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Clinical Study Startup Jobs in California (NOW HIRING)

... Clinical Practice (GCPs), and applicable guidelines. * Support project teams with study startup and preparation activities, including protocol related reviews and laboratory readiness activities.

... Clinical Practice (GCPs), and applicable guidelines. * Support project teams with study startup and preparation activities, including protocol related reviews and laboratory readiness activities.

... startup environment. Key Responsibilities Leadership & Strategy * Develop and execute clinical ... study reports, and regulatory submissions, ensuring accuracy, timeliness, and compliance with ...

... startup company is a plus * Exceptional clinical trial management skills with a focus on strategic oversight of trial execution on time and on budget, study coordinator and/or site monitoring ...

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Clinical Study Startup information

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How much do clinical study startup jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for clinical study startup in California is $61.70, according to ZipRecruiter salary data. Most workers in this role earn between $50.05 and $69.52 per hour, depending on experience, location, and employer.

What is a clinical study startup?

A Clinical Study Startup job involves managing the initial phases of a clinical trial, ensuring all regulatory, ethical, and logistical requirements are met before patient enrollment begins. Responsibilities typically include submitting regulatory documents, coordinating with ethics committees, negotiating contracts, and ensuring trial sites are fully prepared. This role requires strong knowledge of clinical research regulations, timelines, and collaboration with internal and external stakeholders. Effective study startup is crucial for minimizing delays and ensuring compliance with industry standards.

What are the key skills and qualifications needed to thrive in clinical study startup, and why are they important?

Success in a Clinical Study Startup role requires a strong understanding of clinical research processes, regulatory requirements, project management, and often a life sciences degree or related field. Familiarity with clinical trial management systems (CTMS), electronic trial master files (eTMF), and regulatory submission platforms is essential, along with certifications like GCP (Good Clinical Practice) being advantageous. Attention to detail, proactive problem-solving, and excellent organizational and communication skills help candidates excel. These qualifications ensure smooth study initiation, regulatory compliance, and effective cross-functional collaboration within demanding timelines.

What are the typical responsibilities of someone working in clinical study startup?

Professionals in Clinical Study Startup are primarily responsible for coordinating and executing study initiation activities, including regulatory document collection, ethics submissions, site contracting, and start-up logistics. They work closely with investigators, sponsors, and cross-functional teams to ensure all regulatory and site requirements are met before the clinical trial begins. This role often involves tight deadlines and frequent communication with stakeholders both internally and externally. It's a fast-paced position that is ideal for individuals who enjoy detail-oriented work and project coordination in a collaborative environment.

What are the most commonly searched types of Clinical Study Startup jobs in California?

The most popular types of Clinical Study Startup jobs in California are:

What cities in California are hiring for Clinical Study Startup jobs?

Cities in California with the most Clinical Study Startup job openings:

Infographic showing various Clinical Study Startup job openings in California as of August 2026, with employment types broken down into 89% Full Time, 3% Part Time, 3% Temporary, and 5% Contract. Highlights an 94% In-person, 3% Hybrid, and 3% Remote job distribution, with an average salary of $128,331 per year, or $61.7 per hour.

Executive Director & Head Clinical Data Management

Annexon Biosciences

San Francisco, CA โ€ข On-site

$94K - $128K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 3 days ago

New


Job description

Company:ย 

At Annexon Biosciences we are a biopharmaceutical company advancing a late-stage clinical platform of novel therapies for people living with devastating classical complement-mediated neuroinflammatory diseases of the body, brain, and eye. Our novel scientific approach targets upstream C1q to block the classical complement inflammatory cascade before it starts, and its therapeutic candidates are designed to provide meaningful benefits across multiple autoimmune, neurodegenerative and ophthalmic diseases. With proof-of concept data in Guillain-Barre syndrome, Huntington's disease and geographic atrophy, we are rigorously advancing our mid-to late-stage clinical trials to bring new potential treatments to patients as quickly as possible. At Annexon, you'll be part of a team committed to making an impact together.ย ย ย 

For more information on Annexon and our pipeline, check out our site Annexon Biosciences & Annexon Pipeline. We trade on Nasdaq under the ticker symbol ANNX and are headquartered in Brisbane, CA.ย 

We're seekingย exceptional talent from all backgrounds to fuel our growth. At Annexon, we're building a diverse, equitable, and inclusive workplace. We value unique perspectives and unconventional paths. If you're the best candidate for the job, even if you don't perfectly fit the traditional mold, we encourage you to apply.ย Learn more about our commitment to diversity, equity, inclusion, and our companyย culture!ย 

Position:ย 

Reporting to the SVP, Biometrics, this leader independently oversees a team of data managers and technology experts responsible for acquisition and quality of all Annexon clinical trial data. A highly empowered, visible and collaborative role, the Executive Director & Head Clinical Data Management partners cross-functionally to advance medicines to our patients.

