Sub-Investigator
On-siteSan Antonio, Texas, United States
San Antonio, Texas, United StatesOn-siteFull Time
Full Time
Job Summary
Conduct follow-up visits, review labs, and coordinate treatment for study subjects while performing physical examinations, informed consents, and vital sign collections. Recruit participants into protocols and screen candidates, maintaining strict confidentiality and adhering to FDA regulations, GCP, and IRB policies. Collaborate with affiliates, internal staff, and industry sponsors to prepare for monitor visits and manage multiple projects with competing priorities. Requires bilingual English/Spanish proficiency and a current advanced registered nurse practitioner or physician assistant license.
Required Qualifications
- Advance degree from a graduate school
- one to two years related experience and/or training
- equivalent combination of education and experience
- Specialized training
- Current advanced registered nurse practitioner or physician assistant license
- Valid driver's License
- Bilingual (English/Spanish)
- Written and oral communication skills
- Organizational skills
- Ability to pay attention to detail
- People skills including possessing a positive, friendly, and professional demeanor
- Ability to be flexible with changing priorities
- Ability to communicate in a diplomatic and professional manner
- Strong interpersonal skills
- Strong mathematical knowledge
- Excellent computer skills
- Knowledge of Microsoft Office, Internet Explorer, Google Chrome, Mozilla Foxfire, and web-based enterprise solutions software
- Occasional travel may be required domestic and/or international
- Ability to work in an upright and/or stationary position for 6-10 hours per day
- Frequent mobility required
- Occasional squatting, kneeling, or bending
- Light to moderate lifting and carrying (or otherwise moves) objects including medical equipment with a maximum lift of 20-50 lbs
Desired Qualifications
- GCP Training certification preferred
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