Clinical Research Coordinator
Company: Allergy A.R.T.S.
Location: Amarillo
Posted on: May 11, 2022
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Job Description:
Job Description Salary: Clinical Research Coordinator Job
Summary The Clinical Research Coordinator (CRC) is a specialized
research professional working with and under the direction of the
Research Director and clinical Principal Investigator (Pl). While
the Principal Investigator is primarily responsible for the overall
design, conduct, and management of the clinical trial, the CRC
supports, facilitates, and coordinates the daily clinical trial
activities and plays a critical role in the conduct of the study.
By performing these duties, the CRC works with the PI, department,
sponsor, and institution to support and provide guidance on the
administration of the compliance, and other aspects of the clinical
study. Essential Responsibilities: Responsible for ensuring all FDA
and GCP guidelines are strictly adhered to and follow all Standard
Operating Procedures for ACCR Plan and coordinate the initiation of
research study protocol Plan, implement, and maintain data
collection and analysis systems in support of research protocol
Recruit, instruct, and coordinate research subjects, as appropriate
to specific study objectives and work scope. Must be able to screen
patient charts, and have the critical thinking skills necessary to
make independent decisions based on outlined screening
qualifications each study presents. The expectation is minimum of
one patient screened in clinic per study for average job
performance. Responsible for all recruitment and retention for
assigned protocol. Communicate enrollment barriers immediately to
Director. Create and maintain weekly screening log for all assigned
studies. Answer phones and direct calls to the appropriate
individual Responsible for hands on patient care, including rooming
subjects, vital signs, EKG's, lab draws, processing specimens, and
other clinical tests as needed. Maintain lab supply for all visits
required by protocol. Create source documents as needed for
individual studies Data entry of completed source docs within a
maximum of 5 days unless otherwise dictated by sponsor/CRO. Query
resolution within 3 days for all assigned studies. Attend
Investigator, site initiation and other training meetings as
necessary Organizing regulatory files and filing all documents in
study files 48 hours prior to any sponsor/CRA visit Obtain all
required signatures within 5 business days Conduct weekly check ins
with clinic staff about current studies Obtain thorough medical
histories for all possible subjects Qualifications Education: High
School Diploma required; Bachelor---s/Master---s preferred Clinical
Research Experience: Preferred, but not required Knowledge of
medical terminology : Required Ability to read, write, and
understand medical terminology Ability to effectively organize
files, meet deadlines, write routine documents, speak clearly, and
solve practical problems Ability to complete tasks autonomously and
take initiative to complete their work Ability to work with others
in a wide variety of circumstances Ability to work with diverse
groups of people Language Skills Must have the ability to read,
analyze, and interpret complex documents, respond effectively to
sensitive inquiries or complaints. Clearances Criminal Background
Check TB Clearance Hep B Clearance Testing Pre-employment drug
testing Physical Demands While performing the duties for this job,
the employee is occasionally required to stand, walk, and sit for
long periods of time. The employee must occasionally lift up to
25lbs. Salary Commensurate with experience
Keywords: Allergy A.R.T.S., Amarillo , Clinical Research Coordinator, Healthcare , Amarillo, Texas
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