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Arcetyp LLC · 9 hours ago

Clinical Research Coordinator On-site in Okinawa, Japan

San Diego, California, United States

Full-time

Onsite

Entry, Mid Level

2+ years exp

Arcetyp LLC is a growing small business that provides a broad range of consulting services to US Federal Government, US Military, and Commercial clients. They are looking for a Clinical Research Coordinator to coordinate and participate in clinical research studies, ensuring proper data collection and analysis.

Business DevelopmentConsultingInformation TechnologyProfessional ServicesProject Management

No H1B

Security Clearance Required

U.S. Citizen Only

Responsibilities

Coordinates and participates in clinical research studies by performing a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data

Coordinates and implements procedures for data collection from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources

Assists in the determination of guidelines for the collection of clinical data or administration of clinical studies

Qualification

Clinical Research CoordinationClinical MonitoringMedical TerminologyData Collection ProceduresMicrosoft Office SuiteAnalytical SkillsResearch Subject Protection TrainingSecurity ClearanceEffective CommunicationOrganizational SkillsTeamwork

Required

Bachelor's Degree from an accredited college or university and a minimum experience of 2 years as a Clinical Research Coordinator within the past five years OR current certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), OR Certified Clinical Research Professional (CCRP) from the Association of Clinical Research Professionals (ACRP) OR the Society of Clinical Research Associates (SoCRA)

Minimum of 2 to 4 years of monitoring experience in a clinical research environment and administrative Institutional Review Board (IRB) experience

Possess knowledge of medical terminology and clinical monitoring process and in depth therapeutic and protocol knowledge

Ability to communicate effectively, both orally and in writing

Possess effective organizational and analytical skills with ability to work independently and in a team environment

Proficiency with Windows base computer systems, including Microsoft Windows and Microsoft Office Suites program

Candidate must possess active/current secret security clearance

Must possess the ability to complete research subject protection training developed by the Collaborative Institutional Training Initiative (CITTI), and additional protocol specific training, as required, within one month from start date

U.S Citizenship