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Study Monitor Jobs in California (NOW HIRING)

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Conduct clinical study monitoring to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete source data ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Conduct clinical study monitoring to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete source data ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Conduct clinical study monitoring and/or oversee CRAs to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site

Conduct clinical study monitoring and/or oversee CRAs to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete ...

Intuitive

Sr. Clinical Study Manager

Sunnyvale, CA · On-site +1

Conduct clinical study monitoring to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete source data ...

Intuitive

Conduct clinical study monitoring to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete source data ...

Intuitive Surgical

Conduct clinical study monitoring to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete source data ...

RPM ReSearch

Study Director

West Sacramento, CA · On-site

$74K - $110K/yr

Monitor study milestones and ensure accurate recording and verification of all experimental data. * Communicate ongoing study activities and results to sponsors. * Analyze and interpret study data ...

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Study Monitor information

What is a study monitor?

A Study Monitor, also known as a Clinical Research Associate (CRA), is responsible for overseeing clinical trials to ensure they comply with regulatory guidelines, study protocols, and ethical standards. They monitor site activities, review data accuracy, and ensure participant safety. Study Monitors work closely with investigators, site staff, and sponsors to ensure the integrity of trial results and adherence to Good Clinical Practice (GCP) guidelines.

What are the key skills and qualifications needed to thrive as a study monitor?

To thrive as a Study Monitor, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as GCP), and data integrity principles, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are commonly expected. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills. These competencies ensure high-quality study oversight, compliance with regulations, and smooth collaboration among clinical research teams.

What are some common challenges study monitors face during clinical trials?

Study Monitors often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing discrepancies in data, and navigating tight timelines for site visits and reporting. They must adapt quickly to evolving regulatory requirements and effectively communicate any issues or deviations to investigators and sponsors. Being proactive in identifying potential risks and fostering strong relationships with site staff can help minimize these challenges. As a result, successful Study Monitors need to be resourceful, detail-oriented, and skilled at balancing regulatory compliance with practical problem-solving in dynamic trial environments.

How do you become a study monitor?

To become a study monitor, candidates typically need to be students with good academic standing and demonstrate responsibility. The process often involves applying through the school or organization, sometimes including an interview or recommendation, and may require training on supervision and safety protocols.

What are popular job titles related to Study Monitor jobs in California?

For Study Monitor jobs in California, the most frequently searched job titles are:

What job categories do people searching Study Monitor jobs in California look for?

The top searched job categories for Study Monitor jobs in California are:

What cities in California are hiring for Study Monitor jobs?

Cities in California with the most Study Monitor job openings:

Study Monitor jobs near you
Infographic showing various Study Monitor job openings in California as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 10% Part Time, 3% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Associate Director, Preclinical Study Monitor and Operations

Attovia Therapeutics

San Carlos, CA

Full-time

Posted 8 days ago

Job description

Attovia Therapeutics, Inc., is seeking a highly organized and detail-oriented Associate Director of Preclinical Study Monitor and Operations to join our Preclinical Development team. In this role, you will be responsible for overseeing outsourced preclinical studies to ensure they are conducted efficiently, ethically, and to the highest quality standards, including Good Laboratory Practice (GLP) standards. You will collaborate closely with Study Directors, internal scientists, and external vendors to drive study execution and safeguard data integrity.

In addition, this individual will manage the operational lifecycle of our non-clinical pipeline. In this role, you will lead the logistical coordination of both internal and external research projects. You will be responsible for vendor selection, contract execution, budget tracking, and material logistics. Your work will directly ensure that our preclinical programs move smoothly from concept to execution without operational delays.

Key Responsibilities
  • Vendor Oversight: Act as the primary scientific and operational contact for CRO partners, ensuring timelines, budgets, and deliverables are consistently met.
  • Protocol & Report Review: Review draft protocols and study reports for completeness, accuracy, and alignment with internal research strategies before finalization.
  • Compliance & Monitoring: Conduct routine study visits/inspections (both in-person and remotely) to verify that laboratory procedures adhere to protocol specifications, SOPs, and Good Laboratory Practice (GLP) standards.
  • Data Management: Track deliverables for samples, bioanalysis, and data collection. Identify potential discrepancies protocol deviations and work with stakeholders to resolve them promptly.
  • Cross-Functional Collaboration: Communicate study updates regularly with internal stakeholders, toxicologists, discovery scientists, and project teams.
  • Logistics & Material Management: Coordinate the global shipment of test articles, biological samples, and critical reagents between internal sites and contract research organizations (CROs).
  • Vendor & Contract Management: Lead the sourcing and onboarding of external vendors. Manage the execution of Master Service Agreements (MSAs), Statements of Work (SOWs), and purchase orders.
  • Budget & Timeline Tracking: Maintain integrated project timelines and track program budgets. Monitor operational expenditures and forecast upcoming resource needs.
  • Operational Troubleshooting: Serve as the central point of contact for operational bottlenecks, resolving custom clearance issues, shipping delays, or invoice discrepancies.
Qualifications
  • Bachelor's degree in Life Sciences, Toxicology, Pharmacology, or a related field
  • 10+ years of related work experience in drug discovery/development.
  • Solid understanding of global regulatory guidelines (e.g., FDA, OECD, GLP regulations) governing nonclinical safety and toxicology studies.
  • Excellent project management, critical thinking, and communication skills to effectively negotiate timelines and troubleshoot challenges.
  • Exceptional organizational skills, strong negotiation capabilities, and the ability to manage multiple fluid projects simultaneously.
About Attovia

Attovia is a clinical-stage biopharmaceutical company developing next-generation biotherapeutics for immune-mediated diseases with high unmet need.  Our product candidates are internally discovered using our proprietary ATTOBODY platform, an evolution-driven, high-throughput biologics platform that enables the rapid discovery and creation of diverse biparatopic complex biologics.  Our pipeline spans chronic pruritic diseases, inflammatory skin diseases, inflammatory bowel disease, and other immune-mediated conditions.

Our company values define how we make decisions, work with one another, and pursue our mission:
  • Integrity: We put patients first, uphold the highest ethical standards, and communicate with honesty and transparency
  • Learning & Growth: We ask questions, challenge the status quo, seek and provide constructive feedback, and invest in the development of ourselves and others
  • Drive for Excellence: We set ambitious goals, take ownership, honor our commitments, move with urgency, and deliver rigorous, high-quality, and data-driven work
  • Innovation: We pursue transformative science, think creatively, and do more with less through resourcefulness and continuous improvement
  • Teamwork & Collaboration: We communicate openly, debate constructively, mentor and learn from one another, and recognize that our strongest results come from working together  

We take pride in fostering a strong team and dynamic work environment, and we are seeking individuals who align with our values and contribute to a positive and impactful workplace.  
Attovia is located in San Carlos, CA.
Attovia is an equal opportunity employer. We consider all qualified applicants for employment without regard to race, color, ancestry, national origin, religion or creed, age, sex, pregnancy, childbirth, breastfeeding or related medical conditions, sexual orientation, gender, gender identity or gender expression, marital status, medical condition, genetic information, physical or mental disability, military or veteran status, reproductive health decision-making, or any other characteristic protected by applicable federal, state, or local law. 
Learn more about Attovia: www.attovia.com

$180,000 - $225,000 a year
Leveling and salary is commensurate with experience.

Notice to Employment Agencies

The Attovia talent acquisition program is managed through internal resources, and unsolicited referrals and resumes are not accepted from employment agencies, unless advance written authorization is granted from the Human Resources department. Attovia shall not be liable for any fees arising from any unsolicited or unauthorized candidate information received relative to position vacancies.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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