Top 28 Clinical research coordinator Jobs in Rock Hill Sc

Clinical Research Coordinator
Charlotte Gastroenterology & Hepatology —Charlotte, NC
- Full-time
- CPR Certification
- Nursing
- Patient monitoring
- Profit sharing
- Paid holidays
Quick Apply
Clinical Coordinator-Nursing
Southeastern College —Charlotte, NC
- Weekends as needed
- Nursing
- RN License
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
LPN Clinical Patient Services Coordinator
Amedisys —Chester, SC
- $22 - $28 an hour
- Full-time
- RN License
- Mid-level
- Administrative experience
Clinical Research Coordinator
DelRicht Research —Pineville, NC
- Full-time
- Blood sampling
- Urgent Care
- Clinic experience
- Profit sharing
- Disability insurance
6d
Clinical Research Coordinator I
Ora —Charlotte, NC
- Weekends as needed
- Vital signs
- Clinic experience
- Clinic
- Dental insurance
Quick Apply
Clinical Research Coordinator
Flourish Research —Charlotte, NC
- $28 - $34 a year
- Full-time
- Vital signs
- HIPAA
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
6d
Clinical Research Coordinator (Charlotte, NC)
SiteBridge Research, Inc. —Charlotte, NC
- $30 - $36 an hour
- Part-time
- Spanish
- Mid-level
- 3 years
Quick Apply
Clinical Coordinator - CMA, LPN
Your Health Organization —Rock Hill, SC
- 8 hour shift
- Mid-level
- Communication skills
- Health savings account
- 401(k)
Quick Apply
LPN Clinical Patient Services Coordinator
Amedisys, Inc. —Chester, SC
- $22 - $28 an hour
- Full-time
- RN License
- Mid-level
- Administrative experience
Registered Nurse Program Coordinator - Pediatric Clinical Research
Atrium Health —Charlotte, NC
- $38.20 - $57.30 an hour
- Full-time
- Nursing
- RN License
- Ability to walk for extended periods
- Paid parental leave
- Disability insurance
Clinical Operations Coordinator
Proactive MD —Charlotte, NC
- Full-time
- Nursing
- Microsoft Outlook
- Up to 50% travel
Quick Apply
10d
Clinical Research Nurse - AH Levine Children's Vaccine Trials - FT Day
Atrium Health —Charlotte, NC
- $38.20 - $57.30 an hour
- Full-time
- Spanish
- Nursing
- RN License
- Paid parental leave
- Disability insurance
Clinical Site Coordinator
CaroMont Health —Gastonia, NC
- Full-time
- RN License
- Customer service
- Mid-level
Clinical Services Coordinator (RN) - Community Based Palliative Care FT Days
Atrium Health —Charlotte, NC
- $38.20 - $57.30 an hour
- Full-time
- Nursing
- RN License
- BLS Certification
- Paid parental leave
- Disability insurance
10d
Shift Manager/Clinical Patient Placement Coordinator
CaroMont Health —Gastonia, NC
- PRN
- Nursing
- RN License
- PALS Certification
Oncology Research Specialist Registered Nurse - Atrium Health Levine Cancer Institute Clinical Trials
Atrium Health —Charlotte, NC
- $38.20 - $57.30 an hour
- Full-time
- CPR Certification
- Nursing
- RN License
- Paid parental leave
- Disability insurance
3d
Registered Clinical Nurse Program Coordinator
Atrium Health —Charlotte, NC
- $41.10 - $61.65 an hour
- Part-time
- Nursing
- RN License
- Hospital
- Paid parental leave
- Disability insurance
4d
Clinical Pharmacist - Pharmacy Operations Coordinator (Presbyterian Medical Center)
Novant Health —Charlotte, NC
- Monday to Friday
- Hospital
- Mid-level
- Bachelor's degree
9d
Clinical Coordinator - Infusion Center - Registered Nurse - Matthews
Novant Health —Matthews, NC
- Nursing
- RN License
- Bachelor of Science
Clinical Donation Coordinator I - PeeDee Region
WE ARE SHARING HOPE SC —United States
- On call
- Mid-level
- Operating room
- 2 years

I want to receive the latest job alert for clinical research coordinator in rock hill sc

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical research coordinator jobs near rock hill sc

