Aaas Bothell , WA 98021
Posted 2 months ago
ROLE SUMMARY
The role supports a senior regulatory professional by executing against the global regulatory plan for one or more products. This positionrepresents
Regulatory on cross-functional teams and manages the development and preparation of regulatory documentation to regulatory authorities.
ROLE RESPONSIBILITIES:
Provide regulatory representation at cross-functional team meetings, including tactical support and clarity on regulatory expectations and timelines
Prepare, maintain and/or coordinate global regulatory submissions (INDs, CTAs, marketing applications) in accordance with applicable regulations
Understand and can challenge scientific arguments, identifies regulatory scientific data needs and solves regulatory issues.
Serve as primary contact to FDA (or other relevant regulatory authorities) for routine communications in support of submissions
Assist in preparation for and participate in regulatory authority meetings including preparation of briefing packages and strategy for meetings, inspections, advisory committee meetings, and response to agency letters pertaining to the assigned products/teams
Work with contract research organizations for ex-US regulatory submissions
BASIC QUALIFICATIONS
Bachelor's degree in scientific discipline and a minimum of 5 years regulatory experience; or Master's degree with minimum 3+ years experience
Oncology experience preferred
Solid knowledge and understanding of the drug development process and regional regulatory requirements
Experience in the preparation/submission of regulatory documentation to support regulatory submissions
Excellent oral and written communication skills
Strong technical/analytical skills to identify and solve problems independently
Proven ability to manage multiple projects, identify and resolve regulatory issues
Willingness to work collaboratively
Self-motivated, assertive, and self-confident
Strong organizational skills in order to maintain a high level of productivity, innovation, and priority-setting
Ability to work under pressure, meeting time sensitive deadlines, while maintaining a high level of quality
Proactively seeks out and recommends process improvements
Enjoys working in a fast-paced, environment
PREFERRED QUALIFICATIONS
Advanced degree preferable e.g. PharmD
Relevant pharmaceutical experience
Demonstrated experience in regulatory affairs or compliance
Experience working cross-functionally on broad and strategic initiatives
The annual base salary for this position ranges from $88,300.00 to $147,100.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 12.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Regulatory Affairs
Aaas