1

Research Associate Biotech Jobs in San Ramon, CA

About NewLimit NewLimit is a biotechnology company working to radically extend human healthspan. We ... Position NewLimit is seeking an Senior/Research Associate with experience in discovery biology to ...

About NewLimit NewLimit is a biotechnology company working to radically extend human healthspan. We ... Position NewLimit is seeking an Senior/Research Associate with experience in discovery biology to ...

IndustriesStaffing and Recruiting and Biotechnology Research Referrals increase your chances of ... Fremont, CA $115,000.00-$135,000.00 2 weeks ago Research Associate, Analytical Development III ...

About the Role We are looking for a highly hands-on Research Associate to join our team and support ... A., or MS in Biology, Biochemistry, Biotechnology, or a related scientific discipline * 2-4 years ...

next page

Showing results 1-20

Research Associate Biotech information

See San Ramon, CA salary details

$18

$36

$52

How much do research associate biotech jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for research associate biotech in San Ramon, CA is $36.37, according to ZipRecruiter salary data. Most workers in this role earn between $29.28 and $41.35 per hour, depending on experience, location, and employer.

What is a Research Associate Biotech job?

A Research Associate in Biotechnology is responsible for conducting experiments, analyzing data, and supporting scientific research in areas such as pharmaceuticals, genetics, and molecular biology. They work in laboratories, using advanced equipment and techniques to develop new products, improve existing processes, or contribute to scientific discoveries. Typical tasks include preparing samples, running assays, documenting results, and collaborating with scientists and engineers. This role requires a strong background in biology, chemistry, or a related field, along with attention to detail and problem-solving skills.

What are the typical daily responsibilities of a Research Associate in Biotech?

As a Research Associate in Biotech, your daily responsibilities often include conducting laboratory experiments, preparing and analyzing samples, recording and interpreting data, and maintaining detailed lab notebooks. You may also be responsible for ensuring the smooth operation of laboratory equipment and adhering to strict safety and quality protocols. Collaboration is common, so you’ll regularly interact with scientists, lab managers, and other team members to discuss findings or help design new experiments. This role offers variety and the chance to actively contribute to innovative research projects that could advance new biotechnological solutions.

What are the key skills and qualifications needed to thrive in the Research Associate Biotech position, and why are they important?

To thrive as a Research Associate in Biotech, you need a solid background in molecular biology, biochemistry, or a related field—typically supported by a bachelor's or master’s degree. Experience with laboratory techniques such as PCR, cell culture, and analytical instrumentation, as well as familiarity with data analysis software and laboratory information management systems, is often required. Strong attention to detail, problem-solving abilities, and effective teamwork and communication skills set candidates apart. These competencies are crucial for ensuring high-quality research results, maintaining lab safety, and driving successful collaboration within scientific teams.

What job categories do people searching Research Associate Biotech jobs in San Ramon, CA look for? The top searched job categories for Research Associate Biotech jobs in San Ramon, CA are:
What cities near San Ramon, CA are hiring for Research Associate Biotech jobs? Cities near San Ramon, CA with the most Research Associate Biotech job openings:
Infographic showing various Research Associate Biotech job openings in San Ramon, CA as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $75,640 per year, or $36.4 per hour.

Senior Clinical Research Associate

Epicrispr Biotechnologies

South San Francisco, CA • On-site

$115K - $121K/yr

Full-time

Re-posted 9 days ago


Job description

Who Are We?
Our company is based on the science of our founder, Stanley Qi, one of the original CRISPR co-inventors who then furthered the technology so that DNA does not need to be cut to accomplish gene regulation. Instead, we regulate the epigenome to suppress and activate multiple genes simultaneously. We are further evolving the platform and leveraging its strengths to address unmet medical needs.
We are looking for exceptional team members who want an active role in building a rapidly growing biotech.
Position: Senior Clinical Research Associate
Location: South San Francisco, CA
Opportunity:
Epicrispr Bio is seeking a detail-oriented and proactive Senior Clinical Research Associate (CRA) to support the execution and oversight of clinical trials. This role will play a key part in ensuring studies are conducted in compliance with regulatory requirements, GCP guidelines, and company protocols, while maintaining the highest standards of quality and data integrity.
The ideal candidate will bring a strong foundation in clinical operations, experience working cross-functionally with CROs and clinical teams, and the ability to independently manage site activities while contributing to process improvements in a fast-paced, growing environment. This is an opportunity to have meaningful impact on clinical development programs while helping to build and scale operational excellence within the organization.
Roles and Responsibilities:
  • Assist the Clinical Operations team with on-site sample operations, including sample receipt, registration, and shipments in a GCP environment.
  • Support clinical trial manager with site management, including: site startup activities, co-monitoring visits alongside CRO, reviewing monitoring visit reports, coordinating vendor trainings, reviewing study newsletters, and other duties as needed, in alignment with study priorities and CTM guidance.
  • Assist clinical trial manager with data verification and ICF reviews as needed, alongside CRO, to support data quality and protocol compliance.
  • Partner with CTM and clinical team to help identify areas to improve our processes, with priorities defined by the CTM, and support implementation of agreed-upon improvements.
  • Identify and communicate site-level issues, protocol deviations, and operational risks to the CTM to support timely resolution.
  • Maintain study trackers, logs, and documentation across regulatory, site, data, and sample operations to support study oversight and execution.

Qualifications:
  • Bachelor's degree in life sciences or related field preferred
  • 2 - 5+ years of CRA or clinical research experience (biotech, pharma, or CRO environment)
  • Strong understanding of GCP, ICH guidelines, and clinical trial processes
  • Experience working with CROs and managing clinical sites
  • Excellent organizational, communication, and problem-solving skills
  • Ability to manage multiple priorities in a fast-paced environment

Compensation: The salary range for this position is $115,000 to $121,000 USD annually. This salary range is an estimate, and the actual salary may vary based on various factors, including, without limitation, individual education, experience, tenure, skills, and abilities, as well as internal equity and alignment with market data, including potential adjustments for geographic location.
Epicrispr Biotechnologies is an early-stage biotechnology company developing a novel technology platform that can provide safe and persistent control of targeted gene regulation. Our proprietary platform represents an entirely new class of therapeutics that can be leveraged to treat severe disease across numerous therapeutic areas, including complex diseases impacted by multiple genes.
Epicrispr Biotechnologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.