Registered Nurse Oncology jobs in Charlotte, NC

Clinical Research Coordinator jobs in Charlotte, NC

Patient Coordinator jobs in Gastonia, NC

Clinical Pharmacist jobs in Charlotte, NC

Registered Nurse Pediatrics jobs in Charlotte, NC

Research Nurse jobs in Charlotte, NC

Nurse Coordinator jobs in Charlotte, NC

Clinic Operations Manager jobs in Charlotte, NC

Clinical Nurse jobs in Charlotte, NC

Site Coordinator jobs in Plaquemine, LA

Site Coordinator jobs in Washington, DC

Site Coordinator jobs in San Antonio, TX

Preschool Site Supervisor jobs in California

Site Coordinator jobs in Chicago, IL

Site Safety jobs in New York, NY

Live On Site Caretaker jobs in Minnesota

Outpatient Clinic Nurse jobs in Miami, FL

Remote Clinical Documentation Specialist jobs in Wisconsin

Clinical Research Associate jobs in San Diego, CA

Clinical Nurse Manager jobs in Rock Hill, SC

Clinical Research Coordinator

Charlotte Gastroenterology & Hepatology -
Charlotte, NC

Quick Apply

Job Details

Full-time

Benefits

Profit sharing
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

BLS Certification
Medical scheduling
Medical administrative support
Quality control
Data collection
FDA regulations

Full Job Description

Charlotte Gastro is seeking an experienced Clinical Research Coordinator to manage clinical research studies in a fast-paced healthcare environment. This role independently coordinates clinical trials while ensuring compliance with Good Clinical Practice (GCP) regulations, organizational policies, and study protocols. The ideal candidate will possess strong research coordination experience, and excellent organizational and communication skills.

ESSENTIAL FUNCTIONS:

1. Administrative:

a. Attend and participate in Clinical Research Meetings and other regional or national research meetings.

b. Review research journals and pertinent publications.

c. Developing/maintaining standard operating procedures, QA/QC standards to ensure compliance with industry standards.

2. Site Preparation:

a. Schedule and coordinate pre-study site visit.

b. Preparation of regulatory documents for Sponsor

c. Preparation and submission of IRB documents

d. Prepare space for study-related equipment and supplies.

e. Present clinical trial timelines to study teams

f. Educate staff regarding scientific aspects of the study.

g. Train/educate ancillary staff regarding clinical trials.

h. Coordinate study initiation.

3. Study Conduct:

a. Perform subject interviews and assessments at study visits as required by protocol.

b. Monitor study team compliance with required study procedures and GCP/ICH standards.

c. Assess and ensure subject safety throughout participation in trial.

d. Maintain patient and study confidentiality at all times.

e. Develop appropriate patient education tools to ensure patient understanding and compliance.

4. Recruitment

a. Screen medical records, interview and schedule visits for potential subjects.

b. Prepare/place advertisements and prepare screening sheets/logs as needed.

c. Utilize computer-generated diagnosis (ICD-9).

d. Monitor enrollment goals and modify recruitment strategies as needed.

e. Explain concept of clinical research and provide patient teaching on disease entity.

5. Screening:

a. Review and obtain medical histories, demographics, etc.

b. Obtain other pertinent medical records as required.

c. Provide adequate documentation in medical records of screening attempts and conversations.

6. Scheduling of Patients:

a. Coordinate subject visits as per protocol and with other support services

b. Call or send reminders of scheduled visits as needed.

7. Informed Consent:

a. Explain study to subjects

b. Obtain all required signatures.

c. Provide subject with copy of signed informed consent.

d. Document obtaining informed consent in medical records.

8. Case Report Forms:

a. Review inclusion/exclusion criteria, document concomitant medications, and review medical history.

b. Enter data for specific visit on CRF or with Remote Data Entry (if applicable).

c. Audit for accuracy and correct CRF’s.

d. Transmit data by fax, express mail, etc.

e. Complete and return Sponsor queries promptly.

9. Source Documentation:

a. Develop and/or maintain study specific progress notes for documentation of study visits.

b. Incorporate applicable historical documents

c. Maintain status reports and subject logs.

d. Document written and verbal communication with study contacts

e. Schedule and prepare for monitoring visits or audits.

f. Record and document protocol deviations.

g. Maintain communications with the IRB with regard to initial submission, annual/quarterly updates, adverse events, safety reports, protocol amendments, informed consent, modifications, changes in personnel or site locations, etc.)

10. Test Article Accountability:

a. Store test article supplies in accordance to FDA and Sponsor guidelines.

b. Receive, inventory, and maintain test article at site.

c. Dispense and retrieve test articles according to protocol.

d. Order supplemental test articles and supplies as needed.

e. Return used and unused test articles to Sponsor or designee.

f. Maintain randomization and emergency codes of test article.

g. Document on accountability log and subject medical records.

h. Manage DEA controlled drugs, if applicable.

11. Laboratory Issues:

a. Ensure proper collection, processing, and shipment of specimens (centrifuge, preparation of slides, freezing, refrigeration, etc.)

b. Utilize or develop procedure and collection forms for pharmacokinetic collection and storage.

c. Communicate with laboratory, physician, and Sponsor regarding laboratory findings.

d. Maintain OSHA standards.

e. Maintain supply inventory.

f. Maintain equipment (e.g., calibration and preventative maintenance).

g. Recognize common laboratory values and alerts.

h. Assure current laboratory certification and normal ranges are provided.

i. Complete and maintain Hazardous Materials Transport Training.

12. Adverse Events:

a. Apply pharmacological Knowledge and utilize reference manuals to assist the Investigator in determining idiosyncrasies, casualty, expected or unexpected results.

b. Observe, query, and document medical events.

c. Present Investigator with relevant information for determination of seriousness, casualty, and intervention.

d. Act on Investigator recommendation for adverse event.

e. Maintain follow-up to determine resolution of adverse event.

f. Report serious adverse events to Sponsor and IRB.

g. Assist Investigator in classifying adverse events

h. Record adverse events and relevant information in source document, CRF, and Sponsor specific forms).

13. Close-out:

a. Schedule and prepare for close-out visit.

b. Return or dispose of unused supplies per Sponsor requirements.

c. Reconcile test article accountability.

d. Audit documents and pertinent files and prepare for storage.

e. Maintain documents as required by FDA/Sponsor guidelines.

f. Prepare study summary for Sponsor.

g. Provide method of document retrieval from storage.

h. Document drop-outs (e.g., causes, contact efforts).

i. Prepare for and respond to Sponsor and FDA audits.

EDUCATION: RN graduate from accredited school of nursing, LPN graduate from accredited school of nursing, Medical Asst/Medical Technologist, or Certified Clinical Research Coordinator.

EXPERIENCE: Musthave experience with clinical trials.

CERTIFICATES AND LICENSES: Current certifications by appropriate licensing board as well as CPR/BLS certified.

BENEFITS:

1. Paid time off (PTO)

2. Paid holidays

3. Employee health, dental, vision insurance, life & disability insurance

5. 401K and Profit-Sharing Plan

Charlotte Gastro is proud to be an Equal Opportunity Employer. We do not discriminate based on race, color, gender, disability, protected veteran, military status, religion, age, creed, national origin, gender, identity, sexual orientation, marital status, genetic information, or any other basis prohibited by local, state, or federal law.

Work Location: In person

Quick Apply

Refine Your Search

clinical research coordinator jobs in rock hill sc

Clinical Research Coordinator

Clinical Coordinator-Nursing

LPN Clinical Patient Services Coordinator

Clinical Research Coordinator

Clinical Research Coordinator I

Clinical Research Coordinator

Clinical Research Coordinator (Charlotte, NC)

Clinical Coordinator - CMA, LPN

LPN Clinical Patient Services Coordinator

Registered Nurse Program Coordinator - Pediatric Clinical Research

Clinical Operations Coordinator

Clinical Research Nurse - AH Levine Children's Vaccine Trials - FT Day

Clinical Site Coordinator

Clinical Services Coordinator (RN) - Community Based Palliative Care FT Days

Shift Manager/Clinical Patient Placement Coordinator

Oncology Research Specialist Registered Nurse - Atrium Health Levine Cancer Institute Clinical Trials

Registered Clinical Nurse Program Coordinator

Clinical Pharmacist - Pharmacy Operations Coordinator (Presbyterian Medical Center)

Clinical Coordinator - Infusion Center - Registered Nurse - Matthews

Clinical Donation Coordinator I - PeeDee Region

I want to receive the latest job alert for clinical research coordinator in rock hill sc

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected