Clinical Research Associate

Job Description...

• Responsible for overall clinical study management, including planning, communication, coordination and practical tasks for the studies.
• Coordinates Ethical Committee and Institutional Review Board notifications.
• Creates, maintains and oversees study files and archiving.
• Manages testing laboratories including selection of laboratories for the studies.
• Manages clinical research organizations and ensures monitoring of studies, data collection and handling.
• Prepares, revises and maintains procedures for the conducting of clinical studies.
• Bachelor's or Master's Degree or equivalent.
• Post-graduate, certification, and / or license may be required.
• Typically, at least 3 - 5+ years relevant experience.

EEO Employer

LanceSoft is a certified Minority Business Enterprise (MBE) and an equal opportunity employer. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. LanceSoft makes hiring decisions based solely on qualifications, merit, and business needs at the time.