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Study Director Jobs in California (NOW HIRING)

Glaukos

Manager Study Start-up

San Clemente, CA · On-site

Prior experience providing daytoday leadership, guidance, or oversight to study teams, vendors, or functional partners; people management responsibility may be direct or matrixed. * Strong working ...

Glaukos

Manager Study Start-up

San Clemente, CA · On-site

Prior experience providing daytoday leadership, guidance, or oversight to study teams, vendors, or functional partners; people management responsibility may be direct or matrixed. * Strong working ...

Glaukos

Manager Study Start-up

San Clemente, CA · On-site

Prior experience providing day-to-day leadership, guidance, or oversight to study teams, vendors, or functional partners; people management responsibility may be direct or matrixed. * Strong working ...

Codera LLC

Senior Manager, Study Start Up

San Diego, CA · On-site

$130K - $160K/yr

The Senior Manager, Study Start Up & Records Management will interface with Site Directors and the study team to support operational aspects of study start-up and execution. Primary Responsibilities

Evommune, Inc.

Director, Toxicology

Palo Alto, CA · On-site

The Director will serve as the toxicology representative on cross-functional program teams and will ... Ensure studies are conducted in accordance with GLP requirements, applicable regulations, and ...

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Showing results 21-40

All JobsStudy JobsStudy Director JobsStudy Director Jobs in California

Study Director information

See California salary details

$44.4K

$126.7K

$229.5K

How much do study director jobs pay per year?

As of Aug 7, 2026, the average yearly pay for study director in California is $126,686.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,200.00 and $186,000.00 per year, depending on experience, location, and employer.

What is the difference between Study Director vs Laboratory Manager?

AspectStudy DirectorLaboratory Manager
CredentialsTypically requires advanced degrees (e.g., MS, PhD) and relevant certificationsRequires relevant degrees and management experience, but not necessarily advanced research credentials
Work EnvironmentLeads specific research or regulatory studies, often in contract labs or pharmaceutical companiesOversees daily lab operations, staff, and compliance across multiple projects
Industry UsageCommonly used in GLP, clinical, and research settingsUsed broadly in laboratory settings across industries

The Study Director focuses on designing, overseeing, and ensuring the integrity of specific studies, often requiring scientific expertise. The Laboratory Manager handles overall lab operations, staff management, and compliance. Both roles are essential but differ in scope and responsibilities.

What is a study director?

A Study Director is the individual responsible for the overall conduct of a scientific study, particularly in regulated environments such as pharmaceuticals, chemicals, or environmental research. They oversee the planning, execution, and reporting of studies to ensure they comply with regulatory standards, such as Good Laboratory Practice (GLP). The Study Director acts as the main point of control and communication, coordinating among team members and ensuring that the study meets its scientific and regulatory objectives. Their role is critical for the integrity and quality of the data generated.

How does a study director typically collaborate with cross-functional teams during a research project?

As a Study Director, you play a central role in coordinating research activities by regularly collaborating with scientists, technicians, quality assurance personnel, and regulatory teams. You are responsible for ensuring all team members are aligned on study objectives, timelines, and compliance requirements. Effective communication and leadership are essential, as you facilitate meetings, delegate tasks, and resolve issues that arise to keep the project on track. This collaborative environment not only fosters professional growth but also provides valuable exposure to various scientific and operational domains within the organization.

What does a study director do?

As a study director, your job is to manage studies, analyze results, and interpret reports so you can deliver a summary of the findings. This work has three categories. First, on the technical side, your job includes creating the plan for the study, coordinating with other scientists, and overseeing data collection. In the administrative role, you monitor junior employees and ensure each investigation finishes within budgetary constraints. In the compliance role, you ensure that each study happens under strict safety and ethics protocols. You may be asked to run multiple studies at the same time, adding to the complexity of this position.

What skills and qualifications does a successful study director have?

To thrive as a Study Director, you need a solid background in scientific research methods, regulatory compliance, and study protocol development, usually supported by an advanced degree in life sciences or a related field. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP) standards, and project management tools is highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for managing cross-functional teams and ensuring study integrity. These competencies are vital to ensure regulatory adherence, data accuracy, and successful project outcomes in research environments.
More about Study Director jobs
What are the most commonly searched types of Study jobs in California? The most popular types of Study jobs in California are:
What are popular job titles related to Study Director jobs in California? For Study Director jobs in California, the most frequently searched job titles are:
What job categories do people searching Study Director jobs in California look for? The top searched job categories for Study Director jobs in California are:
What cities in California are hiring for Study Director jobs? Cities in California with the most Study Director job openings:
Study Director jobs near you
Infographic showing various Study Director job openings in California as of July 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, 1% Temporary, and 3% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $126,686 per year, or $60.9 per hour.

