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Drug Discovery Development Jobs in California (NOW HIRING)

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Drug Discovery Development information

What is drug discovery and development?

Drug discovery and development is the process of identifying new candidate medications and bringing them to market. It involves several stages, including target identification, screening of compounds, preclinical studies, clinical trials, and regulatory approval. The goal is to find safe and effective drugs that can treat or prevent diseases. This process is complex, time-consuming, and requires collaboration among scientists, clinicians, and regulatory agencies. Successful drug development can take many years and significant financial investment.

What are some common challenges faced by professionals in drug discovery development when transitioning from early-stage research to clinical trials?

One common challenge in Drug Discovery Development is ensuring that promising compounds identified during early-stage research demonstrate both efficacy and safety in preclinical and clinical settings. This transition requires close collaboration between multidisciplinary teams, including chemists, biologists, toxicologists, and regulatory experts. Navigating regulatory requirements, securing funding, and managing timelines are also significant challenges. Professionals must be adept at adapting project strategies based on new data and feedback from regulatory agencies to keep development on track.

What are the key skills and qualifications needed to thrive in drug discovery development, and why are they important?

To thrive in Drug Discovery Development, you need a solid background in biochemistry, pharmacology, or related life sciences, typically with an advanced degree such as a PhD or MS. Proficiency in laboratory techniques, data analysis software (e.g., Prism, ChemDraw), and familiarity with regulatory standards are essential. Strong problem-solving skills, attention to detail, and effective teamwork set outstanding professionals apart in this field. These skills and qualities are critical for efficiently developing safe, effective drugs and successfully advancing compounds through the discovery pipeline.

What is the difference between Drug Discovery Development vs Drug Regulatory Affairs?

AspectDrug Discovery DevelopmentDrug Regulatory Affairs
Primary FocusIdentifying and developing new drug candidates through research and laboratory workEnsuring compliance with regulations and obtaining approvals for drugs
Work EnvironmentLaboratories, research facilities, early-stage development teamsRegulatory agencies, pharmaceutical companies, compliance departments
Required CredentialsDegree in life sciences, chemistry, or related fields; often PhDs or advanced degreesDegree in life sciences, pharmacy, or related fields; regulatory certifications beneficial

Drug Discovery Development focuses on creating new drugs through research, while Drug Regulatory Affairs ensures these drugs meet legal standards for market approval. Both roles are essential in the pharmaceutical industry but differ in their core responsibilities and work environments.

What are popular job titles related to Drug Discovery Development jobs in California?

For Drug Discovery Development jobs in California, the most frequently searched job titles are:

What job categories do people searching Drug Discovery Development jobs in California look for?

The top searched job categories for Drug Discovery Development jobs in California are:

What cities in California are hiring for Drug Discovery Development jobs?

Cities in California with the most Drug Discovery Development job openings:

Infographic showing various Drug Discovery Development job openings in California as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 16% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Scientist, Drug Discovery

Palo Alto, CA • On-site

Full-time

Re-posted 9 days ago


Job description

About Transcripta Bio
Transcripta Bio is a preclinical-stage AI drug discovery company pioneering a patient-first approach to therapeutics. Headquartered in Palo Alto, CA, we have built a proprietary closed-loop discovery engine - comprising our Disease Signature Atlas, Drug-Gene Atlas, and Conductor AI platform - that integrates single-cell patient transcriptomics, causal human genetics, and pre-validated chemistry to identify and advance drug candidates with a structural edge over conventional approaches.
We are looking for a Scientist to become a cornerstone of our drug discovery operations. You will own key areas of our experimental platform - from cell culture and high-throughput drug screening to the downstream assays that validate hits, interrogate mechanisms of action, and guide program decisions. This is a hands-on role with real scientific ownership, where your work directly powers our discovery engine.
What you'll do
• Maintain, expand, and bank disease-relevant human cell lines, including induced pluripotent stem cells (iPSCs) and iPSC-derived cell types, while ensuring consistent quality and reproducibility.
• Lead and support high-throughput small molecule drug screening campaigns utilizing automated liquid handlers and plate-based platforms. Design screening workflows, ensure data integrity, and resolve technical issues efficiently.
• Design and conduct downstream validation experiments to confirm screening hits and interrogate drug mechanisms of action, utilizing high-content imaging, qPCR, immunocytochemistry, Western blot, ELISA, and quantitative protein assays.
• Develop and optimize cell-based assays for disease-relevant biological readouts, collaborating with computational and therapeutic teams to align experimental outputs with platform requirements.
• Translate complex datasets into clear scientific narratives. Present findings at internal meetings and contribute to reports, publications, and external communications.
• Maintain detailed records in the electronic laboratory notebook (ELN) and contribute to SOPs, protocol documentation, and best practice development as the organization scales.
• Serve as a technical resource for junior team members, supporting a culture of scientific excellence.
• Support lab operations, including reagent preparation, equipment maintenance, and vendor coordination.
Qualifications
Required
• PhD in Cell Biology, Biochemistry, Molecular Biology, Pharmacology, or a closely related field with 3-5+ years of industry or postdoctoral experience; or MS with 6+ years of relevant industry experience.
• Demonstrated expertise in iPSC maintenance, differentiation, and quality assessment. Experience with primary human cells or disease-relevant iPSC-derived cell types is strongly preferred.
• Hands-on experience running or supporting high-throughput drug screening workflows, including familiarity with liquid handling automation (e.g., Hamilton, Tecan, Beckman, or equivalent).
• Relevant experience in small molecule drug discovery, including interrogating drug mechanism of action in cellular models.
• Proficiency in downstream validation techniques, including high-content imaging and analysis (e.g., Opera Phenix, ImageXpress), immunocytochemistry, Western blot, and quantitative protein assays (ELISA, MSD, or equivalent).
• Strong experimental design instincts: ability to independently scope assays, troubleshoot, and interpret data with scientific rigor and speed.
• Excellent organizational skills and high standards of documentation; comfortable working in an ELN-based environment.
• Collaborative and communicative - you thrive in cross-functional teams and can translate bench-level findings for computational colleagues and leadership alike.
• Thrives in a fast-paced, resource-constrained startup environment where adaptability and initiative are essential.
Preferred
• Experience with functional genomics approaches.
• Familiarity with transcriptomics methods (bulk or single-cell RNA-seq) or experience working with bioinformatics teams to interpret experimental data.
• Basic data analysis skills using Python, R, or similar tools.