Director/Associate Director, Regulatory Affairs

ORIC Pharmaceuticals • San Diego, CA

6d • Onsite

About The Position

The position is responsible for supporting and leading activities within the Regulatory Affairs department to support the clinical development of oncology products at ORIC. This involves working closely with cross-functional colleagues including regulatory operations, quality, CMC, nonclinical and clinical team members. The successful candidate will be a highly motivated team player with the ability to plan proactively, work independently, think strategically, and execute assigned projects effectively.

Requirements

• Bachelor’s degree in a scientific or related field, advanced degree preferred.
• At least 8+ years of regulatory affairs experience in the pharmaceutical or biotechnology industry.
• Experience in preparing regulatory submissions, e.g., IND, DSUR, CTA, FDA meeting request.
• Demonstration of excellent communication and interpersonal skills, with the ability to effectively collaborate with internal and external stakeholders.
• Excellent writing and editorial skills, ability to collaborate on development of high-quality clinical-regulatory documents, e.g., investigator brochures, meeting request/package.
• Strong organizational skills, with the ability to manage multiple projects simultaneously and meet deadlines.
• Strong attention to details with accuracy and quality.
• A good scientific background and understanding with the ability to acquire therapy area and regulatory knowledge.
• Knowledgeable in global regulatory requirements and guidelines (e.g., FDA guidance, ICH) and gathering regulatory intelligence.
• Proficient in computer literacy, e.g., Microsoft Word, Excel, PowerPoint.

Responsibilities

• Support regulatory submission and strategic direction for all ORIC’s development programs.
• Lead to deliver high quality and timely regulatory submissions in alignment with corporate goals, and in compliance with all applicable regulatory requirements.
• Coordinate and collaborate regulatory activities across functions within ORIC, i.e., regulatory operations, quality, CMC, nonclinical, clinical.
• Responsible for the creation, assembly, review and/or oversight of complex regulatory submissions which require interaction with cross-functional teams to ensure optimal execution.
• Ensure consistency, completeness and adherence to standards for all regulatory submissions.
• Represent ORIC to develop and maintain strong relationships with the FDA and other global regulatory agencies.
• Grow corporate, project and industry knowledge by reviewing and analyzing current regulatory issues, guidance, initiatives and communicating regulatory intelligence internally.
• Participate in providing strategic input on regulatory activities in support of the product development plan.
• Participate in the development and review of standard operating procedures to ensure compliance with current regulatory requirements.
• Perform all duties in keeping with the Company’s core values, policies and all applicable regulations.

What This Job Offers

• Job Type: Full-time
• Career Level: Director