166 Biopharmaceutical Leadership jobs in San Jose.

Redwood City

• Skills: market access, oncology, health economics, payer engagement, field input team, value proposition, healthcare payer landscape, promotional regulatory review, cross-functional collaboration, analytical activities
• Experience: 6+ years of experience in market access, pricing, health economics, or related fields within the pharmaceutical or biotechnology industry, plus oncology/hematology experience.
• Type: Full-time

Palo Alto

• Skills: Pharmacovigilance, Drug Safety, Individual Case Safety Reports (ICSRs), FDA safety regulations, ICH Guidelines, Adverse events, Study Management Teams (SMTs), Safety Management Plan (SMPs), Training documents (SOPs), Market Research and Patient Support programs (MAPs)
• Experience: Minimum of 8 years recent experience in Pharmacovigilance required; relevant pharmaceutical industry experience in drug safety required.

San Jose

• Skills: clinical content strategy, oncology pharmacy, data-driven planning, evidence-based content, clinical data tools, Python, SQL, compliance, cross-functional collaboration, patient education resources
• Experience: 4+ years of experience in a patient-facing oncology role
• Type: Full-time

South San Francisco

• Skills: client satisfaction, program coordination, cell and gene therapy, manufacturing, alliance management, communication, creative problem solving, fast-paced environment, mission-driven, multidisciplinary role
• Experience: Experienced in client relations and alliance management

South San Francisco

• Skills: Intellectual Property, IP, Attorney, small molecule, product candidates, collaboratively, inventors, senior scientific leaders, legal team, precision medicine
• Experience: Experienced
• Type: Full-time

Fremont

• Skills: clinical trials, Clinical Research Associate, GCP, FDA, ICH guidelines, monitoring, regulatory compliance, patient recruitment, medical device studies, data capture systems
• Experience: Minimum of 5 years of experience working in clinical trials with 3 years as a Clinical Research Associate
• Type: Full-time

South San Francisco

• Skills: immunology, synthetic biology, therapeutics development, functional assays, pre-clinical models, T cell biology, nucleic acid delivery technologies, pooled screening, functional genomics, aging biology
• Experience: Experience leading a team and managing direct reports; Experience with therapeutics development, ideally leading a portion of a discovery or development process in an immunology, infectious disease, or inflammatory disease setting; Deep knowledge of immunology & lymphocyte biology.

Menlo Park

• Skills: genetic medicines, mRNA, gene correction, lipid nanoparticle, targeted delivery, clinical-stage, therapeutics, disease-modifying, health insurance, career development
• Type: Full-Time

Redwood City

• Skills: Pharmacokinetics, Biomarker analyses, statistical expert, clinical program teams, clinical documents, clinical protocol, statistical analysis plan, PK modeling, biomarker analysis, CDISC standards
• Experience: 12 years of relevant experience with MS/MA degree, or 8 years with PhD in related discipline
• Type: Full-time

South San Francisco

• Skills: clinical pharmacology, drug development, data analysis, pharmacokinetics, regulatory submissions, clinical trials, translational science, quantitative pharmacology, vendor management, cross-functional collaboration
• Experience: PhD in Pharmacology and/or PharmD with at least 3+ years of industry experience in clinical pharmacology or pharmacometrics
• Type: Full-time

Redwood City

• Skills: data management, clinical studies, database activities, protocol review, data integrity, data cleaning, oncology, Medidata RAVE, regulatory guidelines, communication skills
• Experience: Minimum of 7 years of clinical data management experience in the pharmaceutical, biotechnology industry or in a CRO.
• Type: Full-time

Palo Alto

• Skills: director, assay development, lung cancer screening, collaborative teams, multidisciplinary, development lifecycle, problem-solving, scientific knowledge, team communication, innovation

South San Francisco

• Skills: CAR T-cell therapy, solid tumors, cell therapy, clinical-stage, medicines, immunology, discovery, scientist, programmable, patients

