Investigator Jobs in San Antonio, TX

About The Position

Requirements

• Bachelor's degree preferred, but not required
• Phlebotomy experience is required; EKG or other patient labs/processes preferred
• Preferably 1+ year of experience as a Clinical Research Coordinator
• Familiar with e-source reporting via an electronic platform
• A clear understanding of ICH, FDA, and GCP regulations
• Impeccable organizational skills and attention to detail
• Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources
• An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven
• High-level critical thinking skills
• Working knowledge of medical terminology and lab collection/processing/storage procedures
• Proficiency with computers and Microsoft Office Suite

Responsibilities

• The Clinical Research Coordinator (CRC) obtains study participant informed consent.
• Executes study protocol procedures in a detailed, organized, and professional manner.
• Performs human specimen lab draws and processing, and packages specimen shipments.
• Creates and completes study source documents and adverse event reporting on an e-source system.
• Maintains study-specific files and supplies.
• Communicate with the Study Sponsor/CRO regarding study-specific questions.
• Participates in site visits from Sponsors/CROs, including site initiation and monitoring visits.
• Additional responsibilities as assigned by management.

Benefits

• Health, dental, and vision insurance plans
• 401(k) with a 100% employer match on the first 4% of employee contributions
• Tuition reimbursement
• Parental leave
• Referral program
• Employee assistance program
• Life insurance
• Disability insurance
• 15 days of PTO + 8 paid holidays and 2 floating holidays.