Regulatory Strategy, Director (Bay Area, Boston) at Premier Research | Torre
Regulatory Strategy, Director (Bay Area, Boston)
trending_up Invest in Torre
Premier Research

Regulatory Strategy, Director (Bay Area, Boston)

Premier Research
Emma
Emma
Emma highlights
This highlight was written by Emma’s AI. Ask Emma to edit it.
Freelance
Recurrent
Compensation USD150k/year
location_on
San Francisco Bay Area, CA, USA
Shared by
Julien PETIT
 3 months ago

Responsibilities

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.- We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.- Your ideas influence the way we work, and your voice matters here.- As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.What You'll Be DoingDevelop and execute regulatory program strategies and contingencies for assigned projectsLead both US and ex-US regulatory teams on assigned projectsDevelop and implement creative approaches to ensure regulatory successProvide efficient and effective regulatory representation with clients as well as across the organization and act as a key player in interactions with the Food and Drug Administration (FDA) and other regulatory agenciesServe as the primary point of contact and interface for FDA/EMA/national agencies on assigned projectsLead the preparation of submissions, which may include INDs, briefing documents, orphan drug applications, breakthrough designations, and NDAs/BLAs/MAAs and othersWhat We Are Searching ForBachelor’s degree, or international equivalent from an accredited institution, in science or health related field; Master’s Degree or PhD preferred12+ years of experience rmaceutical, biotechnology or device/diagnostics industry; an advanced degree will be considered in lieu of a portion of industry experience8-9 years progressive regulatory affairs experience (US and/or ex-US) for a CRO/biotech/pharma of which 4+ years has been as a consultantDemonstrated experience interacting with the Food and Drug Administration (FDA), European Medicines Agency (EMA), and other regulatory agenciesDemonstrated leadership experience in the opening of INDs and submission and approvals of NDAs/ BLAs/MAAsExpert in the drug development process with experience in multiple phases (early and late stage, post-approval) in various therapeutic areas and product types (drugs, biologics, drug-drug combinations, drug-device combination products)Preferred Location: San Francisco or BostonPremier Research is dedicated to providing compensation that is fair and competitive with market standards. The annualized minimum base pay for this role is $150,000.00 USD. The actual salary will be influenced based on a variety of factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. We also offer a comprehensive benefits package, which may include health insurance, retirement plans, and paid time off.Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status
This job post is closed.