Top 45 Clinical research associate Jobs in South Carolina

Clinical Research Assistant / Medical Assistant
Alcanza Clinical Research —Charleston, SC
- Full-time
- Spanish
- Vital signs
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
Clinical Research Coordinator
DelRicht Research —Mount Pleasant, SC
- Full-time
- Blood sampling
- Urgent Care
- Clinic experience
- Profit sharing
- Disability insurance
Clinical - Clinical Research Coordinator
Tribe Clinical Research —Greenville, SC
- Full-time
- Computer literacy
- Writing skills
- Mid-level
Quick Apply
Manager, Clinical Trial Management
Precision Medicine Group —North, SC
- $133,900 - $200,900 a year
- Online Application
- Remote
- Microsoft Excel
- Microsoft Outlook
- 5 years
Clinical Research Assistant
Headlands Research —Myrtle Beach, SC
- Full-time
- Vital signs
- Clinic
- Medical terminology
- Health savings account
- Paid holidays
4d
Clinical Research Coordinator I (Temp Position Tentatively July 20, 2026-July 20, 2027)
Shriners Hospitals for Children —Greenville, SC
- $21.74 - $32.62 an hour
- Temporary
- 18 years or older
- Spanish
- English
Quick Apply
Clinical Research Coordinator
Solaris Health Holdings LLC —North Charleston, SC
- Full-time
- Nursing
- BLS Certification
- HIPAA
Quick Apply
Clinical Research Assistant
Velocity Clinical Research, Inc. —Union, SC
- Full-time
- Vital signs
- English
- High school diploma or GED
- Paid holidays
- Health insurance
Quick Apply
9d
Stroke Research Coordinator II, Administrative Research, FT Days
Prisma Health —Greenville, SC
- Full-time
- Hospital
- Mid-level
- Bachelor's degree
Research Nurse
University of South Carolina —South Carolina
- $39 an hour
- Part-time
- Nursing
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Flexible spending account
Research Program Coordinator I
University of South Carolina —South Carolina
- $25 an hour
- Weekends as needed
- Microsoft Excel
- Microsoft Outlook
- In-person
- Health insurance
- Flexible spending account
CRA 2/Senior CRA 1
IQVIA —Columbia, SC
- $90,200 - $175,100 a year
- Full-time
- Bachelor's degree
- Experience equivalent to degree accepted
- 1 year
Healthcare Data Entry Coordinator - Onsite in Charleston, SC
Alcanza Clinical Research —Charleston, SC
- Full-time
- HIPAA
- High school diploma or GED
- Neurology
- Health savings account
- Disability insurance
Quick Apply
4d
Medical Assistant
DelRicht Research —Mount Pleasant, SC
- Full-time
- Blood sampling
- Urgent Care
- Clinic experience
- Profit sharing
- Disability insurance
Coord-Clinical Research
Spartanburg Regional Healthcare System —Spartanburg, SC
- Full-time
- Nursing
- RN License
- Hospital
Quick Apply
Clinical Research Coordinator (Walhalla, SC)
SiteBridge Research, Inc. —Walhalla, SC
- $30 - $36 an hour
- Part-time
- Spanish
- English
- Mid-level
Quick Apply
Clinical Scientist - Oncology
サイネオス・ヘルス —South Carolina
- Remote
- Mid-level
- Employee stock purchase plan
- Health insurance
CLINICAL RESEARCH COORDINATOR
StrideCare —Charleston, SC
- Full-time
- Spanish
- LVN
- HIPAA
Quick Apply
Clinical Trial Manager - Full Service
サイネオス・ヘルス —South Carolina
- Remote
- Computer literacy
- Bachelor's degree
- Travel
- Employee stock purchase plan
- Health insurance
Research Coordinator II - FT, Days
Prisma Health —Columbia, SC
- Full-time
- Hospital
- Mid-level
- Bachelor's degree
19h

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Clinical Research Assistant / Medical Assistant

Alcanza Clinical Research -
Charleston, SC

Quick Apply

Job Details

Full-time

Benefits

Health savings account
Disability insurance
Health insurance
Dental insurance
401(k)
Vision insurance
401(k) matching
Life insurance

Qualifications

Computer operation
Electronic health records (EHR) management
HIPAA
Administrative experience
High school diploma or GED
Health information regulatory compliance
Typing
Clinical confidentiality policies

Full Job Description

Description

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.

