53 associate research director jobs at 25 companies in Fallbrook, CA
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Clinical Research Associate (Site Director)
San Diego, California, United States
$160k-$210k/yrFieldFull Time
Codera: Provides end-to-end drug development services for biotechnology companies.
3+ YOEBachelor's in life science required, 3+ years site monitoring experience, FDA/ICH/GCP knowledge, CTMS/eTMF experience preferred, willing to travel 50–65%.
BDNYSE: BDX: Manufactures medical devices, surgical instruments, and pharmacy automation systems.
10+ YOE5+ MgmtSenior leadership role overseeing complex clinical studies/registries; 10+ years in clinical research/operations; 5+ years people management; regulated environment experience.
AbbVieNYSE: ABBV: Develops and sells innovative pharmaceutical and biopharmaceutical medicines.
12+ YOEBSc required with 12+ years clinical research experience (10+ with MS). Expert knowledge of CDISC standards (CDASH, SDTM, ADaM, define.xml), metadata repository experience, data standards governance, and proven regulatory submission experience.
Protein Scientist, Assistant Director or Associate Director
Carlsbad, California, United States
$144k-$196k/yrOnsiteFull Time
Ionis PharmaceuticalsNASDAQ: IONS: Discovers and develops RNA-targeted medicines for serious diseases.
5+ YOEPhD in a relevant discipline, 5+ years industry experience (Assistant Director) or 8+ years (Associate Director), deep expertise in protein engineering and recombinant protein expression/purification in microbial and mammalian systems, experience with protein fusion design and characterization, strong communication and leadership.
Travere TherapeuticsNASDAQ: TVTX: Developing and selling therapies for rare kidney diseases.
8+ YOEB.S. in Chemistry/Biochemistry or related, 8+ years analytical development/validation/transfer experience in biotech/pharma, knowledge of HPLC/GC/MS/NMR/IR/dissolution, EMs/GMP/regulatory expertise, travel 15-20%.
HPLC, GC, MS, NMR, IR, dissolution, Veeva, Quality Doc
Avenzo Therapeutics: Developing next-generation oncology therapies for cancer patients.
6+ YOEHands-on SAS statistical programmer with CDISC experience to lead programming for clinical study protocols, oversee CRO programmers, deliver SDTM/ADaM datasets and TLFs, and ensure regulatory compliance (ICH/FDA/GCP).
XencorNASDAQ: XNCR: Develops engineered antibody therapeutics for cancer and autoimmune diseases.
10+ YOEBS in life sciences required; PhD/PharmD/MS/RN preferred. Minimum 10 years pharmaceutical clinical development experience and 2 years in therapeutic area. Experience in protocol development, safety monitoring, data review, and use of EDC and analysis tools required.
Microsoft Office, Microsoft Visio, GraphPad Prism, Spotfire, Medidata RAVE, Electronic Data Capture (EDC)
Tarsus PharmaceuticalsNASDAQ: TARS: Develops and commercializes therapeutic treatments for prevalent ophthalmic diseases.
12+ YOEDoctorate required, 12 years relevant experience (including 3+ years in Medical Affairs), experience with advisory boards/congresses, strong project management, KOL engagement, Veeva preferred, Microsoft PowerPoint/Excel proficiency.
Microsoft Office Suite, Microsoft PowerPoint, Microsoft Excel, Veeva
Rapport TherapeuticsNASDAQ: RAPP: Developing precision medicines for neurological and psychiatric disorders.
10+ YOEBachelor's in life science, 10+ years pharma/biotech experience, global drug development and neurology/small-molecule experience preferred, experience with FDA neurology divisions, leadership, strong communication.
Associate Director/Director, Medical Affairs Strategy
San Diego or Redwood City
$200k-$265k/yrHybridFull Time
Soleno TherapeuticsNASDAQ: SLNO: Develops and sells treatments for rare genetic diseases.
5+ YOEAdvanced medical/scientific degree (MD/PhD/PharmD/NP/PA),5-7 years medical affairs experience in pharma/biotech, launch/orphan experience preferred, regulatory/compliance knowledge, strong communication and strategic planning skills.
Preclinical Evidence & External Partnerships Associate Director
Yokneam or Irvine
HybridFull Time
Johnson & JohnsonNYSE: JNJ: Global healthcare providing pharmaceuticals and medical technologies.
8+ YOE2+ MgmtBachelor's in biological science required; Master's/PhD preferred. 8+ years scientific experience with 2+ years people management; expertise in preclinical science, product development and regulatory submissions; cardiovascular experience preferred.
Preclinical Evidence & External Partnerships Associate Director
Yokneam or Irvine
HybridFull Time
Johnson & JohnsonNYSE: JNJ: Provides pharmaceutical products and medical technology healthcare solutions.
8+ YOE2+ MgmtBachelor's in biological science required; advanced degree preferred. 8+ years scientific experience with 2+ years people management; expertise in preclinical science, regulatory submissions, and medical device product development.
Associate Director, Functional Genomics, Data Science
Cambridge or San Diego
$176k-$277k/yrHybridFull Time
Merck & Co.NYSE: MRK: Produces prescription medicines, vaccines, and animal health products.
4+ YOEPhD in a quantitative/biological STEM field, 4+ years industry or applied academic experience, expertise in functional genomics/CRISPR, single-cell and multi-omics analysis, ML and image analysis, and strong communication skills.
Amazon Web Services (AWS), Linux, R, Python, Git, R Shiny, LLM
Acadia PharmaceuticalsNASDAQ: ACAD: Develops and sells medicines for neurological and rare diseases.
8+ YOEBachelor's in relevant field, 8+ years in analytics/AI or digital innovation within pharma/biotech/healthcare, hands-on AI-driven product and dashboard development, knowledge of CDISC and FHIR, willingness to travel domestically and internationally.
Bristol Myers SquibbNew York Stock Exchange: BMY: Develops and distributes innovative medicines for serious diseases.
8+ YOEPhD in pharmacology/cancer biology/toxicology,8+ years industry experience in in‑vivo oncology pharmacology,leadership of cross‑functional teams,IACUC/AALAC experience,knowledge of radiopharmaceuticals; AI/computational tools desirable.
Tarsus PharmaceuticalsNASDAQ: TARS: Developing therapeutics for eye care and infectious disease prevention.
12+ YOEAdvanced doctorate (OD/MD/PhD/PharmD) required; 12 years relevant experience including ≥3 years in Medical Affairs; advisory board/congress execution experience; strong project management and communication; proficiency in Microsoft Office (PowerPoint, Excel) and Veeva preferred.
Microsoft Office Suite, Microsoft PowerPoint, Microsoft Excel, Veeva
ADARx Pharmaceuticals: Develops RNA-targeting therapeutics for treating genetic and cardiometabolic diseases.
10+ YOE10+ years GCP QA experience in biotech/pharma, experience with late-stage trials and inspection readiness; bachelor's in life sciences/pharmacy required; advanced degree preferred; strong leadership and communication skills.
San Francisco or New York City or Santa Monica or Los Angeles or Palo Alto or Chicago or Washington or Boston or Colorado or Seattle or San Diego or Reston
$185k-$225k/yrOnsiteFull Time
Cooley: Provides legal counsel to technology and life sciences companies.
8+ YOE4+ Mgmt8+ years relevant marketing or business development experience with 4+ years management; bachelor's degree; professional services or B2B marketing experience; CRM, Microsoft Office, and iManage proficiency; brand research and campaign experience.