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Clinical Science Jobs (NOW HIRING)

Director, Clinical Science

South San Francisco, CA ยท On-site

$96K - $131K/yr

IDEAYA Biosciences is seeking a South San Francisco based experienced, motivated, outgoing Clinical Scientist. Reporting to the Sr. Medical Director, Late-Stage Clinical Development, the Director ...

Clinical Science & Data Interpretation * Analyze and interpret emerging clinical, safety, efficacy, and biomarker data to support study conduct and decision-making. * Support data cleaning efforts ...

Clinical Science & Data Interpretation * Analyze and interpret emerging clinical, safety, efficacy, and biomarker data to support study conduct and decision-making. * Support data cleaning efforts ...

Clinical Science & Data Interpretation * Analyze and interpret emerging clinical, safety, efficacy, and biomarker data to support study conduct and decision-making. * Support data cleaning efforts ...

Director, Clinical Science

Livermore, CA ยท Hybrid

$204K - $327K/yr

This position will function as director in charge of all required clinical science, new test development, validations, and overall clinical quality of the assigned department(s). This position may be ...

Director, Clinical Science

Livermore, CA ยท On-site

$204K - $327K/yr

This position will function as director in charge of all required clinical science, new test development, validations, and overall clinical quality of the assigned department(s). This position may be ...

The successful candidate will bring strong clinical science expertise and experience supporting studies with sites across both the United States and Asia-Pacific (APAC) regions. As part of a lean and ...

About The Role We are seeking a rigorous and strategic Clinical Science Lead to serve as the scientific backbone of Neverstop - a mission-driven wellness platform helping people age well. We take a ...

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Clinical Science information

See salary details

$27.5K

$121.3K

$236.5K

How much do clinical science jobs pay per year?

As of Jul 10, 2026, the average yearly pay for clinical science in the United States is $121,346.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $181,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Scientist, and why are they important?

To thrive as a Clinical Scientist, you need a solid grounding in biological or biomedical sciences, often supported by an advanced degree such as an MSc or PhD, along with relevant clinical laboratory experience. Familiarity with laboratory information management systems (LIMS), specialized diagnostic equipment, and certifications like HCPC registration (in the UK) are typically required. Analytical thinking, attention to detail, and effective communication are crucial soft skills for interpreting results and collaborating with healthcare teams. These competencies ensure accurate diagnostics, patient safety, and the advancement of medical research and treatments.

What are some common challenges faced by professionals in Clinical Science roles, and how can they be addressed?

Professionals in Clinical Science often encounter challenges such as managing complex clinical trial protocols, ensuring regulatory compliance, and coordinating effectively with cross-functional teams. Navigating changing study requirements and tight timelines can also be demanding. To address these challenges, it's important to stay organized, maintain up-to-date knowledge of regulatory guidelines, and foster strong communication with colleagues in clinical operations, data management, and regulatory affairs. Leveraging project management tools and proactively seeking clarification on study objectives can also help Clinical Scientists succeed in their roles.

What is the difference between Clinical Science vs Clinical Research Coordinator?

AspectClinical ScienceClinical Research Coordinator
Required CredentialsBachelor's or higher in life sciences, certifications like CCRP or CCRA often preferredBachelor's degree in health sciences or related field, often with certification like CCRP
Work EnvironmentPharmaceutical companies, biotech firms, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry and academia for drug development and clinical trialsPrimarily in clinical trial sites managing patient data and study logistics

Clinical Science professionals focus on designing, analyzing, and overseeing clinical trials, often working in labs or industry settings. Clinical Research Coordinators manage day-to-day trial operations at research sites, ensuring protocol adherence and patient safety. Both roles require similar credentials but differ in responsibilities and work environments.

What is clinical science?

Clinical science is a field of study that focuses on research and practices related to human health and disease, particularly as they apply to patient care. It involves the investigation of the causes, development, diagnosis, and treatment of illnesses through laboratory research, clinical trials, and patient-focused studies. Professionals in clinical science often work in hospitals, research institutions, or pharmaceutical companies, contributing to advances in medical knowledge and healthcare. The field bridges the gap between laboratory research and clinical practice, ensuring that scientific discoveries lead to improved patient outcomes.
More about Clinical Science jobs
What cities are hiring for Clinical Science jobs? Cities with the most Clinical Science job openings:
What are the most commonly searched types of Clinical Science jobs? The most popular types of Clinical Science jobs are:
What states have the most Clinical Science jobs? States with the most job openings for Clinical Science jobs include:
Infographic showing various Clinical Science job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $121,346 per year, or $58.3 per hour.

Director, Clinical Science

Ideayabio

South San Francisco, CA โ€ข On-site

$96K - $131K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 18 days ago


Job description

Non-Solicitation Policy and Notice to Agencies and Recruiters:

IDEAYA's Non-Solicitation Policy strictly prohibits agencies and recruiters from any contact and communication with IDEAYA employees, managers, and leaders to submit unsolicited candidate resumes and/or to solicit business partnerships. Submission of unsolicited candidate resumes by agencies or recruiters with or without a contract in place with IDEAYA Biosciences Inc. will not create any implied obligation. Failure to comply with this policy will result in disqualification from current and future business opportunities with IDEAYA Biosciences. All recruiting and talent agency decisions are strictly managed by the internal IDEAYA Human Resources function. All communication by external agencies and recruiters must be directed to humanresources@ideayabio.com. We ask that you only email your interest once.

