141 r programming jobs at 78 companies in Oceanside, CA
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Senior Director, Head of Statistical Programming
Malvern or San Diego or United States
HybridFull Time
Uniquity Bio: Develops novel therapeutics for immune-mediated diseases.
12+ YOE12+ years statistical programming experience in biotech/pharma/CRO, leadership experience, CDISC/SDTM/ADaM expertise, expert SAS, familiarity with R/Python, experience with regulatory submissions and CRO/vendor management.
Kura OncologyNASDAQ: KURA: Develops precision small molecule medicines for cancer treatment.
10+ YOE10+ years clinical programming experience; MS (or BS with additional experience) in quantitative field; advanced SAS skills; CDISC, ICH, GCP, 21 CFR Part 11 knowledge; experience with regulatory submissions; mentoring and vendor management experience.
15+ YOERequired bachelor's in statistics/mathematics plus ~15 years pharma experience (or master's with ~12 years preferred); oncology experience; advanced SAS and CDISC knowledge; CRO oversight; FDA/ICH familiarity; strong communication.
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).
Johnson & JohnsonNYSE: JNJ: Develops and manufactures pharmaceutical drugs and medical devices.
8+ YOE3+ Mgmt8+ years in regulated project/program management; BS in Engineering/Science; PMP or equivalent preferred; experience in R&D NPD and cross-functional leadership; travel up to 10%.
Travere TherapeuticsNASDAQ: TVTX: Developing and selling therapies for rare kidney diseases.
14+ YOE7+ Mgmt14+ years clinical SAS programming experience with 7+ years leadership; Bachelor's in Statistics/CS/Math required (Master's preferred); strong SAS/SDTM/ADaM skills, submission support, vendor management, and ability to travel 10%.
Alphatec SpineNASDAQ: ATEC: Designs and manufactures surgical implants and instruments for spine surgery.
8+ YOEMinimum 8 years leading cross-functional R&D programs for software‑intensive medical products; experience with SaMD/SiMD preferred; familiarity with ISO 13485/FDA design controls; Agile; strong communication and analytical skills.
Smartsheet, Jira, Jira Product Discovery, Confluence, Microsoft Project, Azure DevOps
Johnson & JohnsonNYSE: JNJ: Provides pharmaceutical products and medical technology healthcare solutions.
8+ YOE3+ Mgmt8+ years project/program management in a regulated environment; PMP or equivalent; Bachelor's in Engineering; experience leading cross-functional teams and external partners; travel up to 10%.
IlluminaNASDAQ: ILMN: Provides genomic sequencing and array-based solutions for genetic analysis.
12+ YOEAdvanced degree preferred (MBA or PhD). 12+ years R&D portfolio/project management experience. Experience with stage-gate processes, product development across instruments/assays/regulated products/software. PMP preferred.
Johnson & JohnsonNYSE: JNJ: Global healthcare providing pharmaceuticals and medical technologies.
8+ YOEBachelors in engineering or science required; 8+ years project/program management in regulated environments (medical devices preferred); 3+ years R&D new product development; 5+ years engineering/operations; PMP preferred; ability to manage procurement and travel up to 10%.
Global New Product Process (GNPP), Project Management Methodology (PMM), Project Management Office (PMO), Quality Control (QC)
SpyGlass PharmaNASDAQ: SGP: Developing sustained drug delivery systems for chronic eye diseases.
3+ YOEBachelor's in science/engineering required; 3–6 years R&D experience in pharma/biotech/medical device supporting cross-functional projects; strong organizational, analytical, and communication skills; PMP preferred.
Cordis: Developer of interventional cardiovascular and endovascular medical devices.
8+ YOE8+ years medical device experience, program/project management background, bachelor’s in engineering, mastery of FDA design controls (21 CFR 820); PMP or advanced PM training preferred.
PhilipsEuronext Amsterdam: PHIA: Manufactures medical imaging systems and personal care appliances.
4+ YOE4+ years project/program management experience in product development, knowledge of design controls and phase-gate, ability to lead cross-functional teams in regulated environments; Smartsheet and SAFe/Agile preferred; Bachelor's/Master's in engineering/IT/business or 8+ years experience.
Manager, Clinical Data and Reporting Standards - SDTM Programming (Hybrid)
Irvine, California, United States
$110k-$209k/yrHybridFull Time
AbbVieNYSE: ABBV: Develops and sells innovative pharmaceutical and biopharmaceutical medicines.
8+ YOEMS+8 years or BS+10 years clinical research experience; SDTM and standards development experience; experience preparing SDTM/ADaM regulatory submission materials; strong communication and standards governance skills.
StrykerNYSE: SYK: Manufactures medical devices and equipment for healthcare providers.
6+ YOEBachelor’s degree in Engineering or Business; minimum 6 years PM experience; cross‑functional leadership; proficiency with PM tools; regulated industry experience.