Alameda

• Skills: medical coding, clinical trials, coding strategy, vendor partnerships, ICH-GCP guidelines, clinical data management, project management, MedDRA, WHODrug, coding expertise
• Experience: 11+ years of related experience
• Type: Full-time

San Jose

• Skills: clinical research, monitoring, study management, Good Clinical Practice, site management, data integrity, regulatory submissions, recruitment, documentation, communication
• Experience: Some organizations require completion of CRA training program or prior monitoring experience.
• Type: Full time

Palo Alto

• Skills: Hematology, Oncology, clinical development, medical monitoring, regulatory interactions, clinical trial data, safety findings, strategic input, clinical protocols, external relationships
• Experience: 3+ years academic and/or pharmaceutical industry experience
• Type: Full-time

Menlo Park

• Skills: clinical data management, data integrity, clinical programs, strategic leadership, operational expertise, high-quality data solutions, decision-making, regulatory submissions

South San Francisco

• Skills: pharmacokinetics, ADME, drug candidates, biotechnology, therapeutics, preclinical, regulatory, collaborative, innovation, drug discovery
• Experience: Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable] and 3 years of directly related experience Or Master’s degree and 6 years of directly related experience Or Bachelor’s degree and 8 years of directly related experience
• Type: Full time

South San Francisco

• Skills: biostatistics, clinical development, study design, regulatory submissions, statistical analysis, SAS, R programming, clinical study protocols, vendor management, leadership
• Experience: 7+ years of experience working in early- and late-stage clinical development in the pharma/biotech industry.

Menlo Park

• Skills: data management, clinical trials, CDISC compliance, EDC systems, SOPs, data quality, project management, pharmacovigilance, biomedical data, data visualization
• Experience: 12+ years experience in clinical trial industry (med device, pharma or biotech), 10+ years experience in data management in clinical trial industry.

Oakland

• Skills: data management, clinical data management, project management, negotiations, quality management, financial tracking, process improvements, Good Clinical Practices, regulatory guidelines, compliance
• Experience: 5 years direct Data Management experience, including 3 or more years as a CDM project lead.
• Type: Full time

Sunnyvale

• Skills: clinical studies, evidence generation, clinical protocols, project management, regulatory compliance, biostatistics, clinical research, data analysis, stakeholder engagement, medical device trials
• Experience: Minimum Advanced degree in a scientific/bioengineering field (M.S., Ph.D. or M.D.) with a minimum of 5 years of experience in clinical research, or Bachelor’s degree in a scientific/bioengineering field with a minimum of 8 years of experience in clinical research is preferred, or a minimum of 10 years of experience in clinical research with relevant training.
• Type: Clinical & Medical Affairs

Hayward

• Skills: clinical effectiveness, multidisciplinary team, community health, supervising clinicians, clinical quality, patient-centered care, administrative responsibilities, educational programming, health assessments, leadership
• Experience: Minimum five (5) years of clinical experience required and minimum two (2) years of experience supervising providers
• Type: Full-time

Sunnyvale

• Skills: clinical research, regulatory approvals, study design, clinical protocols, evidence generation, biostatistics, clinical trials, GCP, project management, clinical outcomes
• Experience: Minimum of 2-3 years of experience in clinical research for advanced degree; 5 years for Bachelor's degree.

Santa Clara

• Skills: Medical Affairs, Flexible Robotics, Robotic Bronchoscopy, Clinical Research, Regulatory Compliance, Stakeholder Engagement, Strategic Leadership, Medical Safety, Quality Assurance, Patient Safety
• Experience: Minimum of 7+ years relevant experience in post-graduate medical education including specialty residency, fellowship or subspecialty training, clinical practice, dedicated research, or other related training/experience in Interventional Pulmonology required. 2+ years flexible robotics experience is required.
• Type: Fully Onsite

Fremont

• Skills: clinical trials, clinical studies, Good Clinical Practice, compliance, medical devices, ISO14155, communication, project management, neuroscience, regulatory requirements
• Experience: 5+ years of academic or industry experience working with medical devices
• Type: Full-time

