Screening Coordinator – Clinical Trials – Full Time

California Job Vacancies

Job SummaryThe role of the Screening Coordinator is to serve as an integral member of the study team overseeing and coordinating the informed consent and screening process.WCCT Global, LLC is a pharmaceutical contract research organization that offers outsourced early drug development and late phase services to pharmaceutical, biotechnology, and medical device industries worldwide.

We are proud to offer services in the areas of cardiovascular, gastrointestinal, infectious disease and vaccines, ophthalmology, respiratory, and immunology and allergy.

WCCT Global, LLC was formerly known as West Coast Clinical Trials, LLC.

We were founded in 1998 and are based in Cypress, CaliforniaPLEASE NOTE: This position requires working onsite, at our Cypress, Ca.

headquarters location; this is not a remote position.

Local candidates are preferred however, you may choose to relocate at your own expense .Essential Job Functions+ Follow all study and non-study regulations including, but not limited to: Patient/Subject Privacy (HIPAA), OSHA, Good Clinical Practice (GCP), Good Documentation Practice(GDP), Standard Operating Procedures (SOP), and department specific Work Instructions(WI)+ Follow proper safety and emergency policies and procedures as set forth by the company+ Perform basic medical front office duties, including but not limited to: welcoming study participants, answering or referring inquiries, recording and/or collecting study participant information, verifying subjects?

information update to most current, and preparing study specific charts daily+ Perform and complete study procedures, including but not limited to: vital signs, electrocardiogram, height, weight, blood collection, meal distribution, pulmonary function tests, check in/out of volunteers, etc.+ Fully execute the Informed Consent Process including but not limited to: medical history, social h istory, demographics, etc.+ Attend study-specific meetings including but not limited to: SIV, study award, planning meetings & screening trainings+ Read and understand all study-specific protocols & ICF?s.+ Maintain assigned work area in a clean and safe condition+ Monitor own work and resolve queries in a timely manner+ Review Inclusion/Exclusion Criteria and source documents for all screening visits conducted+ Ensure availability of study participant?s information by accurately filing and/or retrieving study participant records as requested by management+ Adhere to project work plans and revisions as appropriate to meet any change in needs and requirements+ Perform quality control review of completed screening sources and ensure data is present for Investigators to review and sign to determine subject eligibility+ Maintain and update all study related documents including, but not limited to: DOA?s, attendance sheets, screening logs, FAQ, etc.QualificationsEducation+ ?

High School diploma or General Education Degree (GED)
– required+ ?

3-6 months related experience and/or training, or the equivalent combination of education and experience
– requiredExperience/Training+ ?

1-2 years of working experience in Clinical Research (either as a Screening Coordinator or other position)
– required+ ?

IV/Blood withdraw experience
– preferred+ ?

Knowledge of basic medical terminology
– requiredCertifications+ ?

Current BLS certification
– required+ ?

Medical Assistant (MA) and/or CPT1 certificate
– required+ ?

LVN or higher
– preferredWCCT Global, LLC is a pharmaceutical contract research organization that offers outsourced early drug development and late phase services to pharmaceutical, biotechnology, and medical device industries worldwide.

We are proud to offer services in the areas of cardiovascular, gastrointestinal, infectious disease and vaccines, ophthalmology, respiratory, and immunology and allergy.

WCCT Global, LLC was formerly known as West Coast Clinical Trials, LLC.

We were founded in 1998 and are based in Cypress, California



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