Top 58 Clinical research coordinator Jobs in Nashville, Tn

Clinical Research Coordinator I
Meharry Medical College —Nashville, TN
- Full-time
- CPR Certification
- Computer literacy
- BLS Certification
21h
Clinical Research Coordinator
DelRicht Research —Nashville, TN
- $60,000 - $67,000 a year
- Full-time
- RN License
- Customer service
- Bachelor of Science
- Profit sharing
- Disability insurance
21h
Clinical Research Coordinator (CRC)
Urology Associates, PC —Nashville, TN
- Urgently hiring
- CPR Certification
- Nursing
- Vital signs
- Profit sharing
- Health savings account
Quick Apply
Clinical Research Coordinator II - Hematology/Oncology (Term Position)
Vanderbilt Health —Nashville, TN
- Part-time
- Mid-level
- Bachelor's degree
- Continuous improvement
- Health insurance
1d
Clinical Research Coordinator II
Meharry Medical College —Nashville, TN
- Full-time
- Computer literacy
- HIPAA
- Mid-level
Clinical Research Coordinator, Aesthetic Medicine
Brian Biesman, M.D. —Nashville, TN
- $60,000 - $65,000 a year
- Full-time
- Nursing
- Vital signs
- Mid-level
- Opportunities for advancement
- Referral program
Quick Apply
1d
Administrative Coordinator, Clinical Affairs
Vanderbilt University —Nashville, TN
- Full-time
- 5 years
- Mid-level
- Databases
Clinical Research Coordinator
CLINICAL TRIALS CENTER OF MIDDLE T —Franklin, TN
- 8 hour shift
- Mid-level
- Bachelor's degree
- Communication skills
- Health insurance
- Dental insurance
Quick Apply
Talent Network- Clinical Research*
Profound Research —Nashville, TN
- Hybrid work
- Clinic
- Entry level
- Health insurance
- Paid time off
Quick Apply
Clinical Research Coordinator III
Vanderbilt Health —Nashville, TN
- Full-time
- Hybrid work
- Spanish
- Bachelor's degree
- Continuous improvement
- Health insurance
Clinical Research Regulatory & Study Start-Up Coordinator
Urology Associates, PC —Nashville, TN
- Full-time
- Nursing
- Microsoft Excel
- Microsoft Outlook
- Profit sharing
- Health savings account
Quick Apply
Research Area Coordinator
Vanderbilt University —Nashville, TN
- Full-time
- Mid-level
- University
- Bachelor's degree
Labor and Delivery Clinical Nurse Coordinator
TriStar Hendersonville Medical Center —Hendersonville, TN
- Full-time
- Mid-level
- Leadership
- 2 years
- Employee stock purchase plan
- Disability insurance
Quick Apply
Clinical Coordinator
Meharry Medical College —Nashville, TN
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
4d
Clinical Coordinator
Main Street Health —Nashville, TN
- Nursing
- Microsoft Outlook
- RN License
Quick Apply
6d
Clinical Research Coordinator II
Tennessee Oncology —Gallatin, TN
- Full-time
- Spanish
- Microsoft Excel
- English
Quick Apply
Research Administrative Coordinator
OneOncology —Nashville, TN
- Full-time
- Microsoft Excel
- Mid-level
- Bachelor's degree
Quick Apply
16h
Sleep Tech Research Coordinator
Vanderbilt Health —Nashville, TN
- Full-time
- Surgery
- Mid-level
- Bachelor's degree
- Health insurance
Research Regulatory Coordinator
Tennessee Oncology —Nashville, TN
- Full-time
- Microsoft Excel
- HIPAA
- Mid-level
Quick Apply
Sr. Manager of Clinical Research Services
McKesson —Nashville, TN
- Nursing
- RN License
- Organizational skills

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Clinical Research Coordinator I

Meharry Medical College -
Nashville, TN

Apply Now

Job Details

Full-time
21 hours ago

Qualifications

Computer operation
Direct patient care
Bachelor's degree
Clinical data entry
Computer skills

Full Job Description

The Clinical Research Coordinator I (CRC I) will be responsible for specimen collection, processing, shipping, and tracking for T4C initiative. The CRC I will be responsible for inventory and keeping the lab clean and orderly at all times. He/she will use lab equipment and supplies according to standard biosafety guidelines, study protocols and Meharry regulations. Independently able to access regulations governing the protection of human subjects- IRB, FDA, OHRP, GCP/ICH and HIPAA guidelines and apply regulations in practice.

