Top 3 Cra Jobs in Columbus

Clinical Research Coordinator I - RI Biobeh Fox
Nationwide Children's Hospital —Columbus, OH
- Weekends as needed
- Word processing
- Writing skills
- Analysis skills
6d
Clinical Research Assistant - Comprehensive Cancer Center
The Ohio State University Wexner Medical Center —Columbus, OH
- Online Application
- Background check
- Pass drug screening
- Mid-level
4d
Clinical Research Coordinator I - RI Behav Trials Off
Nationwide Children's Hospital —Columbus, OH
- Weekends as needed
- Hospital
- Word processing
- Writing skills

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Clinical Research Coordinator I - RI Biobeh Fox
Nationwide Children's Hospital —Columbus, OH
Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…
6d
Clinical Research Assistant - Comprehensive Cancer Center
The Ohio State University Wexner Medical Center —Columbus, OH
Bachelor's degree in biological or social sciences or an equivalent combination of education and experience required; 2-4 years experience in a clinical…
4d

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Clinical Research Coordinator I - RI Biobeh Fox

Nationwide Children's Hospital -
Columbus, OH

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Job Details

Full-time
6 days ago

Qualifications

Record keeping
Regulatory documents
Informed consent
Research ethical considerations
Phone communication
Word processing
Writing skills
Patient advocacy
Phlebotomy specimen handling
State healthcare regulations
Patient safety
Medical scheduling
Research project coordination
Analysis skills
ICH guidelines
Interview research
Clinical data entry
Data management
Decision making
Laboratory standard operating procedures
Informed consent procedures implementation
Medical laboratory work experience
CLIA regulations
Research compliance clinical trial records management
Clinical trial standard operating procedures
Adolescents
Clinical trial patient safety management
Implementing research protocols
Patient recruitment
LPN

Full Job Description

Overview:

Dr. Kristen Fox seeks a Clinical Research Coordinator to join her research program focused on health behaviors, psychosocial functioning, and healthcare experiences of youth with congenital heart disease. The coordinator will support a randomized clinical trial evaluating a digital health intervention and other research. Responsibilities include obtaining informed consent/assent from adolescents and adults by phone or in person, coordinating and scheduling research activities, managing data, and assisting with qualitative interviews. This position requires in-person work. During active recruitment and data collection, flexibility to work approximately 4 hours/week during evenings and weekends is required to accommodate family schedules. The position is available immediately.

Job Description Summary:

Manages elements of a clinical study in order to meet all protocol obligations while following ICH/GCP guidelines; and departmental/institutional standard operating procedures. These elements include but are not limited to; start-up activities, launch activities, day to day management of a study and study closure activities.

Job Description:

Essential Functions:

Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers questions related to the protocol procedure as applicable; acts as a patient/family advocate.
Ensures that the subject meets inclusion/exclusion criteria; alerts the investigator when the subject’s safety is in jeopardy, there is a protocol deviation, or when the subject requests premature study termination.
Collects and manages research data and subject information; and maintains accurate data collection of all study data; including laboratory analytical procedures.
Prepares and processes human specimens for use in research studies. Collects blood, urine, and other samples as needed according to skill level and certifications. Performs CLIA waived laboratory assessments. Such activities may be performed independently and may require evening and weekend hours.
Completes screening sheets and recruitment logs.
Creates source documents that facilitate systematic data collection and/or aid in protocol execution and management and record keeping; and conducts accurate and timely subject data collection.
Collaborates, coordinates, and schedules subject study visits with other hospital services and the PI/sub-I.
Adheres to departmental quality control guidelines.
Completes Case Report Forms (CRFs) as instructed by the sponsor; ensures CRF’s are completed prior to monitoring visits.
Maintains regulatory binder and documents.

Education Requirement:

Associate's Degree, or equivalent certification or experience, required.
Bachelor's Degree, preferred.

Certifications:

CNA, PCA, LPN, MA, or equivalent education or experience, required.
Clinical Research Associate (CRA) or Clinical Research Coordinator (CRC) certification after hire, required.

Skills:

Understanding of medical terminology and clinical research preferred.
Working knowledge of PCs and word processing and data management software
Demonstrated analytical skills with accuracy and attention to detail.
Excellent verbal and written communication skills.
Goal-oriented and self-directive
Strong organizational and interpersonal skills.
Ability to actively participate as a team player.

Experience:

Previous experience in clinical research or health care related field preferred.

Physical Requirements:

OCCASIONALLY: Cold Temperatures, Fume /Gases /Vapors, Loud Noises, Reaching above shoulder, Squat/kneel

FREQUENTLY: Bend/twist, Biohazard waste, Blood and/or Bodily Fluids, Chemicals/Medications, Communicable Diseases and/or Pathogens, Lifting / Carrying: 0-10 lbs, Lifting / Carrying: 11-20 lbs, Lifting / Carrying: 21-40 lbs, Machinery, Patient Equipment, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 26-40 lbs, Pushing / Pulling: 41-60 lbs, Pushing / Pulling: 61-100 lbs, Sitting, Standing, Walking

CONTINUOUSLY: Audible speech, Computer skills, Decision Making, Depth perception, Flexing/extending of neck, Hand use: grasping, gripping, turning, Hearing acuity, Interpreting Data, Peripheral vision, Problem solving, Repetitive hand/arm use, Seeing – Far/near

"The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individuals so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under their supervision. EOE M/F/Disability/Vet"

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cra jobs in columbus

Clinical Research Coordinator I - RI Biobeh Fox

Clinical Research Assistant - Comprehensive Cancer Center

Clinical Research Coordinator I - RI Behav Trials Off

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