South San Francisco

• Skills: pharmacokinetics, drug metabolism, DMPK, clinical pharmacology, preclinical studies, biologics, small molecules, machine learning, ADME, clinical trial design
• Experience: 10+ years of experience in PK/DM in biotechnology and/or pharmaceutical industries
• Type: Full-time

Santa Clara

• Skills: clinical support, interventional procedures, medical devices, clinical studies, training materials, data collection, hospital systems, customer relations, life sciences, product knowledge
• Experience: Minimum 2 years’ experience directly supporting interventional or surgical procedures within a hospital setting OR, 1 year of industry, hospital-based life sciences, sales support experience.
• Type: Fully Remote

San Jose

• Skills: Regulatory Affairs, Consulting, Medical Device, Senior Regulatory Affairs Consultant, Senior Regulatory Affairs Associate, Labeling Operations, Regulatory Lead, Functional Service Provider, Remote, Clinical Regulatory Affairs

Palo Alto

• Skills: Statistical Programming, CDISC SDTM, ADaM datasets, Clinical Trials, SAS programming, Data Analysis, Regulatory Submission, Clinical Study Reports, Data Integrity, Stakeholder Collaboration
• Experience: At least 10 years in pharmaceutical or bio-pharmaceutical industry with a bachelor’s degree in statistics, mathematics or equivalent, or at least 7 years with a master's degree.

South San Francisco

• Skills: Strategic Planning, Operational Effectiveness, Performance Management, Continuous Improvement, Stakeholder Engagement, Project Management, Risk Management, Drug Development, Communications, Leadership
• Experience: 4+ years of Scientific and/or Operations and/or Business experience or 7 years with a Master's degree or 9 years with a Bachelor's degree in a related field.
• Type: Full-time

Palo Alto

• Skills: patient marketing, strategic input, education programs, promotional marketing, cross-functional collaboration, market research, execution management, KPI tracking, regulatory compliance, patient advocacy
• Experience: 5+ years of industry experience, including 2 years in pharmaceutical marketing
• Type: Full-time

Millbrae

• Skills: Computational Biology, Drug Discovery, Bioinformatics, Data Strategy, Biomarker Development, Team Leadership, Machine Learning, High Dimensional Analysis, Scientific Methodologies, Collaborative Research
• Experience: 12+ years with a Post Graduate degree or 15+ years with a Bachelor’s degree in a related field
• Type: Full-time

Oakland

• Skills: Clinical Trial Design, Clinical Trials, Phase I, Phase II, Medical Monitoring, Safety Oversight, Regulatory Requirements, Compliance, Clinical Strategy, Cross-functional Team
• Experience: A minimum of 6 years of industry experience in clinical development in a pharmaceutical or biotech company setting.
• Type: Full-time

Palo Alto

• Skills: pharmaceutical integrations, technical engagement, regulatory compliance, clinical trial management, drug safety monitoring, patient engagement, EHR, data integrations, healthcare standards, client relationships
• Experience: 5+ years of experience in healthcare or pharmaceutical implementation, product management, or technical solutions roles.
• Type: Full time

San Carlos

• Skills: Medical Science Liaison, Oncology, Hematological Cancer, KOLs, Clinical Trials, Scientific Presentations, Healthcare Providers, Scientific Resource, Stakeholder Engagement, Research Initiatives
• Experience: Health care professionals with relevant scientific knowledge and/or clinical training in hematologic oncology will be considered.
• Type: Remote

South San Francisco

• Skills: Medical Director, Rheumatology, Clinical Development, SLE program, TYK-2 inhibitor, Phase 2b study, Sponsor medical monitor, CRO collaboration, Data Monitoring Committee, Pharmacovigilance
• Experience: Licensed physician; Board certification in rheumatology or related field (desired); Industry experience in pharmacovigilance or clinical development (helpful).

