Talent.com
Director_Sr. Director, Regulatory Affairs
Director_Sr. Director, Regulatory AffairsAbdera Therapeutics • South San Francisco, CA, US
Director_Sr. Director, Regulatory Affairs

Director_Sr. Director, Regulatory Affairs

Abdera Therapeutics • South San Francisco, CA, US
30+ days ago
Job type
  • Full-time
Job description

Job Description

Job Description

Who we are

Abdera Therapeutics Inc. is a precision oncology company developing next-generation targeted radiation therapies- one of the most cutting-edge and highly promising areas of drug development. The company is built on a proprietary modular technology platform optimized for the delivery of radioisotopes to selectively destroy tumor cells while sparing healthy cells. Abdera is using this platform to enable the rapid development of a broad range of safe and efficacious therapies serving cancer patients with limited treatment options.

Abdera Therapeutics is growing rapidly and seeking key new team members who thrive at the cutting-edge of innovation. Come join us and be a part of the ground-breaking team set to unlock the power of targeted radiotherapy!

What we look for

At Abdera Therapeutics, we are looking for curious and committed individuals who are ready for the opportunity to transform the way people living with cancer can be treated. We are devoted to advancing novel treatment options that offer new hope to families facing devastating diagnoses. We are in search of team members who work collaboratively with a diverse group of colleagues, respectfully engaging one another while collectively and inclusively tackling any challenges we may face. We are building an exciting and fast-paced company passionate about discovering and developing tomorrow’s most innovative cancer therapies.

For this role we are seeking a seasoned and strategic regulatory affairs leader to drive our mission of transforming cancer care through targeted radiotherapy. The ideal candidate will bring deep expertise in FDA regulatory processes, IND preparation, and global drug development, with a strong foundation in regulatory affairs (radiopharmaceuticals is a plus). This role demands a proactive, collaborative professional who thrives in a fast-paced, innovation-driven environment and can lead cross-functional teams with clarity and confidence. We’re looking for someone who combines scientific rigor with emotional intelligence, and who is passionate about delivering hope to patients through breakthrough therapies.

Salary range : $200 - 270K

This is a hybrid schedule with 3 days per week in our SSF office.  We will consider remote for those with a radiopharmaceutical background

Principal Responsibilities

  • Develop and implements regulatory strategies and contingencies for assigned programs, in order to support Abdera’s development objectives.
  • Lead and prepare FDA submissions.
  • Participate in global project team meetings provide regulatory support and guidance and manage day-to-day regulatory activities.
  • Provides guidance and expertise to senior management and other departments on all regulatory issues for the strategic development, planning, compilation and submission for all regulatory filings.
  • Serve as the primary contact with FDA and liaise, negotiate and orchestrate all interactions with FDA.
  • Provide mentorship to multidisciplinary teams on the content, format, style and architecture of an Investigational New Drug (IND) application.
  • Edit or lead the editing of scientific sections of regulatory documentation against the regulatory requirements. Assist with the writing, review and preparation of an IND application.
  • Manage the organization, preparation and review of IND amendments, annual reports and other regulatory documents and correspondence.
  • Participate in due diligence activities and communicate regulatory risks before products / devices development, acquisition or in-licensing of new product or devices.
  • Provides support on labeling and advertising matters.
  • Maintain knowledge of regulatory environment, global regulations and guidance
  • Contribute to the development and maintenance of Regulatory Affairs working practices and procedures
  • Support in the preparation of the Regulatory Affairs department budget

Qualifications, Education & Experience

  • Bachelor’s degree in chemistry, biochemistry, pharmacy, pharmacology, or related scientific discipline required.
  • Master’s Degree, PharmD or PhD preferred.
  • 7-10+ years of relevant experience in a similar role within the biotechnology or pharmaceutical industry
  • 5-7 + years in regulatory affairs
  • Radio expertise a plus
  • Ability to interpret and understand US regulations governing pharmaceutical industry.
  • Comprehensive understanding of drug development and related concepts, such as clinical trial design, statistics, and clinical pharmacology.
  • Strong written, verbal, and interpersonal communication skills, with the ability to effectively interact with individuals at all levels across organization.
  • Prior experience with FDA submissions required.
  • Skills and Abilities

  • Ability to critically review regulatory scientific documents across non-clinical and clinical disciplines.
  • Builds a learning environment that recognizes the value of each contributor and promotes a solutions orientation.
  • Ability to constructively challenge, question, and provide creative suggestions for regulatory trial processes in order to create the most efficient and effective methods to deliver quality clinical trial services.
  • Willingness to collaborate with team to identify and implement in best practices for optimizing performance.
  • Naturally connects and builds strong relationships with others, demonstrating strong emotional intelligence and an ability to communicate clearly and persuasively.
  • Strong leadership skills in leading team members and vendors.
  • Demonstrated ability to manage and coordinate internal and external resources independent from managerial oversight.
  • Strong organizational, communication and interpersonal skills
  • Ability to prioritize, delegate and execute to meet project deadlines.
  • Proactive, innovative, with excellent problem-solving skills.
  • Excellent computer skills (Microsoft Office Suite, Project, Word, Excel, PowerPoint, Outlook, and IXRS / EDC platforms).
  • At ease in start-up environment and effectiveness to deliver in low-structured environments.
  • At Abdera, we recognize the importance of attracting and retaining the best talent, and we're committed to offering competitive compensation and comprehensive benefits tailored to your needs.

    Here’s what you can expect when you join our team in the U.S. :

  • Competitive Base Pay : Our expected base pay range for this position is $200 - $275k (USD), plus performance-based bonuses.
  • Comprehensive Benefits : Health, Dental, Vision, Prescription drug coverage, Basic Life and AD&D insurance, both Long-Term and Short-Term disability 16 paid company holiday, 20 days of PTO and 6 sick days to ensure your well-being, as well as a 401k plan with up to 3.5% company match, equity and bonus to help secure your financial future.
  • Personalized Pay : Your individual pay will be determined by your job-related skills, experience, and relevant education or training, ensuring you receive fair and competitive compensation.
  • Work-Life Balance : We also offer a hybrid work schedule with 3 days on-site along with development and growth opportunities.
  • At Abdera, we value our employees and strive to create an environment where you can thrive both professionally and personally. Join us and be part of a company that cares about your growth and well-being.
  • Abdera is an equal opportunity employer that is committed to diversity and inclusion in the workplace. At Abdera, we prohibit harassment of any kind and any form of discrimination including but not limited to discrimination based on race, color, sex, religion, marital status, sexual orientation, national origin, disability, veteran status, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

    This is applicable to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship.

    Powered by JazzHR

    FHjdJjlJpG

    Create a job alert for this search

    Director Regulatory • South San Francisco, CA, US

    Related jobs
    Associate Director CMC Regulatory

    Associate Director CMC Regulatory

    VirtualVocations • Fremont, California, United States
    Full-time
    A company is looking for an Associate Director, CMC Regulatory Strategy.Key Responsibilities Lead the planning, authoring, and review of regulatory submissions for various projects Provide in-de...Show more
    Last updated: 4 days ago • Promoted
    Pharmacy Director, Active License

    Pharmacy Director, Active License

    VirtualVocations • Fremont, California, United States
    Full-time
    A company is looking for a Director, Pharmacy Part B & Specialty Drugs.Key Responsibilities Lead specialty drug program design, execution, and monitoring across Medicare Advantage Develop and im...Show more
    Last updated: 3 days ago • Promoted
    Director, Regulatory Affairs

    Director, Regulatory Affairs

    Revolution Medicines • Redwood City, CA, US
    Full-time
    Director Of Regulatory Affairs.Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers...Show more
    Last updated: 30+ days ago • Promoted
    Regulatory Affairs CMC Director

    Regulatory Affairs CMC Director

    Exelixis • Alameda, CA, United States
    Full-time
    Provide Regulatory Affairs CMC expertise and leadership for global commercial and development projects.Develop strategic approaches to enable succesful Health Authority submissions and communicatio...Show more
    Last updated: 30+ days ago • Promoted
    Director / Senior Director, Regulatory Affairs (Clinical & CMC)

    Director / Senior Director, Regulatory Affairs (Clinical & CMC)

    Valid8 Financial, Inc. • San Francisco, CA, United States
    Full-time
    Director / Senior Director, Regulatory Affairs (Clinical & CMC).Director / Senior Director, Regulatory Affairs.This individual will oversee both Clinical and CMC regulatory functions, providing strat...Show more
    Last updated: 30+ days ago • Promoted
    Senior Manager Regulatory Affairs