Responsibilities include:ย 

  • Set the vision for Clinical Data Management through building and maintaining a best-in-class organization that functions as a key strategic partner within Annexon
  • Provide operational, strategic, and technical direction to data managers and technology SMEs while maintaining ultimate responsibility for all clinical data within Annexon
  • Accountable for all Clinical Data Management activities from study startup through study conduct and closeout delivering quality data snapshots, interim database locks and final database locks
  • Design and deploy appropriate clinical data management operating models including full outsourcing, hybrid delivery and fully in-house
  • Ensure clinical data management strategies that incorporate both current best practices and innovative approaches consistent with GCP and GCDMP
  • Design and deploy sponsor oversight for outsourced studies including operating model, oversight planning and execution, vendor governance and interactions, risk management and documentation
  • Define, advance and codify procedural framework (operating model, process definitions and associated SOPs/WIs, Clinical Data Management best/expected practices) for the department
  • Serve on the Biometrics leadership team to provide guidance on direction and operations of the department
  • Provide expert guidance to project teams and executive leadership
  • Participate cross-functionally with key partners to advance Annexon products
  • Contribute to and participate in the development and maintenance of a positive team-focused company culture

Education, Experience, and Skills:ย 

Required:ย 

  • Bachelor's degree with 12+ years of experience in the pharmaceutical or biotechnology industry in a Clinical Data Management leadership capacity
  • Extensive experience with industry clinical data management delivery models and associated sponsor oversight (full outsourcing etc.)
  • Experience building and leading high performing teams; and identifying, attracting, developing, and retaining top talent
  • Proficiency in Clinical Data Management related technology like EDC, eSource, eCOA, IRT etc.
  • Experience leading programs through submission and approval
  • Deep understanding of GCP and GCDMP
  • Solid understanding of eCRF data acquisition best practices

Preferred:ย ย 

  • Ability to communicate with clarity and influence including explaining complex quantitative issues in simple terms
  • Solid understanding of Regulatory (FDA/EMA/ICH) guidance with the ability to interpret and apply in real-time drug development setting
  • Solid understanding of regulatory submission and approval process
  • Collaborative negotiator with excellent judgment around compromising, standing firm, or finding a new way forward.
  • Leadership acumen including emotional intelligence and business awareness. Ability to effectively collaborate and influence throughout multiple levels of the organization.
  • Strategic and creative drug-development mindset/approach. Willingness to deviate from the status quo
  • Ability to balance appropriate levels of structure/process with efficiency and simplicity
  • Awareness of external industry landscape with respect to best practices and emerging topics

Salary Range: $301,500 - $330,000

Location:ย Annexon Biosciences is located in Brisbane, California. This role operates under a hybrid work arrangement and requires regular onsite collaboration at our office. Candidates should be located within commuting distance and able to work in the office multiple days each week.

Benefits:ย 

  • A stimulating and rewarding workplace includes flexible work schedules, remote opportunities and the ability to achieve a work-life balance.
  • Shuttle service from BART, CalTrain and the Ferry.
  • Annexon offers a competitive base salary and equity participation, employee stock purchase plan, as well as a comprehensive health benefit package that includes medical, dental, vision, 401(k), flexible spending plans, and other benefits.ย 

Annexon Biosciences is an Equal Opportunity Employer, and we prohibit discrimination or harassment of any kind.ย  We are committed to fostering an environment where ALL people are welcome and supported. We cultivate a culture of inclusion for all employees that respects their individual strengths, views, and experiences. We believe that our differences enable us to be a better team - one that makes better decisions, drives innovation, and delivers better business results. Creativity and innovation flourish in an environment of openness, inclusion, and mutual respect.ย