Thermo Fisher Scientific·San Diego, California
The CRA II is responsible for monitoring investigator sites to ensure protocol compliance, data reliability, and subject safety. This includes conducting on-site and remote visits, managing essential documentation, and maintaining relationships with clinical sites.
Work Schedule: Standard (Mon-Fri)
Job Description: Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last five years.
As part of our global team, you'll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process.
As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.).
Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.
You will ensure audit readiness and develop collaborative relationships with investigational sites.
Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.
As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process.
As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.).
Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.
You will ensure audit readiness and develop collaborative relationships with investigational sites.
Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.
Bachelor's degree in a life science related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship.
Valid driver's license where applicable.
1-2 years of traveling on-site monitoring experience is required.
Oncology, Ophthalmology, Neurology, Cardiology, Rare Disease, Respiratory, Obesity, and/or Pulmonary.
Candidates must live within 60 miles of the nearest major airport. Up to 80% travel is expected.
Must be legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check, including a drug screening.
Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals. May also include extended overnight stays.
Exposure to biological fluids with potential exposure to infectious organisms.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions
Compensation and Benefits
The salary range estimated for this position based in California is $80,000.00–$125,000.00.
https://jobs.thermofisher.com/global/en/total-rewards [https://jobs.thermofisher.com/global/en/total-rewards]
Market context
In California, experienced CRA roles are often in demand because sponsors and CROs need monitors who can travel, work across therapeutic areas, and stay current with ICH-GCP expectations. These positions are competitive because employers usually look for prior oncology or ophthalmology monitoring experience, a valid driver’s license, and the ability to handle multi-site responsibilities. Review the AI-summarized requirements and benefits here to save time, then tailor your application to highlight travel monitoring experience and therapeutic-area fit.
Research Pharmacist (Per-Diem)
Medical Lab Scientist/MT II
Study Team Associate (Per Diem)