Top 29 Clinical research associate Jobs in Charleston Sc

Clinical Research Coordinator, Registered Nurse
Advanced Urology Institute LLC —North Charleston, SC
- Full-time
- Nursing
- Blood sampling
- RN License
Quick Apply
Clinical Research Coordinator
DelRicht Research —Mount Pleasant, SC
- Full-time
- Blood sampling
- Urgent Care
- Clinic experience
- Profit sharing
- Disability insurance
7d
Clinical Research Assistant / Medical Assistant
Alcanza Clinical Research —Charleston, SC
- Full-time
- Spanish
- Vital signs
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
10d
Clinical Research Coordinator
Solaris Health Holdings LLC —North Charleston, SC
- Full-time
- Nursing
- BLS Certification
- HIPAA
Quick Apply
Clinical Research Coordinator
Alcanza Clinical Research —Charleston, SC
- Full-time
- Spanish
- LVN
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
Per Diem Clinical Research Nurse - Home Visits
Science 37 —Charleston, SC
- $50 - $55 an hour
- Nights as needed
- Nursing
- RN License
- BLS Certification
Medical Assistant
DelRicht Research —Mount Pleasant, SC
- Full-time
- Blood sampling
- Urgent Care
- Clinic experience
- Profit sharing
- Disability insurance
7d
UNIV - Clinical Research Assistant - Department of Medicine: Division of Pulmonary
MUSC —Charleston, SC
- $37,200 - $59,500 a year
- Full-time
- Mid-level
- 3 years
- High school diploma or GED
CLINICAL RESEARCH COORDINATOR
StrideCare —Charleston, SC
- Full-time
- Spanish
- LVN
- HIPAA
Quick Apply
UNIV - Research Program Coordinator I - Novice - Department of Ophthalmology
MUSC —Charleston, SC
- $45,300 - $77,000 a year
- Full-time
- Clinic
- Bachelor's degree
- 1 year
Clinical Trials Coordinator (1-2 years of experience)
Clinical Trials of South Carolina —Charleston, SC
- Full-time
- Mid-level
- Bachelor's degree
- Neurology
- Health insurance
- Dental insurance
Quick Apply
PRN Clinical Lab Assistant -MUSC Maybank Johns Island - MUSCP
MUSC —Mount Pleasant, SC
- Part-time
- Ability to climb stairs
- High school diploma or GED
- Ability to lift 50 pounds
12d
Senior Data Team Lead (Remote)
IQVIA —Charleston, SC
- $86,800 - $217,100 a year
- Full-time
- Remote
- 7 years
- Bachelor's degree
- Continuous improvement
- Health insurance
- Dental insurance
Paramedic - Weekday evenings (Between 7pm-7am) and weekend shifts needed - PRN
Alcanza Clinical Research —Charleston, SC
- Part-time
- Spanish
- BLS Certification
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
UNIV - Data Core Coordinator - Hollings Cancer Center
MUSC —Charleston, SC
- $52,100 - $88,600 a year
- Full-time
- OSHA
- Databases
- University
UNIV - Program Manager I – EP, Structural & Preventative Cardiology Clinical Trials - Department of Medicine: Division of Cardiology
MUSC —Charleston, SC
- $66,400 - $119,500 a year
- Weekends as needed
- 3 years
- University
- Bachelor's degree
UNIV - Regulatory Coordinator - Department of Medicine: Division of Pulmonary
MUSC —Charleston, SC
- $45,300 - $77,000 a year
- Full-time
- Mid-level
- Databases
- University
7d
UNIV - Research Program Assistant: Advanced - Department of Otolaryngology
MUSC —Charleston, SC
- $37,200 - $59,500 a year
- Full-time
- Adults
- High school diploma or GED
- Bachelor's degree
Program Coordinator RN - MUSCP
MUSC —Charleston, SC
- Weekends as needed
- Nursing
- RN License
- BLS Certification
UNIV - SISU Start-Up Manager & Protocol Writer - Hollings Cancer Center
MUSC —Charleston, SC
- $66,400 - $119,500 a year
- Full-time
- 3 years
- Bachelor's degree
- Contracts
12d

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Clinical Research Coordinator, Registered Nurse

Advanced Urology Institute LLC -
North Charleston, SC

Quick Apply

Job Details

Full-time

Qualifications

RN License
BLS Certification

Full Job Description

Description:

GENERAL SUMMARY

Clinical Research Coordinator, RN’s are primarily responsible for study coordination and data management, with a central focus on managing subject recruitment and enrollment, consistency of study implementation, data management and integrity, and compliance with regulatory requirements and reporting.

