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Clinical Study Manager Jobs in Santa Rosa, CA (NOW HIRING)

... Alumis' clinical studies as well as our commercial group. Applicants should be a "leader/doer ... Develop and present Medical Affairs operational plans to Development and Executive management

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Clinical Study Manager information

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How much do clinical study manager jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical study manager in Santa Rosa, CA is $68.35, according to ZipRecruiter salary data. Most workers in this role earn between $55.43 and $77.02 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

What are popular job titles related to Clinical Study Manager jobs in Santa Rosa, CA?

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What job categories do people searching Clinical Study Manager jobs in Santa Rosa, CA look for?

The top searched job categories for Clinical Study Manager jobs in Santa Rosa, CA are:

What cities near Santa Rosa, CA are hiring for Clinical Study Manager jobs?

Cities near Santa Rosa, CA with the most Clinical Study Manager job openings:

Infographic showing various Clinical Study Manager job openings in Santa Rosa, CA as of August 2026, with employment types broken down into 82% Full Time, 17% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $142,171 per year, or $68.4 per hour.

Clinician-Research Associate TrueNorth Health Foundation

Healthpromoting

Santa Rosa, CA • On-site

$60 - $80/hr

Other

Posted 5 days ago


Job description

Clinician–Research Associate TrueNorth Health Foundation

The TrueNorth Health Foundation is looking for a Clinician–Research Associate to join our residential clinical program in medically supervised prolonged water-only fasting and whole-plant-food, SOS‑free refeeding.

This role is designed for a clinician — or clinician‑in‑training — with at least a year of research experience who wants genuine mentorship in fasting and refeeding medicine alongside the opportunity to contribute meaningfully to projects that document, curate, and advance the clinical science of fasting.

Key Responsibilities Clinical training
  • Participate in daily patient monitoring and documentation workflows under senior clinician supervision
Case reports
  • Identify novel cases with attending clinicians
  • Coordinate with patients and clinicians to confirm timelines, fill gaps, and support follow‑up
  • Extract and organize case data — history, clinical course, vitals, labs, medications, adverse events, outcomes — into a structured case file
  • Research the relevant condition and fasting/refeeding literature to contextualize each case
  • Draft first versions of case reports for internal review and peer‑reviewed submission, CARE‑guidelines aligned
  • Help maintain the Foundation's fasting literature database,
  • Review and improve existing records: fix metadata, attach PDFs, standardize tagging by condition, protocol, duration, outcomes, and adverse events
  • Add new publications with brief structured annotations covering study design, population, protocol, key findings, and limitations
Systems and workflow
  • Collaborate with the research team to define and apply consistent database standards: required fields, controlled vocabulary, PDF naming and storage
  • Build and maintain a case report pipeline: nomination criteria, tracking system, data‑extraction template, follow‑up checklist, and internal review steps
Qualifications Required
  • Clinician (MD/DO/ND/PA/NP/RN/DC) or enrolled in a clinical degree program
  • 1–2 years of research experience — clinical, thesis, academic lab, or equivalent
  • Strong writing skills and a careful, methodical approach to clinical records and data abstraction
  • Able to work on‑site in a residential clinical environment
Preferred
  • Experience with case reports, chart reviews, or manuscript drafting
  • Literature searching, evidence synthesis, or reference management (Zotero, EndNote)
  • A demonstrated interest in nutritional medicine

Location: TrueNorth Health Center, Santa Rosa, CA. On‑site, residential setting. Full‑time. Competitive salary + housing and whole‑plant‑food, SOS‑free meals provided.

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