Senior Associate Director, Multiple Myeloma Medical Affairs
Kite Pharma
Location: San Francisco, California, United StatesCompany: KITE PHARMA, INC.Posted: 2026-10-12Kite Pharma seeks an Associate Director for Multiple Myeloma to advance US Medical Affairs strategy and execution in a dynamic oncology landscape. You will drive evidence generation, scientific exchange, and launch readiness across cross-functional teams including Field Medical, Commercial, Market Access, HEOR/RWE, Clinical Development, and Global Medical Affairs.Reporting to the U.S. MM Medical Lead, you will shape advisory boards, publications, and congress planning while managing complex#J-18808-Ljbffr
$195.67k - $253.22k
...help shape where our business and medical science goes next.We believe... ...arisen to join the U.S. Medical Affairs Team with a focus on Multiple Myeloma. In this role, you will contribute... ...U.S. Medical Affairs team as an Associate Director, Multiple Myeloma. This role will...MedicalLocal area$176.1k - $287.3k
Build our future together:As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific... ...understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. This position...MedicalFull timeRemote workWorldwideNight shiftWeekend work- ....Posted: 2026-09-30Kite Pharma, Inc. is seeking an Associate Director for the U.S. Lymphoma Medical Affairs team.This role leads strategic medical planning, collaborates... ...boards, and cross-functional leadership across multiple sites in the U.S. with travel as needed.#J-18808-...Medical
- ...shape where our business and medical science goes next. We... ...arisen to join the U.S. Medical Affairs Team with a focus on Lymphoma... ...Medical Affairs team as an Associate Director, to support our lymphoma franchise... ...cross-functionally with multiple stakeholders including: Field...MedicalLocal area
$218.06k - $327.09k
Job Title: Senior Director, Oncology Cell and Gene Therapy... ...significant unmet need in multiple myeloma and beyond.You will... ...Represent Regulatory Affairs on Global Product... ...compliance activities associated with marketed brands.... ...health benefits including medical, prescription drug,...SeniorMedicalHourly payFull timeTemporary workWorldwideFlexible hours3 days per week$187.8k - $208.6k
...functional teams, with room at the Associate Director level to own strategy and mentor... ...Description The Opportunity Report to the Senior Director, Regulatory Affairs CMC (Head of Regulatory CMC, Small... ...writing skills Ability to manage multiple projects and competing timelines...SeniorLocal area$176.1k - $287.3k
...use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Field Medical Affairs responsible for engaging in the exchange of scientific data and other medical and/or scientific information with key...MedicalFull timeRemote workWorldwideNight shift- ...AbbVie seeks a field-based medical science liaison to serve as the primary scientific... ...and supporting research initiatives in multiple myeloma. Responsibilities Identify and maintain... ...~3+ years relevant experience for Senior MSL; 0-2 years for MSL level ~ Proficiency...SeniorMedicalRelocation
- ...Nurix Therapeutics seeks a senior-level publications and medical information professional to manage clinical publication strategy, medical inquiry responses... ...requires cross-functional collaboration across medical affairs, publications, and data review initiatives....SeniorMedicalContract work
$187.8k - $208.6k
...Nurix Therapeutics seeks a Senior Manager or Associate Director to lead CMC regulatory strategy for small molecule programs from clinical development... ...related life sciences field ~ Minimum 6+ years regulatory affairs experience with substantial CMC focus ~10+ years total...Senior- ...Senior Manager/Associate Director position leading regulatory strategy for hematology-oncology programs at a clinical-stage biotech company. Responsible... ..., pharmacy, or related field ~10+ years regulatory affairs experience in pharmaceutical development ~ Demonstrated...Senior
- ...Nurix Therapeutics, Inc. is seeking a Vice President, Medical Affairs, Hematology-Oncology to build and lead a best-in-class Medical Affairs organization as the company transitions from clinical-stage to commercialization. The role entails medical strategy, field medical...SeniorMedical
$180k - $241k
...Primary Function: The Associate Director, Regulatory Affairs supports the development... ...role works closely with senior regulatory leadership to... ...Nonclinical, Biometrics, Medical Writing, CMC, and other functions... ...may vary depending on multiple individualized factors,...MedicalRemote workWorldwideRelocation package- ...maintaining strategic relationships with Multiple Myeloma thought leaders and oncology... ...objectives while partnering across commercial, medical, and compliance functions. Responsibilities... ...with marketing, sales, medical affairs, and field teams to align on expert engagement...Medical
$185k - $205k
