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Medical affairs Empleos en Santa clarita ca

Última actualización: hace 14 horas
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DIRECTOR, REGULATORY AFFAIRS

DIRECTOR, REGULATORY AFFAIRS

Revolution MedicinesCA, United States
204.000,00 US$–255.000,00 US$ anual
A tiempo completo
Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline com...Mostrar másÚltima actualización: hace 1 día
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ASSISTANT, TV BUSINESS AFFAIRS

ASSISTANT, TV BUSINESS AFFAIRS

LionsgateCA, United States
45.000,00 US$ anual
A tiempo completo
Lionsgate has an opening for a Coordinator to support two EVPs of Television Business Affairs.This opportunity provides an excellent learning experience for an individual with a strong interest in ...Mostrar másÚltima actualización: hace 1 día
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EXECUTIVE DIRECTOR, REGULATORY AFFAIRS CMC

EXECUTIVE DIRECTOR, REGULATORY AFFAIRS CMC

ExelixisCA, United States
A tiempo completo
This role provides CMC Regulatory expertise and leadership for commercial and development projects.This role leads all regulatory activities related to chemistry, manufacturing, and controls (CMC) ...Mostrar másÚltima actualización: hace 4 días
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Director / Senior Director, Regulatory Affairs

Director / Senior Director, Regulatory Affairs

Hobson PriorSan Mateo County, CA, United States
A tiempo completo
Hobson Prior is seeking a Director / Senior Director, Regulatory Affairs Labelling, Advertising, and Promotion to join the team. This role will focus on overseeing the labelling process for various ...Mostrar másÚltima actualización: hace 3 días
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DIRECTOR, REGULATORY AFFAIRS (ANIMAL HEALTH)

DIRECTOR, REGULATORY AFFAIRS (ANIMAL HEALTH)

Alveo TechnologiesCA, United States
196.686,00 US$–205.000,00 US$ anual
A tiempo completo
Alveo Technologies is the first company to make molecular detection and diagnostics universally accessible - on the farm, in the field, in the clinic, or in the manufacturing plant - helping preven...Mostrar másÚltima actualización: hace 4 días
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DIRECTOR, REGULATORY AFFAIRS : JOB ID - 1435

DIRECTOR, REGULATORY AFFAIRS : JOB ID - 1435

Ascendis PharmaCA, United States
200.000,00 US$–225.000,00 US$ anual
A tiempo completo
Denmark, Europe, and the United States.Today, we're advancing programs in Endocrinology Rare Disease and Oncology.Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, ...Mostrar másÚltima actualización: hace 1 día
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  • Nueva oferta
DIRECTOR GLOBAL REGULATORY AFFAIRS DIGITAL SOLUTIONS

DIRECTOR GLOBAL REGULATORY AFFAIRS DIGITAL SOLUTIONS

IntuitiveCA, United States
A tiempo completo
At Intuitive, we are united behind our mission : we believe that minimally invasive care is life-enhancing care.Through ingenuity and intelligent technology, we expand the potential of physicians to...Mostrar másÚltima actualización: hace 14 horas
Regulatory Affairs Specialist

Regulatory Affairs Specialist

Kelly Services, Inc.Valencia, California, US
38,00 US$–50,00 US$ por hora
Temporal
Regulatory Affairs Specialist - Valencia, CA.Kelly® Science & Clinical is seeking a Regulatory Specialist for a temporary, long-term position (approx. Valencia, CA, with occasional work in Burb...Mostrar másÚltima actualización: hace 6 días
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PRINCIPAL ANALYST, CEO - LEGISLATIVE AFFAIRS

PRINCIPAL ANALYST, CEO - LEGISLATIVE AFFAIRS

County of Los Angeles, CACA, United States
142.601,52 US$–192.186,72 US$ anual
A tiempo completo +1
When to Submit Your Application : .Applications will be accepted beginning.This examination will remain open until the needs of the service are met and is subject to closure without prior notice.No w...Mostrar másÚltima actualización: hace 2 días
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EXTERNAL AFFAIRS - ADMINISTRATIVE SPECIALIST

EXTERNAL AFFAIRS - ADMINISTRATIVE SPECIALIST

Crystal StairsCA, United States
A tiempo completo
Improving the Lives of Families through.Child Care Services, Research, and Advocacy.Excellence • Relationships • Integrity • Empowerment. External Affairs - Administrative specialist.Under general s...Mostrar másÚltima actualización: hace 9 días
Regulatory Affairs Specialist

Regulatory Affairs Specialist

Kelly ServicesSanta Clarita, CA, US
38,00 US$–50,00 US$ por hora
A tiempo completo +1
Regulatory Affairs Specialist - Valencia, CA.Kelly® Science & Clinical is seeking a Regulatory Specialist for a temporary, long-term position (approx. Valencia, CA, with occasional work in Burba...Mostrar másÚltima actualización: hace 5 días
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SENIOR DIRECTOR, CMC REGULATORY AFFAIRS

SENIOR DIRECTOR, CMC REGULATORY AFFAIRS

Kyverna TherapeuticsCA, United States
A tiempo completo
Kyverna Therapeutics is a patient-centered, clinical-stage biopharmaceutical company focused on developing cell therapies for patients suffering from autoimmune diseases. The Kyverna therapeutic pla...Mostrar másÚltima actualización: hace 2 días
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DIRECTOR / SENIOR DIRECTOR, REGULATORY AFFAIRS