The Research Assistant (RA) provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. The RA performs clinical, lab, and administrative tasks as needed for the successful operation of the clinical research site.

Key Responsibilities

Essential Job Duties: In collaboration with other members of the clinical research site team, assists with the execution of assigned studies, and support functions as needed. Responsibilities may include but are not limited to:

Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol:
- Assists with the basic screening of patients for study enrollment;
- Assists with patient follow-up visits;
- Documents in source clinic charts;
- Enters data in EDC and answers queries;
- Obtains vital signs and ECGs;
- May perform blood draws;
- Perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
- Request and track medical record requests;
- Enters data in EDC and answers queries;
- Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and
- Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed;
Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
Assists the CRC and/or Manager with study recruitment, patient enrollment, and tracking as needed;
Maintains strict confidentiality of patients, employees, customers and company information at all times and adheres to HIPAA Guidelines; and
Perform all other duties as requested or assigned.

Skills, Knowledge and Expertise

Minimum Qualifications: A High School diploma and 1 year of administrative / clinical experience is required. 1 year or more years of clinical research or clinical experience is preferred. Bi-lingual (English / Spanish) proficiency is a plus.

Required Skills:

Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm).
Must possess strong organizational skills and attention to detail.
Well-developed written and verbal communication skills.
Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
Must be professional, respectful of others, self-motivated, and have a strong work ethic.
Must possess a high degree of integrity and dependability.
Ability to work under minimal supervision, identify problems and implement solutions.
Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits

Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

About Alcanza Clinical Research

Alcanza Clinical Research (“Alcanza”) is a national, collaborative network of clinical research sites, founded on the mission to accelerate the development of new therapies by reducing barriers to clinical research participation for all.

We conduct research on dozens of conditions in several therapeutic areas including psychiatry, neurology, dermatology, and infectious disease. Our work is important to the patients who participate, the scientists who develop these new therapies, and the entire medical community. Because all approved medications require clinical trials, the impact of your work is exponential, reaching many thousands of future patients and improving their quality of life.

Alcanza is a culturally competent organization. We treat each other with dignity, creating an environment where all individuals feel welcome, heard, and respected for their unique perspectives and aspirations. We put considerable effort into finding exceptional employees who mirror the values most important to us: Inclusive, Impactful, Compassionate, and Determined.

Alcanza Clinical Research is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, marital status, veteran status, disability, sexual orientation, gender identity or expression, genetic information, or any other category protected by law. We recognize that diversity and inclusion is a driving force in the success of our company.

Quick Apply

Refine Your Search

clinical research associate jobs in south carolina

Clinical Research Assistant / Medical Assistant

Clinical Research Coordinator

Clinical - Clinical Research Coordinator

Manager, Clinical Trial Management

Clinical Research Assistant

Clinical Research Coordinator I (Temp Position Tentatively July 20, 2026-July 20, 2027)

Clinical Research Coordinator

Clinical Research Assistant

Stroke Research Coordinator II, Administrative Research, FT Days

Research Nurse

Research Program Coordinator I

CRA 2/Senior CRA 1

Healthcare Data Entry Coordinator - Onsite in Charleston, SC

Medical Assistant

Coord-Clinical Research

Clinical Research Coordinator (Walhalla, SC)

Clinical Scientist - Oncology

CLINICAL RESEARCH COORDINATOR

Clinical Trial Manager - Full Service

Research Coordinator II - FT, Days

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