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Clinical Research Manager Jobs in Santa Rosa, CA

NorthBay Health

Physician, Endocrinology - Napa

Napa, CA · On-site

$534K/yr

Provide guidance on managing long-term conditions like diabetes and thyroid diseases to improve quality of life. * Research & Innovation: Participate in clinical research studies and trials related ...

NorthBay Health

Physician, Endocrinology - Napa

Napa, CA · On-site

$534K/yr

Provide guidance on managing long-term conditions like diabetes and thyroid diseases to improve quality of life. * Research & Innovation: Participate in clinical research studies and trials related ...

Endologix

Sr. R&D Engineer

Santa Rosa, CA · On-site

$114K - $156K/yr

We are committed to delivering excellent clinical outcomes through precision in product design ... In this role, you'll provide advanced technical leadership to support the lifecycle management ...

Endologix

Sr. R&D Engineer

Santa Rosa, CA · On-site

$114K - $156K/yr

We are committed to delivering excellent clinical outcomes through precision in product design ... In this role, you'll provide advanced technical leadership to support the lifecycle management ...

Endologix

Sr. R&D Engineer

Santa Rosa, CA · On-site

$114K - $156K/yr

We are committed to delivering excellent clinical outcomes through precision in product design ... In this role, you'll provide advanced technical leadership to support the lifecycle management ...

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All JobsClinical Research JobsClinical Research Manager JobsClinical Research Manager Jobs in Santa Rosa, CA

Clinical Research Manager information

See Santa Rosa, CA salary details

$53.6K

$117.4K

$206.6K

How much do clinical research manager jobs pay per year?

As of Aug 25, 2026, the average yearly pay for clinical research manager in Santa Rosa, CA is $117,354.00, according to ZipRecruiter salary data. Most workers in this role earn between $88,600.00 and $133,900.00 per year, depending on experience, location, and employer.

What does a clinical research manager do?

A clinical research manager oversees clinical trials, which involve testing new medications or medical devices. Their responsibilities include ensuring all ethical practices and legal protocols are followed and that all paperwork is filled out completely and accurately. They also maintain standards for the data collection and procedures during the clinical trial and make sure all team members, including the doctors and nurses on the trial, are kept informed.

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

To thrive as a Clinical Research Manager, you need a solid understanding of clinical trial protocols, regulatory requirements (such as GCP), and a background in life sciences or healthcare, often supported by a relevant degree. Familiarity with clinical trial management systems (CTMS), EDC software, and certifications like ACRP or SOCRA are typically expected. Strong leadership, excellent organizational skills, and effective communication abilities set outstanding managers apart. These competencies are critical for ensuring compliance, data integrity, and the successful coordination of multidisciplinary research teams.

What are some common challenges clinical research managers face when overseeing multiple clinical trials simultaneously?

Clinical Research Managers often encounter challenges such as balancing competing timelines, ensuring regulatory compliance across different studies, and effectively allocating resources among projects. Managing communication between diverse teams—such as investigators, sponsors, and regulatory bodies—can also be demanding, especially when trials are at different stages. Developing strong organizational skills and leveraging project management tools are key to successfully navigating these complexities and maintaining high standards for data quality and participant safety.

What is the difference between Clinical Research Manager vs Clinical Research Coordinator?

AspectClinical Research ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with experience in project managementBachelor's in health sciences or related field, often with certification like CCRP
Work EnvironmentOversees multiple studies, manages teams, and ensures compliance at a higher levelAssists with daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites

The Clinical Research Manager focuses on overseeing entire studies and managing teams, while the Clinical Research Coordinator handles daily study tasks and participant interactions. Both roles require relevant certifications and are essential in clinical research settings, but they differ in scope and responsibilities.

More about Clinical Research Manager jobs

What are the most commonly searched types of Clinical Research jobs in Santa Rosa, CA?

The most popular types of Clinical Research jobs in Santa Rosa, CA are:

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

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

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

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

Clinical Research Manager jobs near you
Infographic showing various Clinical Research 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 $117,354 per year, or $56.4 per hour.

Clinical Research Specialist

Integrated Resources INC

Santa Rosa, CA • On-site

Contractor

Re-posted 12 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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