DIRECTOR / SENIOR DIRECTOR, REGULATORY AFFAIRS

SolenoCA, United States
A tiempo completo
Redwood City, California, is a clinical-stage biopharmaceutical company developing novel therapeutics for the treatment of rare diseases, including Prader-Willi syndrome (PWS).At Soleno, we are dri...Mostrar másÚltima actualización: hace 1 día
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SVP, FILM BUSINESS AND LEGAL AFFAIRS

SVP, FILM BUSINESS AND LEGAL AFFAIRS

The Wonder ProjectCA, United States
225.000,00 US$–275.000,00 US$ anual
A tiempo completo
We are excited to introduce Wonder Project, a transformative new media company for the global faith and values audience.We understand the profound impact that stories have on our lives, and our pur...Mostrar másÚltima actualización: hace 2 días
Associate Director, Field Medical Affairs-Hematology (southern CA / Hawaii)

Associate Director, Field Medical Affairs-Hematology (southern CA / Hawaii)

LifelancerCalifornia, California, United States
173.500,00 US$–283.100,00 US$ anual
Teletrabajo
A tiempo completo
Quick Apply
Associate Director, Field Medical Affairs-Hematology (southern CA / Hawaii).As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific...Mostrar másÚltima actualización: hace más de 30 días
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DIRECTOR / SR. DIRECTOR, REGULATORY AFFAIRS

DIRECTOR / SR. DIRECTOR, REGULATORY AFFAIRS

BridgeBio PharmaCA, United States
A tiempo completo
About Calcilytix & BridgeBio Pharma.BridgeBio Pharma, is developing encaleret (CLTX-305), a negative allosteric modulator of the calcium-sensing receptor (CaSR) for the treatment of Autosomal Domin...Mostrar másÚltima actualización: hace 1 día
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VP MEDICAL AFFAIRS NEURO-RARE - REMOTE OPPORTUNITY

VP MEDICAL AFFAIRS NEURO-RARE - REMOTE OPPORTUNITY

LundbeckCA, United States
A tiempo completo
Do you want to join a team where the mission is meaningful, the challenges are complex, and you can directly see the results of your hard work? Lundbeck is a global biopharmaceutical company focusi...Mostrar másÚltima actualización: hace 1 día
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VP, BUSINESS & LEGAL AFFAIRS

VP, BUSINESS & LEGAL AFFAIRS

Warner Music GroupCA, United States
175.000,00 US$–230.000,00 US$ anual
A tiempo completo
At Warner Music Group, we're a global collective of music makers and music lovers, tech innovators and inspired entrepreneurs, game-changing creatives and passionate team members.Here, we know that...Mostrar másÚltima actualización: hace 1 día
Medical Director (Medical Affairs)

Medical Director (Medical Affairs)

CVS HealthCalifornia, Work At Home, US
Teletrabajo
A tiempo completo
Bring your heart to CVS Health.Every one of us at CVS Health shares a single, clear purpose : Bringing our heart to every moment of your health. This purpose guides our commitment to deliver enhanced...Mostrar másÚltima actualización: hace más de 30 días
DIRECTOR, REGULATORY AFFAIRS

DIRECTOR, REGULATORY AFFAIRS

Revolution MedicinesCA, United States
Hace 1 día
Salario
204.000,00 US$–255.000,00 US$ anual
Tipo de contrato
  • A tiempo completo
Descripción del trabajo

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

The Opportunity :

The Director of Regulatory Affairs is accountable for the delivery of regulatory strategy for designated programs at RevMed. They will support programs and drug development teams and ensure delivery of targeted, pragmatic, well-vetted, consistent and actionable regulatory advice. The Director will support policy and process development within regulatory and cross-functionally to define a consistent RevMed approach to regulatory advice and strategy. The Director must have a thorough understanding of and be highly experienced in oncology drug development, applicable regulations, and current health authority thinking, and have strong leadership and relationship-building ability.

  • Deliver sound regulatory strategy to program teams
  • Motivate, mentor and develop direct reports
  • Ensure drug development programs are fully resourced for applicable stages of development Anticipate upcoming work; ensure robust and effective regulatory strategy support.
  • Ensure regulatory strategy takes account of competitive developments, expert feedback, and that advice is aligned with company goals and objectives
  • Ensure regulatory advice, policy and decision-making is consistent across programs and that learnings from one program are fully considered in all other programs.
  • Establish highly collaborative and effective relationships with management colleagues in Clinical Research, Clinical Operations, Regulatory Affairs, Medical Writing, Quality and other functions to ensure cross-functional alignment and team effectiveness.

Required Skills, Experience and Education :

  • Degree in life sciences, pharmacy, medicine, or related fields with a minimum of 12 years in the pharmaceutical / biotech industry or relevant work experience and a minimum of 8 years in Regulatory Affairs including regulatory strategy and leadership roles.
  • Demonstrated success in leading regulatory submissions globally
  • Direct experience with oncology drug development.
  • Experienced in representing Regulatory on cross functional teams and presenting to senior management. Excellent communicator.
  • Excellent planning and organizational skills and the ability to work simultaneously on multiple projects with tight timelines.
  • Preferred Skills :

  • An advanced degree is desirable.
  • Experience with combination studies, multiple expansion cohort, basket or umbrella and master protocols highly preferred.
  • Prior NDA experience is highly preferred.
  • The base salary range for this full-time position is $204,000 to $255,000 for candidates working onsite at our headquarters in Redwood City, CA. The range displayed on each job posting is intended to be the salary for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our salary ranges are determined by role, level, and location. Individual pay is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

    Please note that base salary is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

    Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity / expression, national origin / ancestry, age, disability, marital status, medical condition, and veteran status.

    Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our CCPA Notice and Privacy Policy. For additional information, please contact [email protected].

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