Job Summary

About IDEAYA Biosciences:
IDEAYA is a precision medicine oncology company committed to the discovery, development, and commercialization of transformative therapies for cancer. Our approach integrates expertise in small-molecule drug discovery, structural biology and bioinformatics with robust internal capabilities in identifying and validating translational biomarkers to develop tailored, potentially first-in-class targeted therapies aligned to the genetic drivers of disease. We have built a deep pipeline of product candidates focused on synthetic lethality and antibody-drug conjugates, or ADCs, for molecularly defined solid tumor indications. Our mission is to bring forth the next wave of precision oncology therapies that are more selective, more effective, and deeply personalized with the goal of altering the course of disease and improving clinical outcomes for patients with cancer.
When you're at IDEAYA, you will be in the midst of brilliant minds working on precision medicine therapies to help cancer patients. We are passionate and committed about being on the forefront of oncology medicine, which means we all have a high internal drive that is at the very core of every person at IDEAYA. We are inquisitive, ask deep questions, and are data-driven innovators who like to collaborate and use team work to move science forward. For more information, please see www.ideayabio.com.
Location: South San Francisco, CA
Position Summary:
IDEAYA Biosciences is seeking a South San Francisco based experienced, motivated, outgoing Clinical Scientist. Reporting to the Sr. Medical Director, Late-Stage Clinical Development, the Director will work closely with the clinical leader providing medical and -scientific expertise to one or more clinical projects.
This position is based in our South San Francisco headquarter office and required to be onsite four days per week per our company policy.
Reporting to: Senior Medical Director, Late-Stage Clinical Development

Job Description

What you'll do:

Typical activities may include but will not necessarily be limited to:

  • With the medical monitor (MM), writing clinical development concepts and plans for molecules at all stages of development
  • With the medical monitor, writing initial and or later drafts of protocol synopses, protocols and protocol amendments
  • Reviewing informed consent forms and reviewing/adjudicating site-specific ICF requests
  • Partnering with the MM and Clinical Operations on site selection, start-up and communication activities
  • With the medical monitor writing or updating clinical sections of investigator brochures
  • Reviewing clinical/safety sections of NDAs/MAAs
  • Serving as a member of the clinical sub team
  • Reviewing and interpreting data listings including safety data and serious adverse events
  • Assisting the MM as an author of clinical study reports and associated publications
  • Creating clinical study- or program-related slide decks for internal and external use
  • Training of colleagues, CRO and study site staff on the therapeutic area, molecule and protocols as appropriate
  • With the MM organizing and participating in opinion leader advisory boards
  • Contributing to or performing therapeutic area/indication research and competitor analysis
  • With the MM support Health Authority (HA) interaction, accountable for providing responses to HA inspection observations and internal audits

Requirements:

  • Bachelor's degree and strong knowledge of clinical oncology gained through previous clinical development experience are required.
  • Postgraduate qualification in clinical oncology (e.g., master's degree) would be welcomed as would MD, Nurse Practitioner's License, PharmD or PhD
  • At least 2 years of industry experience in oncology
  • Previous participation in a clinical development program is essential, preferably involvement in all stages of clinical trials (i.e., from start up to study report)
  • Skilled in protocol design, interpretation, and data cleaning.
  • Experience in assessment of adverse events and safety of patients participating in therapeutic clinical trials is preferred
  • Knowledge of Good Clinical Practice
  • Excellent written and oral communication
  • Capacity to adapt to a fast-paced and changing environment
  • Fluency in English is required.

Personal Qualities:

The successful candidate will be a confident person keen to take responsibility for assigned activities. Although working under the guidance of a manager and the clinical leader of the program, the Director will be expected to function independently and would thrive in a mentored rather than a directed environment.

The Director will feel comfortable presenting data to peers, investigators and senior management/executive committee. They will be able to embrace the challenges and opportunities offered in a small company environment and to capitalize on the experience.

All employees are expected to act with integrity and in full compliance with applicable laws, regulations, and IDEAYA policies, including IDEAYA's Code of Conduct.
Employees must demonstrate good judgement and ethical behavior in all business activities, maintain patient and product safety as a top priority, and report any suspected violations of law or Company policy through appropriate channels

Total Rewards

Along with our inspiring mission, and highly collaborative and inclusive environment, IDEAYA offers a competitive total rewards package that reflects our pay-for-performance philosophy where employees are eligible to be considered for merit-based salary increases, company discretionary short-term incentive plan participation, and company discretionary stock option awards (based on board approval). Our comprehensive benefits package includes, but is not limited to, medical/dental/vision coverage (100% company paid for employees and 90% company paid for dependents), 401k, ESPP, and wellness programs.

The expected salary range for the roleof Director, Clinical Science is $227,000-280,000. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the office location where this open position is located, the final candidates' experience within their profession, experience in the disease areas we are striving to make an impact in as a company, length of time within the industry, educational background, and performance during the interview process.

The Company complies with all laws respecting equal employment opportunities and does not discriminate against applicants with regard to any protected characteristic as defined by federal, state, and local law. This position requires you to work onsite in the office at the Company's facilities for training & meetings, with work-from-home flexibility, and the Company requires that all employees working in its facilities be fully vaccinated (except as required by applicable law). Therefore, this position requires you to be fully vaccinated from COVID-19, subject to reasonable accommodations for medical or religious reasons, and/or as otherwise required by applicable law. The Company considers you fully vaccinated once 14 days have passed since you received either the second dose in a two-dose COVID-19 vaccine series or a single-dose COVID-19 vaccine. The vaccine must have been FDA approved, have emergency use authorization from the FDA, or, for persons fully vaccinated outside of the U.S., be listed for emergency use by the World Health Organization.

IDEAYA is an equal opportunity employer. In accordance with applicable law, IDEAYA does not discriminate in hiring or otherwise in employment based on race, color, religion, sex, national origin, age, marital or veteran status, disability, sexual orientation, or any other legally protected status. EOE/AA/Vets.

We are committed to providing reasonable accommodations to qualified individuals with disabilities. If you need assistance or an accommodation due to a disability, please get in touch with us at hr@ideayabio.com.