Requirements:

ESSENTIAL JOB FUNCTION/COMPETENCIES

The responsibilities and duties described in this job description are intended to provide a general overview of the position. Duties may vary depending on the specific needs of the affiliate or location you are working at and/or state requirements. Responsibilities include but are not limited to:

Maintain site compliance for all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
Maintain working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s).
Complete all relevant Profound Research required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner.
Educates and directs protocol compliance with physicians and staff.
Assists in developing tools to meet requirements of new protocols.
Manages protocols with increased clinical complexities including translational investigator-initiated research as well as multi center trials.
Ensure good documentation practices are applied by all team members when collecting, maintaining, and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
Acts as a patient advocate by providing education to and responding to questions from patients about protocols.
Works with patients to ensure adherence with the protocol.
Collaborates with scheduling staff to assure that future appointments for the patients (follow up visits and diagnostic testing) are scheduled correctly and timely.
Collaborates with the physician to assure orders for treatment are written per protocol and delivered at the prescribed protocol intervals.
Performs other position related duties as assigned.
Employees shall adhere to high standards of ethical conduct and will comply with and assist in complying with all applicable laws and regulations. This will include and not be limited to following the Solaris Health Code of Conduct and all Solaris Health and Affiliated Practice policies and procedures; maintaining the confidentiality of patients' protected health information in compliance with the Health Insurance Portability and Accountability Act (HIPAA); immediately reporting any suspected concerns and/or violations to a supervisor and/or the Compliance Department; and the timely completion the Annual Compliance Training.

CERTIFICATIONS, LICENSURES OR REGISTRY REQUIREMENTS

BLS certification required, ACLS preferred.
RN licensure and certifications as required by State.
Clinical research certification from SoCRA (Society of Clinical Research Associates) or ACRP (Association of Clinical Research Professionals) preferred.

KNOWLEDGE | SKILLS | ABILITIES

Ability to Start IVs and Administer IV medications
Ability to draw blood
Understanding of all aspects of biomedical research protocols, ensuring applicable regulations, and guidelines.
Maintains patient confidentially.
Excellent verbal and written communication skills.
Skill in using computer programs and applications.
Maintains current knowledge and awareness of organizational and regulatory standards, policies and procedures.
Excellent organizational skills and attention to detail.
Ability to build relationships with patients and display empathy and compassion to patients
Skill in using computer programs and applications including Microsoft Office.
Complies with HIPAA regulations for patient confidentiality.
Complies with all health and safety policies of the organization.

EDUCATION REQUIREMENTS

Must be a Registered Nurse (RN) with a current and valid license. Associate’s or Bachelor’s degree in Nursing (ASN or BSN) required.

EXPERIENCE REQUIREMENTS

2 or more years Nursing experience in ICU, ER, oncology or clinical trial experience, preferred.

REQUIRED TRAVEL

May require travel to other site locations in practice.
May require travel to Investigator and other meetings.

PHYSICAL DEMANDS

Carrying Weight Frequency

1-25 lbs. Frequent from 34% to 66%

26-50 lbs. Occasionally from 2% to 33%

Pushing/Pulling Frequency

1-25 lbs. Seldom, up to 2%

100 + lbs. Seldom, up to 2%

Lifting - Height, Weight Frequency

Floor to Chest, 1 -25 lbs. Occasional: from 2% to 33%

Floor to Chest, 26-50 lbs. Seldom: up to 2%

Floor to Waist, 1-25 lbs. Occasional: from 2% to 33%

Floor to Waist, 26-50 lbs. Seldom: up to 2%

Version 6.2.25

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Refine Your Search

clinical research associate jobs in charleston sc

Clinical Research Coordinator, Registered Nurse

Clinical Research Coordinator

Clinical Research Assistant / Medical Assistant

Clinical Research Coordinator

Clinical Research Coordinator

Per Diem Clinical Research Nurse - Home Visits

Medical Assistant

UNIV - Clinical Research Assistant - Department of Medicine: Division of Pulmonary

CLINICAL RESEARCH COORDINATOR

UNIV - Research Program Coordinator I - Novice - Department of Ophthalmology

Clinical Trials Coordinator (1-2 years of experience)

PRN Clinical Lab Assistant -MUSC Maybank Johns Island - MUSCP

Senior Data Team Lead (Remote)

Paramedic - Weekday evenings (Between 7pm-7am) and weekend shifts needed - PRN

UNIV - Data Core Coordinator - Hollings Cancer Center

UNIV - Program Manager I – EP, Structural & Preventative Cardiology Clinical Trials - Department of Medicine: Division of Cardiology

UNIV - Regulatory Coordinator - Department of Medicine: Division of Pulmonary

UNIV - Research Program Assistant: Advanced - Department of Otolaryngology

Program Coordinator RN - MUSCP

UNIV - SISU Start-Up Manager & Protocol Writer - Hollings Cancer Center

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