...monotherapy data from this program across multiple solid tumor types, are advancing... ...what’s beyond. About the Role >>> Associate Director, Global Regulatory Affairs, Compliance and Project Management... ...management reporting to the Senior Director, Global Regulatory Strategy...Work at officeFlexible hours$117.2k - $260.1k
...Security Partner professionals spanning multiple levels to work directly with leadership within... ...the Security Partner career path: from Senior Analysts building foundational... ...live well including: time off programs, medical, dental, vision, mental health support, paid...SeniorMedicalFull timeRemote work- ...Francisco, California, United StatesCompany: Rigel PharmaceuticalsPosted: 2026-10-05Rigel Pharmaceuticals, Inc. is seeking an Associate Director of Medical Communications and Publications to lead strategic publication planning and publication execution across indications. You...SeniorMedical
$250k - $285k
...Regulatory Affairs Leader Headquarters Location: Emeryville, CA... ...therapeutic candidates across multiple treatment modalities... ...activities. Serve as the senior regulatory representative on... ...identity or expression, pregnancy, medical condition related to pregnancy...SeniorMedical$219k - $253k
...contracts attorney to serve as Associate Director, Contracts Counsel. Reporting to the Senior Director, Contracts, this role... ...Access, Marketing, Sales, Medical Affairs, Patient Support, Finance, Procurement... ..., with the ability to manage multiple priorities in a fast-paced...MedicalFull timeContract workLocal areaWorldwide$229.5k - $255.87k
...Associate Director Pharmacovigilance Operations Nurix Therapeutics is a... ...Data Management and Regulatory Affairs. The role also provides... ...Management Regulatory Affairs and Medical Safety to ensure alignment... ...skills; able to manage multiple products/priorities simultaneously...MedicalFull timeTemporary work- ...Job Description Job Description Job Title: Senior Medical Director, Medical Affairs Position Type: Full Time Location: Thousand Oaks, CA or San Francisco Bay Area Company Description: Latigo Biotherapeutics, Inc. is a biotechnology company focused...SeniorMedicalFull time
- ...issues today and address the medical challenges of tomorrow. We strive... ...Job Description The MSL/Senior MSL: A field based... ...Clinical Operations, and Medical Affairs Departments and physician-initiated... ..., PhD, APP (i.e.: Physician Associate or Nurse Practitioner) in a...SeniorMedicalFull timeLive inLocal areaRelocation
- ...serious health issues today and address the medical challenges of tomorrow. We strive to... .... Job Description The Medical Affairs organization provides patients,... ...the patient’s journey. The Scientific Director / Senior Medical Director, Medical Affairs - Global...SeniorMedicalWork at officeLocal area
- ...The Associate Director Regulatory Affairs US Advertising and Promotion-Oncology is responsible for setting... ...effective communication channels with key Medical Marketing Regulatory Legal and... ...recognition of when to consult departmental senior concerning absence of Director is...MedicalFull timeWork at officeLocal areaRemote work
$120.2k - $223.2k
The PositionCommercial Regulatory Affairs (CORA) is part of the Global Product and Access Legal (GPAL) organization... ...Head of GPAL in the Global Legal Pharma Department.Associate Program Directors of Commercial Medical Legal Regulatory Review Committees (CMLRs) provide regulatory...MedicalFull timeWork experience placementLocal areaWorldwideRelocation package- A small, commercial stage medical device company in the SF Bay area is seeking a Regulatory Affairs Manager or Director to lead a critical 510(k) FDA submission. The company is developing innovative surgical devices to detect gastrointestinal diseases. This role’s primary...SeniorMedical
- ...issues today and address the medical challenges of tomorrow. We... ...regulatory requirements for multiple functions. Generates new PK/... ...the below qualifications: Associate Director, Clinical Pharmacology PhD... ...delegated to by others Senior Clinical Pharmacologist:...SeniorMedicalLocal area
$176.1k - $287.3k
...Regeneron seeks an Associate Director of Field Medical Affairs specializing in cutaneous oncology for California, Nevada, and Hawaii. The role involves building relationships with key opinion leaders, providing clinical expertise to healthcare providers, and supporting...Medical$176.1k - $287.3k
...Regeneron seeks an Associate Director of Field Medical Affairs to engage with healthcare leaders and researchers in hematologic malignancies across northern California and Nevada. The role involves building scientific relationships, supporting clinical trials, and serving...Medical- ...An innovative, venture-backed medical technology company in San Francisco is seeking a Principal Regulatory Affairs Specialist to join its growing regulatory organization... ...development teams. ~ Comfortable managing multiple regulatory workstreams, timelines, and stakeholders...MedicalFull time
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