×
Register Here to Apply for Jobs or Post Jobs. X

Clinical Research Specialist; CRS

Job in Irvine, Orange County, California, 92713, USA
Listing for: Masimo
Full Time position
Listed on 2026-02-01
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 68000 - 85000 USD Yearly USD 68000.00 85000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Research Specialist (CRS)

Job Summary

The Clinical Research Specialist (CRS) is responsible for supporting and/or conducting clinical study activities and basic data collection at clinical sites, as well as managing assigned clinical projects & operations, including pre-monitoring activities, data entry, inventory management, device procurement, shipping, and financial management. Supports CRAs with IRB submissions, site training, tracking study progress and performance, and generating reports which includes interacting and communicating with site staff and key study personnel.

Ensures all activities are conducted in accordance with regulations (FDA, EU MDR, and other international regulations), Good Clinical Practices (GCP), department standard operating procedures, and Masimo’s guiding principles including Masimo’s code of conduct and highest ethics.

Duties & Responsibilities
  • Plan, implement and conclude clinical studies in support of project timelines/market release goals.
  • Prepare and document study plans, contracts, budgets, informed consents, support IRB submissions, case report forms (CRFs), and other study related materials to assure quality, consistency, compliance, organization, storage, and accuracy across all assigned projects.
  • Contribute to clinical study design, proposals, protocols, etc., understanding basic scientific content, experimental design, and analytical approaches used.
  • Effectively work and communicate with investigator, staff, and patients in professional, sensitive, and mature manner.
  • Conduct or assist with site monitoring under direct supervision of Manager or Senior CRAs (qualification, initiation, monitoring and close out visits) to ensure and document site is trained to follow study procedures per protocol.
  • Attend meetings and recap discussions for internal and external distributions.
  • Support TMF maintenance including Site and Sponsor communications along with all study related documentation.
  • Order equipment for Masimo studies, managing inventory and shipments to study sites; follow SOP to ensure device accountability and proper labeling.
  • Track spending for reporting and accruals.
  • Perform data entry, verification, and organization of data files.
  • Support the department with conduct of Sponsored and Investigator Initiated Studies; work with Clinical Research Associates and Managers to support them on projects and tasks.
  • Support data collection duties, including equipment setup and operations, execution of study per procedures and data collection.
  • Support/conduct moderate data analysis using spreadsheet and statistical programs, and organize reports of data in simple clear fashion with appropriate tables, charts, and graphs.
  • Pack, ship, move, unpack, set up and executive equipment for study at clinical site, repacking, and shipping back to Masimo.
  • Perform other duties and projects as assigned.
Minimum Qualifications
  • Familiarity with medical, pharmaceutical or medical device research.
  • Basic understanding of Good Clinical Practice (GCP) guidelines, medical device regulations.
  • Good verbal skills with the ability to articulate work product with team, supervisor, management, and other departments or to investigator.
  • Must be proficient with Microsoft Office Suite.
  • Demonstrates basic judgment and decision-making ability in the execution of job responsibilities.
  • Ability to write clearly and succinctly.
  • Ability to travel to data collection sites, local and domestic, may require up to 25-50% of time.
  • Must be able to lift and carry up to 20 pounds.
Preferred Qualifications
  • Clinical or scientific background (e.g., respiratory therapy, nursing, pharmacology, physiology).
  • Basic knowledge of ISO, EU MDR, Canadian Medical Device Regulation, and other international requirements.
Education

Bachelor’s degree preferred.

Compensation

The anticipated salary range for this position is $68,000 - $85,000 plus benefits. Actual placement within the range is dependent on multiple factors, including but not limited to skills, education, and experience. This position also qualifies for up to 10% annual bonus based on Company, department, and individual performance.

Masimo offers benefits such as Medical, Dental, Vision, Life/AD&D, Disability…

To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary