- Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
- …and overseeing complex microbiological testing and environmental monitoring (EM) in compliance with cGMP, USP, FDA, and internal quality standards. This position ... QC department laboratory supplies. + Ensures laboratory equipment is in compliance with procedures and GLP requirements. + Troubleshoots laboratory issues related… more
- Beth Israel Lahey Health (Burlington, MA)
- …of all aspects of clinical trials research adhering to Research SOPs, GCP compliance and FDA regulations. 2) Functions as a mentor, resource and educator for ... and other colleagues related to Research conducted within the department. 3 ) Functions as an interdepartmental liaison, evaluating, coordinating, and facilitating… more
- Lilly (Indianapolis, IN)
- …programs. Maintain a focus on accelerating timelines while ensuring quality. + Demonstrate compliance with procedures and be accountable for compliance of team ... + Lead completion of clinical trial documents including protocols, amendments, investigator brochures, informed consent forms, and clinical study reports. +… more
- HCA Healthcare (Overland Park, KS)
- …for emotional, physical and financial wellbeing + 401(k) Plan with a 100% match on 3 % to 9% of pay (based on years of service) + Employee Stock Purchase Plan ... (https://careers.hcahealthcare.com/pages/employee-benefits-and-rewards) The **Clinical Research Coordinator (CRC)** assists the principal investigator (PI) and sub investigators with all aspects of… more
- University of Pennsylvania (Philadelphia, PA)
- …research protocols, as well as assist in the conduct of investigator -initiated research and division-specific research projects and operations. This position's ... in study team meetings, disease site group meetings, and ongoing protocol training/ compliance meetings. Supports in the monitoring of external sites and assists in… more
- US Tech Solutions (North Chicago, IL)
- …Communication Skills; providing updates across functions; written and verbally 3 . **Contractual or Paralegal** experience highly preferred **Purpose:** The Contract ... including **Clinical Study Agreements, Confidential Disclosure Agreements, Master Agreements, Investigator Initiated Agreements, Service Agreements** ect In partnership with… more
- University of Colorado (Aurora, CO)
- …#:00841365 - Requisition #:38121** **Job Summary:** **Key Responsibilities:** + Ensures compliance with each study's protocol by providing thorough review and ... proper medication dosage, administration, and disease treatment. + Ensures site compliance with research protocols by reviewing all regulatory requirements to… more
- University of Utah (Salt Lake City, UT)
- …develops and coordinates the submission of regulatory documents to ensure compliance with governing requirements. Oversees research study documents in an ... administrative and operational capacity while maintaining compliance with guidelines set by governing agencies. The University of Utah offers a comprehensive… more
- University of Miami (Miami, FL)
- …collection/recording, and daily operations of moderate risk clinical research protocols. 3 . Collects, processes, packs, and ships specimens according to protocol, ... standards and clinical credentials as delegated by the Principal Investigator . 6. Monitors, documents, reports, and follows-up on study unanticipated/adverse… more
- University of Colorado (Aurora, CO)
- …+ Serve as the primary clinical research coordinator for investigator -initiated and clinical research protocols. + Collaborates with investigators, clinical ... per protocol and properly documented. + Ensure protocol specific compliance and compliance with FDA, OHRP, GCP,...degree in science or health related field. + Three ( 3 ) years of clinical research or related experience. +… more