Top 130 Clinical data coordinator Jobs in Nashville, Tn

Research Assistant
Tennessee Retina MSO LLC —Nashville, TN
- Background check
- Private practice
- Anatomy knowledge
- Health savings account
- Paid holidays
Quick Apply
Advanced Clinical Research Coordinator
TN Comprehensive Lung and Sleep Center, PC —Hendersonville, TN
- From $65,000 a year
- Full-time
- Nursing
- RN License
- Internal Medicine
- Health insurance
- Dental insurance
Quick Apply
Center-based Early Intervention ABA Paraprofessional
Ascend Autism —Nashville, TN
- $20 - $27 an hour
- Part-time
- Clinic
- Experience working with children
- Psychology
- Continuing education credits
- Dental insurance
Quick Apply
Data Coordinator
Sarah Cannon Research Institute —Nashville, TN
- Full-time
- English
- Bachelor's degree
- Entry level
Data Coordinator
McKesson —Nashville, TN
- English
- Bachelor's degree
- Entry level
Clinical Research Coordinator
TriStar Centennial Medical Center —Nashville, TN
- Full-time
- Experience equivalent to degree accepted
- 1 year
- Entry level
- Employee stock purchase plan
- Disability insurance
Quick Apply
HEALTH STARTS PROGRAM LEAD - 78823
TennCare —Nashville, TN
- $67,764 - $108,060 a year
- Full-time
- Hybrid work
- Background check
- Microsoft Excel
- Adults
- Work from home
7d
Medical Record Coordinator
Software Technology Inc —Nashville, TN
- HIPAA
- Mid-level
- Case management
Quick Apply
Central Authorization Coordinator
Work from Home —Nashville, TN
- Full-time
- Mid-level
- Analysis skills
- 1 year
- Employee stock purchase plan
- Disability insurance
Quick Apply
Medical Record Coordinator and Abstractor
Software Technology Inc —Nashville, TN
- Full-time
- Hybrid work
- HIPAA
- Mid-level
- Office
Quick Apply
Manager, Care Coordination Operations
Oshi Health —Nashville, TN
- $120,000 - $140,000 a year
- Weekends as needed
- HIPAA
- Mid-level
- Communication skills
- Paid holidays
- Health insurance
Quick Apply
4d
Senior Clinical Analyst
HCA Healthcare —Nashville, TN
- Full-time
- 5 years
- Mid-level
- Organizational skills
- Employee stock purchase plan
- Disability insurance
Quick Apply
Hospital Billing Coordinator
Deloitte —Hermitage, TN
- $50,000 - $60,000 a year
- Full-time
- Microsoft Excel
- Mid-level
- Bachelor's degree
Public Health Nursing Consultant 1
Software Technology Inc —Nashville, TN
- Full-time
- Hybrid work
- HIPAA
- Mid-level
- Office
Quick Apply
Clinical Research Coordinator III
Vanderbilt University Medical Center —Nashville, TN
- Full-time
- Hybrid work
- Spanish
- Bachelor's degree
- Continuous improvement
- Health insurance
Report Coordinator - Flow Cytology
Labcorp —Brentwood, TN
- Full-time
- Computer literacy
- Medical office experience
- Laboratory experience
- Employee stock purchase plan
- Disability insurance
12d
Biorepository Coordinator I PMI
Vanderbilt University Medical Center —Nashville, TN
- Full-time
- Bachelor of Science
- Bachelor's degree
- Perioperative Care
- Health insurance
5d
Discharge Transport EMT
Work from Home —Nashville, TN
- Full-time
- Mid-level
- Leadership
- 2 years
- Employee stock purchase plan
- Disability insurance
Quick Apply
8d
Admissions Coordinator
Apex Recovery LLC (TN) —Brentwood, TN
- Clean driving record
- Sales
- High school diploma or GED
Quick Apply
Intake Coordinator I
Acadia Healthcare —Franklin, TN
- Full-time
- Hybrid work
- Microsoft Excel
- English
- Bachelor's degree
- AD&D insurance
- Paid holidays
14d

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Research Assistant

Tennessee Retina MSO LLC -
Nashville, TN

Quick Apply

Job Details

Benefits

Health savings account
Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Uniform allowance
Employee assistance program
Vision insurance
401(k) matching

Qualifications

Report preparation
Direct patient care
Healthcare incident report preparation
Medical chart preparation
Anatomy knowledge
HIPAA compliance
Regulatory documents
Informed consent
Patient monitoring
Adverse event reporting
Copy machines
Patient demographics
HIPAA
Care documentation
Assisting medical staff
High school diploma or GED
Transcription
Schedule management
ICH guidelines
Patient history taking
Collecting samples for laboratory testing
Records management
Data management
Adverse drug reaction monitoring
Informed consent procedures implementation
Medical record retrieval
ECG placement
Research compliance clinical trial records management
Organizational skills
Clinical trial standard operating procedures

Full Job Description

Who We Are

Tennessee Retina is the largest Ophthalmology practice in middle Tennessee offering rewarding careers across 10 locations. We are committed to providing the highest level of care to our patients in the most convenient and caring manner. Our physicians are leaders in the research and application of new retina, macula, and vitreous treatments.

We are seeking an energetic and collaborative Research Assistant. The research assistant is primarily responsible for assisting in research patient visits according to ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures.

This exciting opportunity will work closely and be supported by a team of colleagues, strong leadership, and cutting-edge technology! A day in the life of a Tennessee Retina employee is filled with learning, growing, creating, hard work, and most of all fun!

Tennessee Retina offers a competitive salary based on diverse experiences and backgrounds.

Benefits Offered

Sign-On Bonus, Certification Incentive Bonus, and Length of Service Award Bonus Programs
Paid Continue Professional Education (CPE)
COA/COT exam resources and reimbursements
Tuition Reimbursements
Transportation Reimbursement Program
Employer-sponsored Medical, Dental, Vision, Critical Illness Coverage, Short-term, Long-Term Disability, & Employee Assistance Program
401(k) with Generous Employer Match
Health Savings Account (HSA) and Flexible Spending Account (FSA)
Paid Holidays and Paid Vacation
Annual Scrub Uniform Allowance
Employee Referral Award Bonus Program
Succession, Growth, and Mentorship Opportunities
Social Gathering and Team Opportunities
Full new hire training program to fully support, train, and welcome new hires to the team

Responsibilities

Review and comprehend all study protocols assigned, such as study proceedings and timelines, inclusion and exclusion criteria, confidentiality, and privacy protections.
Coordinate and schedule subject visits within study/subject-specific windows per protocol guidelines.
Prepare visit-specific documentation and charts for the Clinical Research Coordinator
Efficiently and accurately interviews patients and documents histories
Conducts and/or participates in the informed consent process/discussion with research participants, including answering any questions related to the study. Obtains appropriate signatures and dates on forms in proper places per the research SOP. Assures that amended consent forms are appropriately implemented and signed respectively.
Assist the Coordinator in patient care and management
Assist the Coordinator in monitoring subject flow and assist in subject care and management
Accurately collect and record all necessary data for follow-up, screening, and randomization study visits (e.g., demographics, medical history, adverse events, concomitant medications, etc.).
Administer all mandatory questionnaires to study subjects
Set up, prepare subject, and conduct electrocardiograms (ECG) on subjects per study protocol
Collection, processing, and shipment of laboratory biological samples for analysis
Perform intraocular pressure checks
Perform Snellen VA for specified studies
Review and resolve data management queries as needed
Scribe ocular exams for doctors and confirm appropriate treatment per protocol
Assist/perform with treatment preparation and administration (on selected studies, as assigned).
Assist the Coordinator with maintaining IP/device accountability and shipping logs (on selected studies, as assigned).
Serious Adverse Event Reporting initial & follow-up reporting, including promptly requesting all necessary medical records, review of medical records, and updated reporting
Training/Understanding all aspects of regulatory
Assist Coordinator in regulatory management, including training and monitoring visits
Assist the Coordinator in CTMS management (when available).
Transcribe and query resolution subject study information from source documents to the Electronic Case Report Form in the required timeframe.
The responsibilities listed are a general overview of the position and additional duties may be assigned.

Education, Training, and Experience

High School Diploma or the equivalent
Scribing experience preferred
Obtain and maintain any applicable additional/required sponsor training and/or certifications
Demonstrates working knowledge of eye anatomy, disease, symptoms, and ocular medications
Meticulous attention to detail is required.
Demonstrates high-level critical thinking skills
Cooperates with supervisory staff, physicians, peers, external customers, and patients in a positive, energetic, and professional manner
Effective verbal and written communication skills with patients, physicians, management, and employees
Excellent Organizational skills, multi-task, and logical thinking
Ability to be proactive, take initiative, and perform well in a fast-paced, high-volume practice.
Basic understanding of eye anatomy, medical terminology, ocular pathology, and eye diseases.

Confidentiality
Maintains strict confidentiality regarding protected health information (PHI) and understands and adheres to TNR’s HIPAA privacy and security policies and procedures.

Typical Physical and Working Demands
Position requires consistent physical activity, including prolonged walking, sitting, bending, stooping, and stretching. Excellent manual dexterity and hand-eye coordination are essential for operating a keyboard, telephone, photocopier, and specialized optical equipment. Requires the ability to frequently lift, carry, push, and pull heavy items, including optical devices weighing 15 pounds or more. Must possess standard hearing and near/far vision (corrected to normal range) to accurately prepare paper and MDI chart notes, communicate with patients, and generate reports.

Quick Apply

Refine Your Search

clinical data coordinator jobs in nashville, tn

Research Assistant

Advanced Clinical Research Coordinator

Center-based Early Intervention ABA Paraprofessional

Data Coordinator

Data Coordinator

Clinical Research Coordinator

HEALTH STARTS PROGRAM LEAD - 78823

Medical Record Coordinator

Central Authorization Coordinator

Medical Record Coordinator and Abstractor

Manager, Care Coordination Operations

Senior Clinical Analyst

Hospital Billing Coordinator

Public Health Nursing Consultant 1

Clinical Research Coordinator III

Report Coordinator - Flow Cytology

Biorepository Coordinator I PMI

Discharge Transport EMT

Admissions Coordinator

Intake Coordinator I

I want to receive the latest job alert for clinical data coordinator in nashville, tn

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