs/CTAs, marketing registration applications, supplements and variations.
• Provide CMC support on the global regulatory plan, development plans/clinical study designs and risk assessments
• Proactive and effective communication of critical issues and potential mitigations with teams, senior management and key stakeholders in a timely manner
• Assess and communicate regulatory requirements to ensure all development activities are in compliance with applicable regulations and guidelines
• Manage and ensure compliance with all reporting requirements, including annual and periodic reports.
• Collaborates well with internal and external teams (CMC, QA, Supply Chain, RA etc)
• Assist with the planning, compilation, review, approval and submission of high-quality CMC related sections of regulatory submissions, including responses to questions from various regulatory authorities, working in collaboration with partners in Research, Process Sciences, Manufacturing, QC/QA, Global Supply Chain and other business partners
• Provide regulatory support for relevant quality systems such as change control, discrepancy management, and inspection management. Assess proposed manufacturing process changes and provide strategic regulatory guidance to enable global implementation
• Support interactions with regulatory agencies during inspections
• Maintain up to date knowledge and expertise with FDA/EMA regulations, ICH guidelines and other international regulatory regulations and guidelines, as needed to support global programs

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 101-250 employees