- AbbVie (Mettawa, IL)
- …years of experience for an AD equivalent . Demonstrated success in an event coordinator 's role in the pharmaceutical industry . Project management certification ... Atogepant, BOTOX and Ubrogepant strategies (oUS) and integrated with wider event activities and communications planned by International Brand Teams within… more
- HCA Healthcare (Bradenton, FL)
- …**Introduction** Do you have the career opportunities as a(an) Pharmacy Clinical Coordinator - Pharmacist you want with your current employer? We have an ... child, elder and pet care, home and auto repair, event planning and more + Consumer discounts through Abenity...Do you want to work as a(an) Pharmacy Clinical Coordinator - Pharmacist where your passion for creating positive… more
- GAP Solutions Inc (Bethesda, MD)
- Position Objective: Provide services as a Clinical Research Coordinator in support of the overall functions of the National Institute of Neurological Disorders and ... National Institutes of Health (NIH). The primary role for this Research Coordinator (RC) position is to provide clinical research coordination and protocol… more
- Kelly Services (Kansas City, MO)
- **Clinical Research Coordinator ** + Opportunity: Temp to potential permanent employment + Location: Onsite in KS, MO + Length: No end date and goal is to convert to ... Science and Clinical is currently hiring a Clinical Research Coordinator for one of our clients who supports biotechnology...database in a timely and accurate manner. + **Adverse event monitoring and reporting** : Responsible for monitoring study… more
- Insight Global (Pennsauken, NJ)
- …trials to the people at their local pharmacy. The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of ... * Solicit and record information regarding safety events and preparing safety event documentation for review by the Principal Investigator * Provides accurate and… more
- ICON Clinical Research (Salisbury, NC)
- …be helping shape an industry. **The Role** **Title** : _Clinical Research Coordinator I_ **_Location_** _: Salisbury, NC_ **Summary:** The Clinical Research ... Coordinator I will ensure the safety of our volunteers....our mission statement + Prepares study documentation in the event of a PMG, sponsor, or FDA audit and… more
- ICON Clinical Research (Rocky Mount, NC)
- …ensures what we do, we do well. **Title: CRC Level I (Clinical Research Coordinator )** **Location: On-Site Rocky Mt NC** **Summary:** _The CRC ensures the safety of ... the investigator. + Attending investigator meetings, site initiation visits, and coordinator meetings to obtain training on drug preparation and administration and… more
- United Therapeutics (Eden Prairie, MN)
- …the planning of, preparing materials for, and presenting at investigator and coordinator meetings * Assist with study protocol training for investigators and ... such as subject screening and enrollment, data collection, and adverse event documentation * Coordinate, schedule, and conduct monitoring visits at investigational… more
- RWJBarnabas Health (New Brunswick, NJ)
- …Wood Johnson Place, New Brunswick, NJ 08901 Job Overview: The Program Coordinator provides administrative support to the Pharmacy department. Serves as the pharmacy ... training including right-to- know and laboratory training in the event of a spill will be provided and documented...including right to know and laboratory training in the event of a spill will be provided and documented… more
- J&J Family of Companies (Columbus, OH)
- …on GCPs, protocols, amendments, database, compliance, device accountability, adverse event reporting, regulatory documentation requirements + Train and proctor new ... **Preferred:** + Clinical research certification (ACRP or SoCRA, Clinical Coordinator /CRA certification) For US applicants, in accordance with applicable disclosure… more
- Edwards Lifesciences (Columbus, OH)
- …on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation ... heart anatomy + Clinical research certification (ACRP or SOCRA, Clinical Coordinator /CRA certification) + Prior clinical research experience with Class III Medical… more
- Edwards Lifesciences (Columbus, OH)
- …on GCPs, protocols, database, compliance, device accountability, adverse event reporting, study investigation protocols, amendments, regulatory documentation ... heart anatomy + Clinical research certification (ACRP or SOCRA, Clinical Coordinator /CRA certification) + Prior clinical research experience with Class III Medical… more
- Actalent (Foster City, CA)
- …for clinical and commercial projects. * Leads quality investigations/deviations/quality event escalation meetings, and effectively communicates and escalates major ... and process improvements. * May conduct or serve as a lead/ coordinator of investigations and corrective and preventive action (CAPA) recommendations related… more
- HCA Healthcare (Georgetown, TX)
- …+ Referral services for child, elder and pet care, home and auto repair, event planning and more + Consumer discounts through Abenity and Consumer Discounts + ... or university; PharmD preferred + Minimum of 1 year as a Pharmacy Clinical Coordinator OR Clinical/Operations Specialist OR one of the following: At least 5 years of… more
- PCI Pharma Services (Philadelphia, PA)
- …etc.) as needed. Support Root Cause Analysis as needed. Write quality event notifications for issues encountered on the production floor. Ensure 5s Compliance. ... Must be dependable in work attendance. May perform duties of Quality Coordinator Special Demands: The physical demands described here are representative of those… more