Director, Clinical Study Management

Eikon Therapeutics

Millbrae, CA • On-site

$92K - $126K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 17 days ago

Job description

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon's discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.
Position
We are currently seeking an experienced leader for the clinical operations role of Director, Clinical Study Management within Clinical Study Management. The Director will manage all aspects of clinical operations study management for assigned Eikon clinical studies, and be responsible for exquisite inhouse execution of all such clinical trials and oversight of requisite clinical vendors. The role will also support the systematic pursuit of optimal performance, efficiency, and quality across the assigned clinical studies. Adherence to Good Clinical Practice (GCP), local and global policies and procedures to conduct high quality, inspection ready studies is essential. The Director is responsible for trial quality and audit responses and completion of CAPAs. The position has multiple stakeholder touch points within Clinical Research & Development (CR&D) staff and important interactions with, inter alia, Quality Assurance (QA), Finance, Regulatory, Clinical Supplies, Business Development and Legal in a matrix-based organization.
This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our Jersey City, New Jersey or Millbrae, California offices to ensure effective management and high-performance delivery of clinical studies.
About You
You are agile of mind, systematic, and a collaborative leader with global oncology clinical development experience and a passion for advancing patient care. You possess a deep understanding of clinical trial regulations, guidelines, and the principles of GCP, ensuring compliance throughout the clinical trial process.
What You'll Do
  • In collaboration with senior clinical operations management, build and lead inhouse clinical operations study management teams responsible for delivery of assigned clinical studies.
  • Manage clinical study management personnel across assigned clinical studies.
  • Ensure that compliance, quality and timeline objectives are met for all assigned studies.
  • Work collaboratively in a matrix organization with all internal stakeholders to deliver company clinical trial objectives on time, on budget, and with high quality.
  • Work with the CR&D Functional Area (FA) leads, as appropriate, to accelerate enrollment and drive high quality.
  • Take responsibility for any assigned clinical trial audits, working closely with the Clinical Quality Assurance group.
  • Represent Clinical Study Management in process workstreams and initiatives.
  • Effectively solve problems and use judgment relating to national and international regulations, guidelines, investigator interactions, and timelines.
  • Effectively manage resources to ensure appropriately skilled and high performing staff members are assigned to support the effective execution of the portfolio and achieve CR&D objectives.
  • Responsible for ensuring appropriate scientific and operational training for staff members.
  • Serve as a talent magnet and develop, coach, and retain top talent in the clinical program team.
  • Set clear performance standards and holds self and organization accountable for achieving results with flawless execution.
  • Embrace metrics and performance standards (KPIs) to drive continuous improvement in execution.

Qualifications
  • 12+ years of relevant experience with a Bachelor's degree or 10+ years of relevant experience with a Master's Degree with a demonstrated working experience in clinical study management within the biotechnology, pharmaceutical, or healthcare industry.
  • Relevant experience managing international clinical studies and programs in oncology.
  • Proven track record of contribution to and delivery of clinical trials that support global regulatory submissions, clean regulatory inspections and product approvals or marketing authorizations.
  • Relevant management experience in a clinical trial setting with the ability to service and collaborate with different CR&D stakeholders in a matrix organization.
  • Demonstrated situational leadership, independence, problem solving abilities, self-motivation, resourcefulness and ability to work in a fast-paced team environment.
  • Relevant management expertise should cover management of budget, resources, headcount, processes (and controls), productivity, quality and project delivery.
  • A complete understanding of ICH GCP and Global/Regional/Local regulatory requirements is required.
  • Strong communication skills requiring proficiency in written and spoken English.
  • Strategic thinking and high emotional intelligence.
  • Process improvement mindset and experience.
  • Strong leadership that will attract, motivate, inspire, develop and retain talented staff.
  • In addition, leadership skills that enable and drive alignment with the goals, purpose and mission of our company.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
  • 401k plan with company matching
  • Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
  • Mental health and wellness benefits
  • Weeklong summer and winter holiday shutdowns
  • Generous paid time off and holiday policies
  • Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
  • Enhanced parental leave benefit
  • Daily subsidized lunch program when on-site

The expected salary range for this role is $226,000 to $273,000 depending on skills, competency, and the market demand for your expertise.
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.
We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.

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