Top 226 Clinical data coordinator Jobs in Atlanta Ga

Clinical Research Coordinator
Rare Disease Research, LLC —Brookhaven, GA
- $26 - $28 an hour
- 8 hour shift
- CPR Certification
- Blood sampling
- Patient monitoring
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Data Coordinator I- Winship Cancer Institute
Emory University —Atlanta, GA
- Full-time
- Customer service
- HIPAA
- Administrative experience
Clinical Research Coordinator I (ETS) | Temporary
Emory Healthcare —Atlanta, GA
- $21.01 - $28.22 an hour
- Part-time
- Customer service
- Administrative experience
- High school diploma or GED
5d
Clinical Research Coordinator - Marietta, GA
IQVIA —Marietta, GA
- $35 - $42 an hour
- Part-time
- Vital signs
- Office
- Bachelor's degree
Remote Clinical Quality Improvement Coordinator
Guidehealth —Atlanta, GA
- $28 - $30 an hour
- Full-time
- Remote
- Microsoft Excel
- Mid-level
- LPN
- Paid parental leave
- Disability insurance
Clinical Research Data Coordinator II - Winship Cancer Institute
Emory University —Atlanta, GA
- Full-time
- HIPAA
- Mid-level
- High school diploma or GED
3d
Clinical Research Coordinator I - School of Medicine Neurology
Emory University —Atlanta, GA
- Full-time
- Hybrid work
- Customer service
- Mid-level
- Administrative experience
- Work from home
Clinical Research & Data Coordinator
Morehouse School Of Medicine —Atlanta, GA
- HIPAA
- Mid-level
- University
Clinical Research Coordinator I- School of Medicine, Cardiology
Emory University —Atlanta, GA
- Full-time
- Customer service
- Mid-level
- Administrative experience
Clinical Research Coordinator I- School of Medicine, Nephrology
Emory University —Atlanta, GA
- Full-time
- Customer service
- Mid-level
- Administrative experience
Clinical Research Coordinator I (ETS) | Temporary
Emory University —Atlanta, GA
- Part-time
- Customer service
- Mid-level
- Administrative experience
5d
Coding & Documentation Coordinator
Emory Healthcare —Atlanta, GA
- $37.44 - $45.62 an hour
- Full-time
- Mid-level
- Wellness program
- Health insurance
Clinical Research Coordinator I-School of Medicine, Georgia CTSA
Emory University —Atlanta, GA
- Full-time
- Customer service
- Mid-level
- Administrative experience
Clinical Research Coordinator II - School of Medicine Neurology
Emory University —Atlanta, GA
- Full-time
- Medicine
- Mid-level
- Databases
Clinical Research Coordinator III- SOM, Infectious Diseases (Hope Clinic)
Emory University —Decatur, GA
- Full-time
- Remote
- Management
- High school diploma or GED
- University
Clinical Research Coordinator I- School of Medicine, Kaplan Speech EMA
Emory University —Atlanta, GA
- Part-time
- Hybrid work
- Medicine
- Customer service
- Mid-level
- Work from home
Clinical Research Coordinator III
Denali Health —Atlanta, GA
- Nursing
- Mid-level
- 3 years
Quick Apply
Program Coordinator-Georgia Clinical & Translational Science Alliance
Emory University —Atlanta, GA
- Full-time
- Hybrid work
- Microsoft Excel
- Mid-level
- Bachelor's degree
- Work from home
6d
Clinical Research Coordinator I - The School of Nursing - Alzheimer's Disease Prevention
Emory University —Atlanta, GA
- Full-time
- Nursing
- Customer service
- Mid-level
Clinical Research Coordinator IV - School of Medicine, Emergency Medicine
Emory University —Atlanta, GA
- Full-time
- Hybrid work
- Management
- High school diploma or GED
- University
- Work from home

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Clinical Research Coordinator

Rare Disease Research, LLC
Brookhaven, GA

Quick Apply

Job Details

Full-time
$26 - $28 an hour

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching

Qualifications

Clinical research
BLS Certification
Clinical trials

Full Job Description

About Rare Disease Research:

As an independent clinical research site, we are 100% dedicated to conducting clinical research, accelerating the development of safe and effective treatments and providing rare disease patients with access to innovative investigational therapies. We are a passionate, caring, multi-disciplinary team conducting clinical research with expertise and compassion, and always to the highest ethical standards.

About This Opportunity:

We are looking for a clinical research coordinator who has at least 1 year experience with the conduction of clinical research to join our wonderful team of motivated research professionals. Ideally, the right candidate has prior clinical research experience conducting investigational clinical trials and is already familiar with clinical research workflows, regulatory requirements, and data collection and documentation practices.

* Important Note: Applicants for employment in the United States must have work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States and with Rare Disease Research.

