Location: West Region — CA, NV, CO, AZ
Contract: 6 months, potential conversion
Travel: ~8–10 days/month; regional travel primarily, occasional out-of-region travel; up to ~200 miles one way.
80 - 85% Travel Involved
Must-Haves
• 2+ years of recent ON-SITE clinical monitoring experiencePrimarily remote monitoring is not acceptable.
• If on-site monitoring was 6+ months ago, discuss further.
• Primary Monitor / Lead CRA experienceMust have independently owned sites and monitoring deliverables/reporting.
• Secondary/accompanying CRA experience does not meet the requirement.
• Large/established CRO experienceStrong preference for CRO backgrounds; pharma-only candidates should not be prioritized initially.
• Bachelor’s degree in Life Sciences preferred/expected.
• Comfortable with frequent travel by air, train, and car.
• Experience with IMVs strongly preferred.
• Experience across multiple clinical systems/EDCs such as Veeva, Medidata, Siebel, etc.
Therapeutic Experience
Strong preference: Oncology
Also valuable:
• Ophthalmology
• Neurology
• Rare Disease
• Other diverse therapeutic areas
Candidates with strong monitoring experience outside oncology can still be considered.
Visit Types
Look for experience with:
• IMV – Interim Monitoring Visits
• SIV – Site Initiation Visits
• COV – Close-Out Visits
• Evaluation/qualification visits
Important: SIV experience alone is not a rejection point, but candidates should have solid overall monitoring experience.
EEO:- Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans