Clinical Research Coordinator
Company: Gulf Coast Regional Blood Center
Location: Houston
Posted on: January 26, 2023
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Job Description:
Position Title: Clinical Research Coordinator Location 1: Blood
Center Headquarters (La Concha) Hours per week: 40 Work week: 8am
to 5pm Shift: Monday through Friday Driving position: No
Description: GULF COAST REGIONAL BLOOD CENTERLocation: 1400 La
Concha Lane in Houston, Texas 77054 Position Title: Clinical
Research Coordinator Function Titles: Clinical Research Associate,
Clinical Researcher, Cellular Life Coordinator Join our team of
heroes!Gulf Coast Regional Blood Center has an exciting opening for
a Clinical Research Coordinator! Reporting to the Cellular Life
Solutions' Director, and under direct supervision of Chief Medical
Officer/Assoc. Vice President of Medical Services, the Clinical
Research Coordinator (CRC) serves to lead in the coordination,
management and initiation of collection products involved in a
client's clinical research trial. This individual will be directly
involved with vetting and evaluating potential clients, overseeing
paperwork. They will also assist the investigating
physician(s)/Principal Investigator(s) (PIs) with the preparation
of regulatory documents, planning, subject recruitment, enrollment,
and study conduct for complex various protocols. The CRC will train
and mentor health care personnel on protocols and ensure correct
adherence under the direction of the PI. This includes both GCRBC
institutional studies, client specific protocols/studies, and
multi-institutional consortium-sponsored trials. JUST FOR YOU:
Competitive compensation and benefits package.Texas Medical Center
location with free parking. Work-life Balance: No on-call or
weekend schedule. Engaging and exciting opportunity to SAVE LIVES.
Tips to thrive in our culture:Embody our Core Values of Commitment,
Integrity, and RespectWork to actively create experiences that
inspire others to save lives, each and every day.Embrace doing it
right, making connections, and creating desired experiences.Comply
with all organizational policies and standards, including safety
rules, and be willing to report actual and potential violations to
the appropriate supervisor or manager. In this role,
you'll:Maintain working knowledge of the research process and the
conduct of IRB approved research protocols. Follow and enforce
ICH/GCP/GTP/GMP guidelines. Manage information gathering for
vetting and evaluation of potential clients, budget preparation,
and execution of appropriate protocol/study requirements for new
client onboarding processUnder the direction of Medical Director,
conduct screening and interviews to evaluate patient and/or donor
eligibility in studyPrepares and participate in audits conducted by
protocol personnel.Maintains the theoretical and procedural
knowledge necessary to preform and interpret assigned procedures
performed within the Laboratory. Respond promptly and accurately to
customer complaints, inquiries, and requests for information,
coordinate appropriate follow-up calls and/or appointmentsMaintain
records for clinical study and regulatory documents.Attend meetings
as required. Initiate project management charters as neededAssists
with donor recruitment/scheduling as neededAssists with
revision/creation of SOPsPerform other reasonably related
business/job duties as assigned. GCRBC reserves the right to revise
job duties and responsibilities as the need arises.Assist with
oversight of IRB documents, notifications, updates and
submissionsComplete additional duties as assigned. We need someone
who has:Bachelor's Degree (BS) from an accredited college or
university in Biology or Chemistry with a minimum of one-year
related experience in clinical or research laboratory/clinical
setting.Certification as a Clinical Research Coordinator (CCRC or
CCRP) preferred.Sufficient proficiency in speaking, reading, and
writing the English language necessary to perform the essential
functions of this job, especially with regard to activities
impacting patient, donor or employee safety or security.Attention
to detail, focus on accuracy. Think you have what it takes to save
lives with us? We want to hear from you! EQUAL OPPORTUNITY EMPLOYER
STATEMENTThe Blood Center is an Affirmative Action/Equal Employment
Opportunity Employer. Qualified applicants for positions are
considered without regard to race/ethnicity, color, religion,
national origin, age, pregnancy, sex, sexual orientation, gender
identity, transgender status, military status, protected veteran
status, disability status, genetic testing results or any other
basis or characteristic prohibited by applicable law, statute,
regulation or Executive Order. PI202071792
Keywords: Gulf Coast Regional Blood Center, Houston , Clinical Research Coordinator, Healthcare , Houston, Texas
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