    Senior Manager Regulatory Affairs

    VirtualVocations • San Francisco, California, United States
    Full-time
    A company is looking for a Senior Manager Regulatory Affairs - Labeling, Advertising and Promotions (Remote).Key Responsibilities : Guide and coordinate regulatory strategy for labeling, advertisi...Show more
    Last updated: 30+ days ago • Promoted
    Director / Senior Director, Regulatory Affairs Strategy

    Director / Senior Director, Regulatory Affairs Strategy

    Oruka Therapeutics • Menlo Park, CA, United States
    Full-time
    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...Show more
    Last updated: 30+ days ago • Promoted
    Senior Director, Global Regulatory Affairs Project Management

    Senior Director, Global Regulatory Affairs Project Management

    Revolution Medicines • San Francisco, CA, United States
    Full-time
    Senior Director, Global Regulatory Affairs Project Management.Be among the first 25 applicants.Revolution Medicines is a clinical-stage precision oncology company focused on developing novel target...Show more
    Last updated: 21 days ago • Promoted
    Senior Director of Drug Safety

    Senior Director of Drug Safety

    VirtualVocations • Fremont, California, United States
    Full-time
    A company is looking for a Senior Director, Drug Safety and Pharmacovigilance.Key Responsibilities Oversee the safety profile of assigned products from clinical development to post-approval safet...Show more
    Last updated: 4 days ago • Promoted
    Senior Director, Regulatory Affairs

    Senior Director, Regulatory Affairs

    Nava • Emeryville, CA, United States
    Full-time
    The Senior Director, Regulatory Affairs position provides regulatory oversight for multiple projects focused on non-clinical and clinical aspects of drug development and associated regulations.This...Show more
    Last updated: 15 days ago • Promoted
    Associate Director, Regulatory Affairs

    Associate Director, Regulatory Affairs

    Maze Therapeutics • San Francisco, CA, United States
    Full-time
    Join Maze Therapeutics as an Associate Director, Regulatory Affairs, where you will play a critical role in advancing our clinical-stage programs by providing regulatory expertise and executional l...Show more
    Last updated: 30+ days ago • Promoted
    Senior Director, Global Regulatory Strategy Lead - Regulatory Affairs

    Senior Director, Global Regulatory Strategy Lead - Regulatory Affairs

    Olema Oncology • San Francisco, CA, United States
    Full-time
    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 dev...Show more
    Last updated: 30+ days ago • Promoted
    Director of Regulatory Affairs (San Francisco, CA)

    Director of Regulatory Affairs (San Francisco, CA)

    Cedent • San Francisco, CA, United States
    Full-time
    Director of Regulatory Affairs (San Francisco, CA).This role provides global regulatory leadership and expertise to ensure compliance and successful submission of clinical regulatory filings.The po...Show more
    Last updated: 4 days ago • Promoted
    Director of CMC Drug Substance

    Director of CMC Drug Substance

    VirtualVocations • Santa Clara, California, United States
    Full-time
    A company is looking for a Director, CMC Drug Substance (Remote).Key Responsibilities Direct CMC drug substance development and manufacturing activities across multiple projects Lead strategy, p...Show more
    Last updated: 4 days ago • Promoted
    Director, Regulatory Strategy

    Director, Regulatory Strategy

    Exelixis • Alameda, CA, United States
    Full-time
    Responsible for driving the development and implementation of global regulatory strategies that align with asset and corporate goals as well as health authority requirements.Ensures timely preparat...Show more
    Last updated: 3 days ago • Promoted
    Sr. Regulatory Affairs Specialist

    Sr. Regulatory Affairs Specialist

    Calyxo, Inc. • Pleasanton, CA, United States
    Full-time
    The company was founded in 2016 to address the profound need for improved kidney stone treatment.Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resourc...Show more
    Last updated: 16 days ago • Promoted
    Director_Sr. Director, Regulatory Affairs

    Director_Sr. Director, Regulatory Affairs

    Abdera Therapeutics • South San Francisco, CA, US
    Full-time
    Quick Apply
    Who we are Abdera Therapeutics Inc.The company is built on a proprietary modular technology platform optimized for the delivery of radioisotopes to selectively destroy tumor cells while sparing hea...Show more
    Last updated: 30+ days ago
    Director, Regulatory Operations (Systems)

    Director, Regulatory Operations (Systems)

    Revolution Medicines • Redwood City, CA, United States
    Full-time
    The Director of Regulatory Information Management (RIM) will partner closely with the Senior Director and Head of Regulatory Operations and Planning to build, lead, and scale Revolution Medicines’ ...Show more
    Last updated: 20 days ago • Promoted