Talent.com
Regulatory Affairs Strategy Manager (Oncology)
Regulatory Affairs Strategy Manager (Oncology)Exelixis • Alameda, CA, United States
Regulatory Affairs Strategy Manager (Oncology)

Regulatory Affairs Strategy Manager (Oncology)

Exelixis • Alameda, CA, United States
9 hours ago
Job type
  • Full-time
Job description

SUMMARY / JOB PURPOSE :

Responsible for managing and maintaining existing Investigational New Drug (IND), Clinical Trial Application (CTA), New Drug Application (NDA), and Biologics Licensing Application (BLA) submissions and preparing amendments in compliance with guidelines and regulations. Coordinates, compiles, and tracks product applications and submissions to regulatory agencies. Assists senior regulatory leaders with the development of documents to support desigations and other health authority programs and requirements, health authority responses, and global regulatory planning.

ESSENTIAL DUTIES AND RESPONSIBILITIES :

  • Review clinical site regulatory documents to provide Regulatory approval to ship investigational product.
  • Track safety reports and coordinate submissions to US INDs.
  • Assist Project Team Regulatory Representative in preparing routine IND, NDA and BLA submissions and ex-US clinical trial applications, tracking submission progress, and archiving regulatory submissions and correspondence.
  • Assist with developing and implementing strategies to ensure compliance with HA requirements.
  • Respond to requests for information from regulatory bodies.
  • Serve as liaison with FDA.
  • Work collaboratively with consultants and contractors to accomplish regulatory activities and submissions.
  • Contribute to department initiatives.

SUPERVISORY RESPONSIBILITIES :

  • None
  • EDUCATION / EXPERIENCE / KNOWLEDGE & SKILLS :

    Education / Experience :

  • Bachelor's degree in related discipline and a minimum of seven years of related experience; or,
  • Master's degree in related discipline and a minimum of five years of related experience; or,
  • PhD degree in related discipline; or,
  • Equivalent combination of education and experience.
  • Experience / The Ideal for Successful Entry into Job :

    Knowledge / Skills :

  • Works independently and with others to contribute to plans, complete tasks and achieve results within established timelines. Takes pride in delivering high quality work.
  • Gathers, maintains and applies regulatory knowledge to complete routine work.
  • Provides verbal and written communications that are clear and easy to understand. Provides timely and appropriate information updates to departmental management and colleagues.
  • Good interpersonal skills, understanding of differing views; participates in reaching an agreed upon resolution.
  • Works collaboratively with team members to achieve common objectives.
  • Applies knowledge of organizational objectives and adopts an analytical approach to solve problems relevant to the role.
  • Leads self by managing and executing own work, acts with integrity and builds trust with colleagues.
  • JOB COMPLEXITY :

  • Capable of following predefined procedures for specific tasks.
  • Capable of identifying task-related challenges and prioritizing activity accordingly.
  • Identifies and escalates issues that may have a broader impact.
  • Implements solutions to address any task-related challenges.
  • WORKING CONDITIONS :

  • Travel approximately 10%
  • #LI-MB1

    If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us!

    Our compensation reflects the cost of labor across severalU.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this positionis $124,500 - $177,000 annually. The base pay range may take into account the candidate's geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate's geographic region, job-related knowledge, skills, experience and internal equity, among other factors.

    In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.

    DISCLAIMER

    The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.

    We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.

    Create a job alert for this search

    Regulatory Manager • Alameda, CA, United States

    Related jobs
    Director, Biocompatibility & Regulatory Strategy

    Director, Biocompatibility & Regulatory Strategy

    Abbott Laboratories • Santa Clara, CA, United States
    Full-time
    A global healthcare company is seeking a Director of Biocompatibility in Santa Clara, California.This role is responsible for managing biocompatibility evaluations for medical devices, ensuring com...Show more
    Last updated: 3 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
    Senior Director Regulatory Affairs

    Senior Director Regulatory Affairs

    EPM Scientific • San Francisco County, CA, United States
    Full-time
    The Senior Director will lead global regulatory strategy and operations across development pipeline.Developing and executing regulatory strategies. Overseeing submissions : INDs, CTAs, NDAs, BLAs, MA...Show more
    Last updated: 20 days ago • Promoted
    Global Fintech Regulatory Strategy Director

    Global Fintech Regulatory Strategy Director

    The MENA Catalysts, Inc. • San Francisco, CA, United States
    Full-time
    An innovative firm seeks a Senior Director of Fintech Legislative and Regulatory Affairs to shape the future of fintech in the Middle East. This role involves crafting regulatory strategies, managin...Show more
    Last updated: 2 hours ago • Promoted • New!
    Regulatory Affairs Manager

