Clinical Research Associate II / Sr. CRA, West Coast US
$90,000–$140,000 year
RemoteUnited States
United StatesRemoteFull Time$90,000–$140,000 yearMid LevelBachelors DegreeMedium
Full TimeMid LevelBachelors DegreeMedium
Job Summary
Conduct all site monitoring visit activities including PSV, SIV, IMV, and COV, while participating in site selection and managing required documentation to ensure audit readiness. Provide feedback to sites for resolving deficiencies, contribute to protocol and study tool development, and mentor junior team members. Perform both onsite and remote monitoring and study closure across multiple protocols, attending investigator meetings and the RFP process. Maintain effective relationships with clinical sites and internal teams to communicate project goals.
Required Qualifications
- BA/BS, preferably in a life science, nursing, pharmacy or related field
- approximately 2 years (CRA II) or 4-5 years+ (Senior CRA) of on-site monitoring experience within the CRO, pharmaceutical, or biotechnology industry
- demonstrated understanding of medical/therapeutic area knowledge and medical terminology
- Computer literacy, including proficiency in MS Office and use of EDC systems
- Demonstrate written, verbal and presentation skills
- attention to detail
- deep understanding of our high-quality scientific standards
- ability to care about every outcome
- strong organization skills
- effective management of multiple sites and protocols within timeframes and on budgets
- Contribute to our collaborative culture with honesty and integrity
- willingness to learn and train
- strong team spirit highlighted by loyalty, accountability, and mutual trust
- ability to change quickly
- 8-10 site visits days per month (up to 80% travel)
- remote role to be located within a 1-hour commute of a US metropolitan airport
Desired Qualifications
- Master's degree
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