Job Description
NRC Research Institute has been conducting clinical trials for the world’s pharmaceutical firms since 2004. We specialize in pharmaceutical clinical trials involving CNS (Central Nervous System) disorders such as Schizophrenia, Bipolar Disorder, Depression, ADHD, Autism, and more. We are looking for an energetic entry-level Clinical Research Coordinator (CRC) to join our team.
The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring a high level of knowledge of study specific protocols, as well as coordination and collaboration with research colleagues and departments.
Job Duties:
• Perform study procedures in accordance with GCP and study protocols
• Coordinate protocol related research procedures, study visits, and follow-up care
• Organize and maintain paper and electronic study data in a complete and correct manner
• Work closely with recruitment and prescreening teams to meet study enrollment goals
• Adhere to an IRB approved protocol
• Participate in the informed consent process of study subjects
• Support the safety of clinical research patients/research participants
• Maintain study source documents
• Report adverse events
• Educate subjects and family on the protocol, study intervention, study drug, etc.
• Comply with Institutional policies, standard operating procedures (SOPs) and guidelines
• Complete case report forms (paper & electronic data capture) and address queries
• Facilitate study initiation, monitoring visits, and close out activities
• Retain records/archive documents after study close out
• Requires effective writing and communication, work as part of a team, ability to multitask
• Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals
• Document investigational product (drug/device) accountability
Qualifications:
Compensation:
min $25/hr DOE
Health, dental, and vision insurance, 401(k), and other benefits are available for eligible full-time employees.
This is a full-time onsite position (40 hrs/week). Hours are Mon-Fri, 8:30 am - 5:00 pm
...The Department of CT Surgery seeks an LVAD Coordinator to join their team. In collaboration with physicians and multidisciplinary... ...patients and families requiring mechanical cardiac assistance and transplantation. Responsibilities include: Coordinate and...
Job Description Job Description Kia Retailers are offering skilled and experienced military Veterans with the opportunity to begin an inspiring career as a Kia Certified Service Technician. To support this Kia Retailer initiative, Kia America, Inc. has established ...
...products Required: ~ Excellent written and verbal communication skills, passion for teaching and coaching ~ Self-starting team player who thrives in an agile fast-paced environment (With minimal direction)~3+ years in a manufacturing training role with...
Alliance Highway Safety - Marketing and Events InternshipAlliance Highway Safety is looking for FUN, ENERGETIC, OUTGOING individuals to help coordinate a variety of sponsorship events across the country. As part of Alliance's internship program, you will have the opportunity...
...Description RemX is looking for Customer Service Reps. This is a short term ONSITE project either in Miramar or Plantation, FL. Title: Temp Customer Service Representative Location: Onsite ( Plantation or Miramar, FL) Pay: $17/hour $18/hour for bilingual...