Masimo · 2 days ago
Clinical Research Specialist (CRS)
Irvine, CA
Full-time
Onsite
New Grad, Entry Level
$68K/yr - $85K/yrMasimo is a company dedicated to improving patient outcomes through noninvasive monitoring solutions. They are seeking a Clinical Research Specialist (CRS) who will support and conduct clinical study activities, manage clinical projects, and ensure compliance with regulations and Good Clinical Practices.
BiotechnologyHealth CareManufacturingMedical Device
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
Qualification
Required
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
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
Benefits
Medical
Dental
Vision
Life/AD&D
Disability Insurance
401(k)
Vacation
Sick
Holiday
Paid Maternity Leave
Flexible Spending Accounts
Voluntary Accident
Critical Illness
Hospital
Long-Term Care
Employee Assistance Program
Pet Insurance
On-site Wellness Clinic
Fitness Center
Cafe
Company
Masimo
Masimo Corporation, a medical technology company, develops, manufactures, and markets noninvasive patient monitoring products.
Founded in 1989
1001-5000 employees
H1B Sponsorship
Masimo has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (35)
2024 (22)
2023 (27)
2022 (25)
2021 (24)
2020 (15)
Funding
Current Stage
Public CompanyTotal Funding
$754.95MKey Investors
Politan Capital ManagementRobecoBill & Melinda Gates Foundation
2022-08-15Post Ipo Equity· $750M
2017-08-26Post Ipo Equity
2016-11-11Grant· $4.95M
Leadership Team
Michelle Brennan
Board Chair
Recent News
2026-01-13
2026-01-13
Company data provided by crunchbase