Job Description

Job Description

Job Description

NRC Research Institute has been conducting clinical trials for the worlds 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:

Regular travel between multiple sites in LA/OC area expected
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:

Bachelors Degree required; degree in Biology and/or Psychology field preferred
Must be willing and able to work in a clinical setting involving a psychiatric/mentally disabled population
Must have ability to read and understand clinical trial protocols
Must have attention to detail and the ability to handle multiple tasks with precision
Must be adept with computers
Must possess excellent critical thinking skill
Must have excellent interpersonal and communication skills and be a hardworking team player
Must possess strong data management skills
Familiarity with medical terminology/environment required

Compensation:
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, 8:00 am - 4:30 pm

Job Tags

Full time,

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