Newark

• Skills: leadership, transformation management, clinical quality, strategic planning, collaboration, communication, healthcare management, teamwork, quality management, clinical compliance
• Experience: 5 years of health care management experience; 10 years of clinical practice

South San Francisco

• Skills: Toxicology, Bioanalytical, Nonclinical evaluations, Drug discovery, Pharma, Clinical trials, Regulatory, Leadership, Collaboration, Critical thinking
• Experience: 15+ years of post-training experience in academia, biotech or pharma.
• Type: Full-time

South San Francisco

• Skills: contracts management, negotiation, research agreements, life sciences, legal issues, Master Service Agreements, License Agreements, Consulting Agreements, contract workflow, stakeholder management
• Experience: 5+ years in the life sciences industry
• Type: Full-time

Palo Alto

• Skills: compliance, legal counsel, healthcare, contract management, regulatory requirements, diagnostic, risk mitigation, clinical laboratories, commercial agreements, healthcare professionals

South San Francisco

• Skills: endothelial biology, functional assays, pre-clinical models, mRNA reprogramming, nucleic acid delivery, experimental data, drug development, mouse models, single cell genomics, CRISPR fitness screens
• Experience: 5+ years

Palo Alto

• Skills: Regulatory Affairs, BLA, NDA, clinical trials, strategic leadership, collaboration, pharmaceutical, biotechnology, lifecycle management, FDA
• Experience: Minimum 12 years of documented professional experience at a Regulatory Affairs leadership position within the pharmaceutical or biotechnology industry.

Santa Clara

• Skills: Regulatory Compliance, Healthcare Innovation, Biomedical Technology, Intravascular Lithotripsy, Cardiovascular Disease, Compliance Strategies, Quality Assurance, Inspection Management, Risk Management, Cross-Functional Collaboration
• Type: Full-time

San Jose

• Skills: Biotechnology, Clinical Trials, Project Leadership, Kidney Transplant, Patient Care, Drug Development, Regulatory Affairs, Data Management, Clinical Operations, Statistical Programming
• Type: Remote

Palo Alto

• Skills: clinical data, measurement science, data engineering, analytics, clinical studies, diagnostic products, machine learning, software engineering, fragmentomics, health outcomes

South San Francisco

• Skills: CMC, regulatory documentation, clinical trials, drug substance, drug products, GMP, risk management, vendor management, quality systems, analytical activities
• Experience: 10+ years in industry CMC; 3+ years of experience as CMC team leader.
• Type: Full-time

San Mateo

• Skills: regulatory strategy, FDA compliance, medical devices, global regulations, submissions, clinical studies, quality management systems, risk management, inspections, team management
• Experience: 7+ years in regulatory affairs for medical devices
• Type: Hybrid

Livermore

• Skills: cell biology, cardiac focus, cellular models, toxicology, electrocardiography, in vivo assessments, research projects, data sets, scientist collaboration, technical reports
• Type: Full-time

Palo Alto

• Skills: biostatistics, drug development, clinical study design, statistical analysis plans, exploratory analysis, FDA regulations, SAS programming, data analysis, cross-functional collaboration, clinical study reports
• Experience: PhD in statistics or equivalent, with at least 10 years of relevant experience in biotechnology or pharmaceutical industry
• Type: Full-time

San Carlos

• Skills: oncology, product management, innovation, diagnostics, genomic profiling, research, market analysis, product development, business plans, cross-functional collaboration
• Experience: Minimum of 5 years of product management with at least (10+) years overall experience in product management, product development, marketing and/or strategy.
• Type: Full-time

Palo Alto

• Skills: DMPK, ADME, PK/PD, biopharmaceutical, genetic diseases, drug development, clinical development, pharmacokinetics, small molecules, lead optimization
• Experience: 10–15+ years’ industry experience in small-molecule DMPK, with at least five years in a leadership or project-team representative role
• Type: Full-time

South San Francisco

• Skills: antibody discovery, in vitro display technologies, phage display, ribosome display, yeast display, team management, biopharma programs, molecular biology, antibody engineering, scientific databases
• Experience: PhD or equivalent in Biochemistry, Molecular Biology, Protein Engineering or related field; MS / MA with 3-5 years industry experience.
• Type: Full-time