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Study Manager Jobs in California (NOW HIRING)

Veranex

Senior Clinical Study Manager

Raleigh, NC · On-site

$125K - $179K/yr

The Senior Clinical Study Manager is responsible for planning, executing, and overseeing clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

This Lead Clinical Study Manager-4 (CSM IV) / Senior Clinical Study Manager role will develop and execute strategies for US and global first-human-use and pivotal pre-market clinical trials to help ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site

This Lead Clinical Study Manager-4 (CSM IV) / Senior Clinical Study Manager role will develop and execute strategies for US and global first-human-use and pivotal pre-market clinical trials to help ...

Glaukos

Manager Study Start-up

San Clemente, CA

Clinical Study Manager The Clinical Study Manager is responsible for the end-to-end management and execution of clinical studies supporting medical device development. This role leads cross ...

Glaukos

Manager Study Start-up

San Clemente, CA

Clinical Study Manager The Clinical Study Manager is responsible for the end-to-end management and execution of clinical studies supporting medical device development. This role leads cross ...

Intuitive

Sr. Clinical Study Manager

Sunnyvale, CA · On-site +1

The Clinical Study Manager-4 (CSM IV) role will develop and execute strategies for clinical and outcomes research studies to help regulatory approvals and key strategic evidence initiatives. As a ...

Spyglass Pharma

Clinical Study Manager

Aliso Viejo, CA · On-site

$140K - $160K/yr

Summary: The Clinical Study Manager (CSM) plays a key role in the planning and execution of SpyGlass Pharma's clinical trials. Working closely with the Director of Clinical Research and cross ...

Intuitive Surgical

The Clinical Study Manager-4 (CSM IV) role will develop and execute strategies for clinical and outcomes research studies to help regulatory approvals and key strategic evidence initiatives. As a ...

Intuitive

The Clinical Study Manager-4 (CSM IV) role will develop and execute strategies for clinical and outcomes research studies to help regulatory approvals and key strategic evidence initiatives. As a ...

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Study Manager information

See California salary details

$24.2K

$58.7K

$114.5K

How much do study manager jobs pay per year?

As of Jul 16, 2026, the average yearly pay for study manager in California is $58,746.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,400.00 and $67,600.00 per year, depending on experience, location, and employer.

How does a Study Manager typically collaborate with cross-functional teams during the course of a clinical trial?

As a Study Manager, you'll work closely with cross-functional teams including clinical research associates, data managers, regulatory affairs, and biostatisticians to ensure the trial progresses smoothly and meets regulatory requirements. Regular meetings, status updates, and shared project management tools facilitate clear communication and timely issue resolution. You will often serve as the central point of contact, coordinating tasks and resolving conflicts between departments to keep the study on track. Collaboration skills are essential, as you’ll need to balance input from multiple stakeholders while maintaining study timelines and quality standards.

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

To thrive as a Study Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These qualifications ensure the successful planning, execution, and oversight of clinical studies within regulatory and timeline requirements.

What does a Study Manager do?

A Study Manager is responsible for overseeing the planning, execution, and completion of research studies, often in clinical or academic settings. They coordinate between various stakeholders, including research teams, sponsors, and regulatory authorities, to ensure studies are conducted efficiently and in compliance with relevant guidelines. Study Managers manage timelines, budgets, and resources, while also handling documentation and reporting requirements. Their role is critical to ensuring that studies meet their scientific objectives and adhere to ethical standards.
What are the most commonly searched types of Study jobs in California? The most popular types of Study jobs in California are:
What cities in California are hiring for Study Manager jobs? Cities in California with the most Study Manager job openings:
Study Manager jobs near you
Senior Clinical Study Manager

Senior Clinical Study Manager

Veranex

Raleigh, NC • On-site

$125K - $179K/yr

Full-time

Re-posted 22 days ago

Job description

Veranex's mission as an Innovation CRO is to improve patient outcomes by accelerating our clients' innovations to market. As the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
About This Role:
The Senior Clinical Study Manager is responsible for planning, executing, and overseeing clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. This role involves collaborating with various stakeholders, including sponsors and regulatory authorities, to drive the successful completion of clinical studies. By managing the operational aspects of the trial, a Clinical Study Manager ensures that high-quality data is generated, contributing to the advancement of medical science and the development of new therapies.
Location: Remote, US
What You Will Do:
Study Management
  • Lead day-to-day management of study activities and deliverables.
  • Serve as a liaison with stakeholders across all functional areas of the study.
  • Manage study budget and timelines.
  • Manage vendors, including the implementation and coordination of vendor scope of work (SOW).
  • Serve as a point of contact for issue escalation.
  • Interact directly with institutions and investigators, execute clinical research initiatives, and ensure alignment with strategic goals.

Study Start-Up, Site Management & Execution
  • Coordinate and support execution of study projects, including:
    • Site identification and initiation
    • Ethics and regulatory approvals
    • Contracting
    • Site budgeting and invoicing
    • Site staff training
    • Site initiations, routine monitoring, and close-out activities
  • Identify and establish the suitability of study investigators and sites and liaise with them to ensure compliance with all study requirements, approvals, and agreements.
  • Lead the development and implementation of key study documents, including study-specific plans, monitoring plans, study reference manuals, and source document templates.
  • Lead the execution of clinical studies, evaluation and analysis of clinical data, and preparation/review of clinical study reports.

Quality, Compliance & Oversight
  • Oversee maintenance of clinical and regulatory files, ensuring accurate and timely tracking and documentation.
  • Oversee the development of clinical reports supporting regulatory submissions.
  • Oversee monitoring of study conduct and progress, including proactive identification and resolution of issues impacting quality, timelines, budget, or compliance.
  • Identify and mitigate quality risks and/or issues associated with assigned studies and activities.
  • Ensure study conduct complies with ethical and regulatory standards, SOPs, GCP, and local regulations.

Performance Tracking & Reporting
  • Lead the collection, tracking, and reporting of key performance indicators (KPIs), including:
    • query resolution
    • safety data collection/issues
    • product/device reconciliation and shipment
    • site and patient enrollment
    • protocol deviations

Strategic & Business Support
  • Contribute to business development activities as a subject matter expert (SME).
  • Generate strategy and proposal documentation as directed.

Qualifications
Required:
  • Bachelor's degree in health sciences or related discipline
  • Minimum of 5 years of relevant experience in medical device clinical study planning, preferably within a MedTech-oriented CRO
  • Experience maintaining documentation in compliance with FDA and ISO standards
  • Ability to independently manage multiple priorities in a fast-paced environment
  • Strong organizational, analytical, and problem-solving skills
  • Excellent written and verbal communication skill

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.

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