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

Alumis

Vice President, Medical Affairs

Bodega Bay, CA

$315K - $370K/yr

... 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

The Steely Group

Sr. Research Associate

Novato, CA · On-site

$45 - $51/hr

Design and execute ligand-binding assays, hybrid assays, and cell-based assays for non-clinical ... study reports. * Effectively prioritize and manage workload across diverse assay types and ...

VCA Animal Hospitals

Associate Veterinarian

Santa Rosa, CA · On-site

$66K - $180K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Opportunities to participate in a robust Clinical Studies program Discover Additional Benefits ... Management reserves the right to revise the or require that other tasks be performed when the ...

Sonoma Valley Hospital

Echocardiograph Technician

Sonoma, CA · On-site

$46.97 - $64.58/hr

Experience : 1-2 years experience in a similar clinical setting. Licenses & Certifications : Valid ... Ability to manage priorities and workflow. Ability to understand and adhere to established policies ...

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Clinical Study Manager information

See Santa Rosa, CA salary details

$31

$68

$105

How much do clinical study manager jobs pay per hour?

As of Aug 16, 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.

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:

Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Santa Rosa, CA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 18% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $142,171 per year, or $68.4 per hour.

Clinical Research Specialist

Integrated Resources INC

Santa Rosa, CA • On-site

Contractor

Re-posted 4 days ago

Job description

Company Description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Duration: 12 Months+ Contract ( possibility of extension)

JOB DESCRIPTION:
Top 3 qualifications:
Previous clinical research experience
Ability to prioritize and strong critical thinking skills
Attention to detail and strong communication skills

Responsibilities:
Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines, and policies.

  • Assist in preparation of study materials and/or training. Interface with, and assure training of investigators, site staff, and client clinical staff.
  • Assist in site initiation (e.g. start-up document preparation, distribution, receipt, and review).
  • May arrange conference calls, staff meetings and training events.
  • Assist data management group with review of clinical data/information and oversight of data correction.
  • May assist with oversight of activities performed by Contract Research Organizations (e.g. CROs, core labs).
  • Able to refer to Standard Operating Procedures (SOPs) and Department Operating Procedures (DOPs) for guidance on everyday study tasks.
  • Contribute to ongoing SOP development and review. Participate in training to enhance knowledge base.
  • Must be willing to assist with other duties as needed such as filing and document tracking.

Qualifications:
Must have ability to prioritize and critical thinking skills and previous clinical research experience. Must have strong written, oral, and interpersonal communication skills and high attention to detail and accuracy.
3-5 years of experience

Education required: 4 year degree

Qualifications

Must have ability to prioritize and critical thinking skills and previous clinical research experience. Must have strong written, oral, and interpersonal communication skills and high attention to detail and accuracy. 
3-5 years of experience 

Additional Information

Additional Information

Feel free to forward my email to your friends/colleagues who might be available. We do have referral bonus, if you refer any of your friends or colleague who are looking out for the same job.

Thanks,

Warm Regards,

Nisha

Integrated Resources, Inc.

IT REHAB CLINICAL NURSING

Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012 ,2013 and 2014 (8th Year)

Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70

Direct: (732)-429-1649

Tel: (732) 549 2030 x 230

Fax: (732) 549 5549


Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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