Responsibilities:

Assists Principal Investigator (PI) in protection of the rights and welfare of all human research participants involved in research in accordance with federal regulations and university and sponsoring agency policies and procedures.
Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.
Collaborates with PI and institution to respond to any audit findings and implement approved recommendations.
Reviews and develops a familiarity with the protocol, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.
Collects documents needed to initiate the study and submit to the sponsor (e.g., Form FDA 1572, CVs, etc.).
Works with the PI to develop and implement recruitment strategies in accordance with HRPO (IRB) requirements and approvals.
Conducts or participates in the informed consent process including interactions with the HRPO (IRB) and discussions with research participants, including answering any questions related to the study. Obtains appropriate signatures and dates on forms in appropriate places. Assures that amended consent forms are appropriately implemented and signed.
Screens subjects for eligibility using protocol specific inclusion and exclusion criteria, documenting each potential participant’s eligibility or exclusion.
Performs safety and efficacy assessments per study protocol.
Collect or coordinate collection of clinical procedures such as vital signs, ECGs, blood draws, IP infusions.
Responsible for timely data entry and query resolutions.
Reports study findings, such as serious adverse events (SAEs) or protocol deviations (PDs) to the applicable department, such as the sponsor or IRB.
Manages participant chart binders and coordinates accurate completion of source with various delegated staff.
Follows participants from the start to end of study participation and escalates safety concerns to appropriate individuals, such as the PI or Medical Monitor.
Prepare study data for interim monitoring visits and meet with study monitor to follow-up on resolving queries/issues.
Communicate with sponsors, CROs, vendors, or other representatives promptly and professionally.
Completes study documentation and maintains study files in accordance with sponsor requirements and University policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.
Updates source documents per study protocol amendment.
Coordinate operations with other departments to facilitate completion of procedures during participant visits, includes communications with nurse practitioners, medical assistants, pharmacy, regulatory, and/or physical therapy.
Retains all study records in accordance with sponsor requirements.
Works with the PI and study-specific RAs to manage the day to day activities of the study including problem solving, communication, and protocol management.
Ability to exercise independent judgment and discretion

The above statements are intended only to describe the general nature of the job, and should not be construed as an all-inclusive list of position responsibilities.

Requirements:

Secondary degree in social science, health science or related field
Alternative educational backgrounds may be accepted (i.e., LPN, Medical Assistant, etc) in combination with previous CRC experience
Must have GCP, IATA, ALCOAC training
BLS/CPR training upon hire date
2 years of experience in the clinical research field
At least 1 year previous experience as a CRC
Fully vaccinated against COVID-19 and willing to receive annual flu vaccination

Job Type: Full-time

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Vision insurance

Schedule:

8 hour shift
Day shift
Monday to Friday

Ability to commute/relocate:

Atlanta, GA 30329: Reliably commute or planning to relocate before starting work (Required)

Work Location: One location, on site and in person

Rare Disease Research is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran status, or any other characteristic protected by federal, state or local laws.

Notice To Third-Party Agencies:

Rare Disease Research does not accept unsolicited resumes from recruiters or agencies. Any staffing/employment agency, person or entity that submits an unsolicited resume to this site does so with the understanding that the applicant's resume will become the property of Rare Disease Research will have the right to hire that applicant at its discretion and without any fee owed to the submitting staffing/employment agency, person, or entity.

Job Type: Full-time

Pay: $26.00 - $28.00 per hour

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Paid time off
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

clinical data coordinator jobs in atlanta ga

Clinical Research Coordinator

Clinical Research Data Coordinator I- Winship Cancer Institute

Clinical Research Coordinator I (ETS) | Temporary

Clinical Research Coordinator - Marietta, GA

Remote Clinical Quality Improvement Coordinator

Clinical Research Data Coordinator II - Winship Cancer Institute

Clinical Research Coordinator I - School of Medicine Neurology

Clinical Research & Data Coordinator

Clinical Research Coordinator I- School of Medicine, Cardiology

Clinical Research Coordinator I- School of Medicine, Nephrology

Clinical Research Coordinator I (ETS) | Temporary

Coding & Documentation Coordinator

Clinical Research Coordinator I-School of Medicine, Georgia CTSA

Clinical Research Coordinator II - School of Medicine Neurology

Clinical Research Coordinator III- SOM, Infectious Diseases (Hope Clinic)

Clinical Research Coordinator I- School of Medicine, Kaplan Speech EMA

Clinical Research Coordinator III

Program Coordinator-Georgia Clinical & Translational Science Alliance

Clinical Research Coordinator I - The School of Nursing - Alzheimer's Disease Prevention

Clinical Research Coordinator IV - School of Medicine, Emergency Medicine

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