Top 11 Clinical research associate Jobs in North Charleston, Sc

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
13d
EMT/Paramedic - Weekday evenings (Between 7pm-7am) and weekend shifts needed - PRN
Alcanza Clinical Research —Charleston, SC
- Part-time
- HIPAA
- Mid-level
- ACLS Certification
- 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 Research Assistant / Medical Assistant
Alcanza Clinical Research —North Charleston, SC
- Full-time
- Spanish
- Vital signs
- HIPAA
- Health savings account
- Disability insurance
Quick Apply
9d
Medical Assistant
DelRicht Research —Mount Pleasant, SC
- Full-time
- Blood sampling
- Urgent Care
- Clinic experience
- Profit sharing
- Disability insurance
CLINICAL RESEARCH COORDINATOR
StrideCare —Charleston, SC
- Full-time
- Spanish
- LVN
- HIPAA
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

Discover related jobs

Based on your search for clinical research associate jobs.

Healthcare Data Entry Coordinator - Onsite in Charleston, SC
Alcanza Clinical Research —Charleston, SC
In collaboration with other members of the clinical research site teamwork to ensure the entry of clinical visit data in EDC and other clinical data software/…
Quick Apply
13d
Clinical Research Coordinator
DelRicht Research —Mount Pleasant, SC
If the answer is yes, then DelRicht Research might be the right opportunity for you! RN, LPN, MA, scribe, urgent care, EDC entry, or other clinical background.

Show more related jobs

Explore jobs in cities nearby

Check out jobs in cities near your current location, Columbus

Research Assistant
OhioHealth —Columbus, OH
Manages complex administrative tasks in support of research administration and clinical trials, including but not limited to screening patients, entering/…
Clinical Research Coordinator I (CRC I)
Centricity Research —Columbus, OH
Bachelor’s degree in a health, science, or research-related field, or an equivalent combination of education and relevant experience.
$50,000 - $52,000 a year
Quick Apply
11d

Show more jobs in cities nearby

I want to receive the latest job alert for clinical research associate in north charleston, 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 associate jobs near north charleston, sc

Clinical Research Coordinator jobs in Charleston, SC

Healthcare Coordinator jobs in Charleston, SC

Medical Assistant jobs in Mount Pleasant, SC

Emergency Medical Technician jobs in Charleston, SC

Neuroscience Research jobs in Connecticut

Research Nurse jobs in Oklahoma City, OK

Research Nurse jobs in Iowa City, IA

Research Scientist jobs in Minneapolis, MN

Dermatology Nurse jobs in Philadelphia, PA

Research Nurse jobs in New Jersey

Research Nurse jobs in Utah

Remote Clinical Trial Assistant jobs in New Jersey

Clinical Research Coordinator jobs in Dallas Fort Worth, TX

Research Nurse jobs in Sacramento, CA

Clinical Research Coordinator jobs in Boise, ID

Clinical Research Coordinator jobs in Arizona

Clinical Research Coordinator jobs in Stony Brook, NY

Clinical Informatics jobs in Washington, DC

Healthcare Coordinator jobs in Cranston, RI

Healthcare Coordinator jobs in Alexandria, LA

Healthcare Data Entry Coordinator - Onsite in Charleston, SC

Alcanza Clinical Research -
Charleston, SC

Quick Apply

Job Details

Full-time
13 days ago

Benefits

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

Qualifications

HIPAA
Desktop applications
Health information regulatory compliance
Typing
Productivity software
Clinical confidentiality policies
Quality data entry

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 Data Entry Coordinator works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.

Key Responsibilities

Essential Job Duties:

In collaboration with other members of the clinical research site teamwork to ensure the entry of clinical visit data in EDC and other clinical data software/systems. Responsibilities may include but are not limited to:

Managing data entry into computer systems for clinical trials, including entering patient data into eDC and other software
Reviewing patient charts and other medical records to ensure data is entered in a timely manner in accordance with eCRF guidelines and protocol requirements
Reporting any irregularities or problems with a study to the appropriate parties
Supporting other clinical research-related activities
Ensuring compliance with SOPs, regulations, ICF documentation, and GCP/GDP guidelines
Maintaining confidentiality of patients, customers, and company information, and performing other related activities as assigned.

Skills, Knowledge and Expertise

Minimum Qualifications: High School diploma or equivalent and a minimum of 1 year of clinical data entry experience, or an equivalent combination of education and experience.

Required Skills:

Proficiency with computer applications such as Microsoft applications, email, and web applications, and the ability to type proficiently (40+ wpm);
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 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 north charleston, sc

Healthcare Data Entry Coordinator - Onsite in Charleston, SC

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

Clinical Research Coordinator

Clinical Research Assistant / Medical Assistant

Medical Assistant

CLINICAL RESEARCH COORDINATOR

Per Diem Clinical Research Nurse - Home Visits

Discover related jobs

Explore jobs in cities nearby

I want to receive the latest job alert for clinical research associate in north charleston, sc

Explore jobs in more locations

Description

Key Responsibilities

Skills, Knowledge and Expertise

Benefits

About Alcanza Clinical Research

Job Seeker Tools

Employer Tools

Browse

Stay Connected