Associate Director, Regulatory Affairs - San Diego, CA

Mirador Therapeutics, Inc.•San Diego, CA

1d•$170,000 - $200,000•Onsite

About The Position

Mirador is a next-generation precision medicine company focused on immunology and inflammation. The company’s Mirador360 TM precision development engine leverages the latest advances in human genetics and cutting-edge data science to rapidly advance new precision medicines for patients living with chronic immune-mediated inflammatory and fibrotic diseases. Launched in 2024, Mirador has raised over $400 million from leading life sciences investors and is based in San Diego, CA. Summary The Associate Director of Regulatory Affairs, within the Regulatory Affairs and Quality organization, is responsible for development and implementation of regulatory affairs strategy as a member of multi-disciplinary pharmaceutical product development teams.

Requirements

Bachelor's degree required, with an advanced scientific degree (PhD, PharmD) strongly preferred.
8 or more years of experience in Regulatory Affairs; experience in therapeutic areas of company focus is a plus.
Regulatory Affairs experience with multiple therapeutic modalities; e.g., biologics, drug/device combination products.
Experience with complex clinical trial designs.
Unquestionable integrity, be able to inspire trust and exhibit the highest ethical standards.
Excellent communication, verbal and written, and interpersonal skills with strong ability to interact with internal teams and partners across all levels of the organization.
Ability to effectively present information and respond to questions from all levels of the organization.
Sense of urgency, flawless execution with intense focus on accuracy and accountability.
Self-starter, highly motivated, assertive, driven, and hands-on leader.
Ability to multi-task in a fast-paced, entrepreneurial, smaller company environment.
Operate collaboratively with colleagues across functional areas in a science-driven environment.
Ability to work well under pressure and meet time sensitive deadlines.
Ability to work across locations and time zones.
Highly proficient using Veeva, Microsoft Word, Excel, PowerPoint, Project, and SharePoint; or similar applications and systems.
Strong financial business acumen and analytical skills; ability to develop and manage expenditures in accordance with budget.
Travel up to 5-10% may be required to meet with vendors and regulators.

Nice To Haves

experience in therapeutic areas of company focus is a plus.
advanced scientific degree (PhD, PharmD) strongly preferred.

Responsibilities

Represent Regulatory Affairs in assigned project meetings and provide regulatory guidance to cross-functional project teams as appropriate; leverage experience in drug and device regulatory affairs to provide guidance to colleagues for preparation of regulatory documents.
Serve as Regulatory Affairs contact for external parties (for example, CROs) involved in the conduct of global clinical trials.
Develop and implement global regulatory strategy for drug and device submissions to support clinical trials and registration in accordance with applicable regulations/guidelines (for example, U.S. FDA, EMA, ICH, ISO, etc.).
Plan, prepare, author, and/or review submissions (for example, IND, CTA, BLA, NDA, MAA, IDE, PMA) to health authorities to support clinical trials, registration, maintenance of registration, and labeling of pharmaceutical products.
Oversee interactions with vendor for electronic submissions.
May serve as primary liaison with FDA (and other health authorities, as appropriate) for day-to-day interactions.
Contribute to the development of competitive regulatory strategies that expedite development, maximize the probability of success, and mitigate risks.
Communicate project updates and risks to senior Regulatory management and stakeholders across the organization.
Tracking regulatory commitments and deliverables while coordinating with internal and external staff to ensure timely submissions.
Coordinate and prepare responses to requests for information from health authorities.
Prepare meeting requests, briefing documents, coordinate and prepare teams for meetings with health authorities.
Provide input into development of internal documentation practices and systems.
Monitor, analyze, and disseminate intelligence on regulatory matters that may affect ongoing development programs.
Participate in due diligence evaluations of potential in-license/partnering opportunities.
Initiate and contribute to the development of policies and procedures in alignment with GxPs, Guidance, and corporate objectives.