Milpitas, California13 days ago
Prepare and/or review documents for submission/ essential study start-up as they relate to the assigned clinical/ performance evaluation studies (Clinical/ Performance study protocols, Informed Consent form, Investigator Brochure, Monitoring Plan, Laboratory Manual, Clinical Site Procedures, Manual, Case Report Form (CRFs), CRF Completion Guidelines and other relevant documents) in accordance with GPC, and applicable international and regional/ country practices for privacy and protection of human subjects. Waters collaborates with analytical laboratories around the world to advance the release of effective, high-quality medicines, assure the safety of food and water, and drive better patient outcomes by detecting diseases earlier, managing routine infections, and combatting growing antibiotic resistance.