Top 9 Clinical data manager Jobs in Greenville Sc

Stroke Research Coordinator II, Administrative Research, FT Days
Prisma Health —Greenville, SC
- Full-time
- Hospital
- Mid-level
- Bachelor's degree
Operations - Site Lead
Tribe Clinical Research —Greenville, SC
- Full-time
- Blood sampling
- Computer literacy
- Writing skills
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Peer Recovery Coordinator, Emergency Department, Full Time, Evening
Prisma Health —Greenville, SC
- Full-time
- Addiction Medicine
- Word processing
- Computer literacy
Social Worker-Healthy Start FT, Day
Prisma Health —Greenville, SC
- Full-time
- Hospital
- Computer literacy
- Mid-level
Mental Health Therapist - South Carolina (Part-Time)
Two Chairs —Greenville, SC
- $58.50 - $85.00 an hour
- Part-time
- Remote
- LMFT
- LPC
- HIPAA
- Continuing education credits
- 401(k)
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Director, Mobile Response and Stabilization Services - LPCC-S or LISW-S
Coleman Health Services —Marion, OH
Valid driver's license and maintain excellent driving record. Master's degree in counseling, social work, or a related field.
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Director of Behavioral Health (LISW-S, LPCC-S)
Coleman Health Services —Marysville, OH
Administrative and clinical supervision of our behavioral health staff. Experience in budgeting and/or program evaluation is also preferred.
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Stroke Research Coordinator II, Administrative Research, FT Days

Prisma Health -
Greenville, SC

Apply Now

Job Details

Full-time

Qualifications

Data quality checks
Clinical study protocols and reports
Academic research projects
Data quality assurance
Bachelor's degree in business
Mid-level
Collaborative research
Bachelor's degree in health sciences
Clinical staff training
Bachelor's degree
Team training
Data quality monitoring
Health Science
Compliance documentation
Quality compliance management
Medical record abstraction
Clinical trial patient safety management
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
Progress management
Collaborative Institutional Training Initiative Certification (CITI)
Progress documentation
Research participation
Business
Pharmaceutical research experience
Medical terminology
2 years
Documentation reviews
Medical literature reviews

Full Job Description

Inspire health. Serve with compassion. Be the difference.

Job Summary

Responsible for the implementation and day-to-day management of clinical trial research studies, including educating research staff, health care team members, participants, and caregivers. Coordinates the collection, submission, and oversight of clinical data; monitors protocol compliance; and maintains systems to support accurate and timely data flow. Manages participant visits and carries out protocol required procedures. Monitors participant progress and safety, and communicates relevant updates to investigators, regulatory offices, the health care team, and study staff.

Essential Functions

All team members are expected to be knowledgeable and compliant with Prisma Health's purpose: Inspire health. Serve with compassion. Be the difference.
Manages study operations by coordinating day today study operations and developing strategies to contribute to the program growth.
Monitors study progress and maintains compliance with protocols and regulations
Supports investigator-initiated studies by assisting with protocol development, literature reviews, and creation of data collection tools. Coordinates industry sponsored clinical trials by implementing sponsor provided protocols, completing required regulatory submissions, and ensuring adherence to study procedures and timelines.
Assists in coordinating resources to conduct trials including the development of data collection tools and communication with ancillary departments to implement study related procedures.
Collaborates with Research Services offices and sponsoring or local agencies to submit required study documents and ensure awareness of study progress, amendments, and regulatory activities.
Performs other duties as assigned.

Supervisory/Management Responsibilities

This is a non-management job that will report to a supervisor, manager, director or executive.

Minimum Requirements

Education - Bachelor's Degree in Health Sciences or Business-related field of study.
Experience - Two (2) years of research experience in at least one of the following areas: pharmaceutical, academic, device, National Institute of Health (NIH), investigator-initiated studies or registry trials.

In Lieu Of

In lieu of education and experience noted above an equivalent combination of work experience and academic experience may be considered.

Required Certifications, Registrations, Licenses

BLS is required within six (6) months of employment.
Collaborative Institutional Training Initiative (CITI) preferred.
If Allied Health Degree: State certification/license in field.
Some team members may be required to have a valid driver’s license to perform the essential functions of the role. In these situations, an acceptable motor vehicle record as defined by the Acceptable Motor Vehicle Record (MVR) Chart, and proof of auto insurance is required.

Knowledge, Skills and Abilities

Ability to apply Good Clinical Practice (GCP) principles independently across studies
Knowledge of clinical research regulations to daily operations
Ability to apply protocol requirements and troubleshoot visit issues
Ability to effectively use specialty‑specific terminology
Ability to independently interpret medical records with minimal assistance
Ability to independently manage quality data abstraction and ensure high-quality source documentation standards
Ability to maintain ongoing professional development by participating in seminars, workshops, in-service trainings, and by staying current with relevant literature and emerging trends in the field.

Work Shift

Day (United States of America)

Location

Greenville Memorial Hospital

Facility

2507 Upstate Administrative Research Staff

Department

25071000 Upstate Administrative Research Staff-Practice Operations

Share your talent with us! Our vision is simple: to transform healthcare for the benefits of the communities we serve. The transformation of healthcare requires talented individuals in every role here at Prisma Health.

Apply Now

Refine Your Search

clinical data manager jobs in greenville sc

Stroke Research Coordinator II, Administrative Research, FT Days

Operations - Site Lead

Peer Recovery Coordinator, Emergency Department, Full Time, Evening

Social Worker-Healthy Start FT, Day

Mental Health Therapist - South Carolina (Part-Time)

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