Job Description

Essential Functions (Principal Duties and Job Responsibilities):

Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses.
Maintain required records of study activity including case report forms, consenting research subjects, or regulatory forms.
Performs standard accounting functions, monitors and reviews accounting and related system reports for accuracy and completeness; prepares and reviews budget, revenue, expenses, invoices, and other accounting documents. Assist with reviews, analyzes and negotiates lab research budgets and contracts with sponsors under the direction of the Principal Investigator and Associate Director.
Performs specific protocol procedures such as interviewing subjects, taking vital signs, and performing venipunctures. Direct the requisition, collection, labeling, storage, or shipment of specimens.
Monitors study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
Schedules subjects for appointments and procedures as required by study protocols. Informs patients or caregivers about study aspects and outcomes to be expected.
Assists with preparing IRB submissions, protocol revisions, and renewals as needed, and maintains copies of all IRB communications delegated by the Principal Investigator.
Performs other related duties as assigned.

Knowledge, Skills and Abilities Required:

Must possess a good working knowledge of basic clinical research practices.
Must be proficient with personal computer.
Ability to utilize keen judgment in evaluating information.
Ability to numerically and accurately enter and calculate test results in an electronic database.
Ability to work in a stressful environment.
Must be team oriented.
Accepts constructive criticism without issues.

Knowledge, Skills, Abilities Preferred:

Knowledge of biospecimen collection, processing, labeling, aliquoting, storage, and shipment
Knowledge of biobanking principles and specimen chain-of-custody procedures
Familiarity with clinical laboratory operations and quality assurance practices
Understanding of human subject protection regulations, HIPAA, and FDA regulations
Familiarity with Laboratory Information Management Systems (LIMS)
Experience handling blood, urine, saliva, and other human biological specimens
Knowledge of centrifugation, pipetting, specimen processing, freezer inventory management, and cold-chain requirements

Education and Experience Required:

Graduated from an accredited discipline specific program and licensed as phlebotomist/lab technician in the state of Tennessee. 60 months experience in a patient care or research setting required (clinical research experience preferred).
A Bachelor’s degree in a healthcare related field. Licensed phlebotomist preferred.

Education and Experience Preferred:

One (1) to two (2) years of experience in clinical research, translational research, or biomedical laboratory research
Experience processing and handling human biological specimens
Experience supporting observational studies, clinical trials, or biobank research
Experience with specimen shipping in accordance with IATA regulations
Experience with freezer inventory management and temperature monitoring systems
Experience with REDCap, electronic medical records (EMR), CTMS, or laboratory information systems

Licensure, Certification or Registration Required:

Current Basic Life Support (BLS) certification (or ability to obtain within 90 days of hire)
Completion of Human Subjects Protection & Good Clinical Practice (GCP) training within 30 days of hire
Completion of required institutional compliance training (e.g., HIPAA, OSHA, Bloodborne Pathogens)

Licensure, Certification or Registration Preferred:

IATA Dangerous Goods Shipping Certification
Current CPR/BLS certification
Venipuncture certification or documented competency in specimen collection

Equal Employment Opportunity Statement

Meharry Medical College complies with Title IX and is an affirmative action employer. Candidates will be considered for employment without discrimination for an non-merit reason such as race, color, national origin, sex, religion, age, handicap or veteran status.

***This position is funded through a grant and is contingent upon the availability of grant funding. Employment in this role is expected to continue for the duration of the grant period, subject to satisfactory performance and the continued availability of funding. While the organization intends to maintain this position for the full grant term, employment may end or be modified if grant funding is reduced, discontinued, or otherwise unavailable.

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Refine Your Search

clinical research coordinator jobs in nashville, tn

Clinical Research Coordinator I

Clinical Research Coordinator

Clinical Research Coordinator (CRC)

Clinical Research Coordinator II - Hematology/Oncology (Term Position)

Clinical Research Coordinator II

Clinical Research Coordinator, Aesthetic Medicine

Administrative Coordinator, Clinical Affairs

Clinical Research Coordinator

Talent Network- Clinical Research*

Clinical Research Coordinator III

Clinical Research Regulatory & Study Start-Up Coordinator

Research Area Coordinator

Labor and Delivery Clinical Nurse Coordinator

Clinical Coordinator

Clinical Coordinator

Clinical Research Coordinator II

Research Administrative Coordinator

Sleep Tech Research Coordinator

Research Regulatory Coordinator

Sr. Manager of Clinical Research Services

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