    Regulatory Affairs Manager

    Katalyst CRO • San Francisco, CA, United States
    Full-time
    Quality Assurance & Regulatory Affairs Manager, San Francisco, CA.IDE, 510(k), De Novo) and post-market requirements.Serve as the primary point of contact with the U. Food and Drug Administration (F...Show more
    Last updated: 8 days ago • Promoted
    Regulatory Affairs Manager – Heart Failure (on-site)

    Regulatory Affairs Manager – Heart Failure (on-site)

    Abbott Laboratories • Pleasanton, CA, United States
    Full-time
    At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Career development with an international company where you can grow th...Show more
    Last updated: 30+ days ago • Promoted
    Manager, Regulatory Affairs

    Manager, Regulatory Affairs

    Gilead Sciences, Inc. • Foster City, CA, United States
    Full-time +1
    At Gilead, we’re creating a healthier world for all people.For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapi...Show more
    Last updated: 30+ days ago • Promoted
    CMC Regulatory Dossier Mgmt Director

    CMC Regulatory Dossier Mgmt Director

    Exelixis • Alameda, CA, United States
    Full-time
    This role provides PSC Regulatory expertise and leadership for biologics and Bioconjugates commercial and development projects. Responsible and accountable for leading development of high-quality, p...Show more
    Last updated: 7 days ago • Promoted
    Director, Regulatory Affairs

    Director, Regulatory Affairs

    Septerna • San Francisco, CA, United States
    Full-time
    Septerna – Director of Regulatory Affairs.Septerna is a biotechnology company based in South San Francisco, CA, focused on developing life‑changing medicines. We aim to become the industry‑leading G...Show more
    Last updated: 11 days ago • Promoted
    Global Regulatory Leader - Oncology, IND / CTA Strategy

    Global Regulatory Leader - Oncology, IND / CTA Strategy

    Summit Therapeutics, Inc. • Menlo Park, CA, US
    Full-time
    A leading biotech firm is seeking a Senior Director, Regulatory Affairs – Global Regulatory Leader to develop strategies for IND / CTA approvals and oversee global marketing applications in oncology....Show more
    Last updated: 14 hours ago • Promoted • New!
    Senior Regulatory Lead, Virology Strategy & Submissions

    Senior Regulatory Lead, Virology Strategy & Submissions

    Gilead Sciences • San Francisco, CA, US
    Full-time
    A leading biopharmaceutical company in San Francisco seeks an Associate Director in Regulatory Affairs - Virology to define regulatory strategies, manage submissions, and represent the company in n...Show more
    Last updated: 14 hours ago • Promoted • New!
    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
    Regulatory Specialist (Hybrid Opportunity)

    Regulatory Specialist (Hybrid Opportunity)

    Stanford University • Stanford, CA, US
    Full-time
    The Blood & Marrow Transplantation and Cellular Therapy (BMT-CT) Division.Clinical Trials Regulatory Specialist II position to support a very active clinical trials faculty.The position will antici...Show more
    Last updated: 4 days ago • Promoted
    Global Regulatory Strategy Director - Oncology

    Global Regulatory Strategy Director - Oncology

    Summit Therapeutics Sub, Inc. • Menlo Park, CA, United States
    Full-time
    A leading biopharmaceutical company located in California is seeking a Senior Director of Regulatory Affairs.This role is pivotal in developing global regulatory strategies for oncology products, e...Show more
    Last updated: 1 day 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: 22 days ago • Promoted
    Head of CMC Regulatory Affairs – Strategy and Operations

    Head of CMC Regulatory Affairs – Strategy and Operations

    Gilead Sciences, Inc. • Foster City, CA, United States
    Full-time
    Oversee digital modernization of core CMC RA platforms (e.RIM) and integration across systems.Stand up for CMC RA (with enterprise thinking) and oversee a digital / AI fluency and enablement team ali...Show more
    Last updated: 3 days ago • Promoted
    Associate Director, Regulatory Affairs - Oncology

    Associate Director, Regulatory Affairs - Oncology

    Gilead Sciences, Inc. • Foster City, CA, United States
    Full-time
    Regulatory Affairs or other relevant industry experience.Degree in a scientific field is preferred.Responsible for preparing and / or overseeing the preparation of technically complex regulatory subm...Show more
    Last updated: 30+ days ago • Promoted
    Senior Director, Regulatory Affairs - Global Regulatory Leader

    Senior Director, Regulatory Affairs - Global Regulatory Leader

    Summit Therapeutics, Inc. • Menlo Park, CA, United States
    Full-time
    Senior Director, Regulatory Affairs – Global Regulatory Leader.Palo Alto, CA / Miami, FL / Princeton, NJ onsite.Ivonescimab, known as SMT112, is a novel, potential first-in-class investigational bi...Show more
    Last updated: 2 days ago • Promoted