Top 25 Clinical research Jobs in Flat Rock, Nc

Clinical Research Assistant
ECN Operating LLC —Asheville, NC
- $20 - $22 an hour
- Full-time
- Ability to sit for extended periods
- Ability to stand for extended periods
- Communication skills
Quick Apply
Sr. Clinical Team Manager - FSP
Thermo Fisher Scientific —North Carolina
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- English
3d
FSP Country Approval Specialist
Thermo Fisher Scientific —North Carolina
- Full-time
- Remote
- Computer literacy
- English
- Mid-level
Global Study Lead - FSP Team
Thermo Fisher Scientific —North Carolina
- Full-time
- Remote
- Office
- Bachelor's degree
- Conflict management
Research Registered Nurse
American Oncology Network, Inc. —Asheville, NC
- $26.54 - $49.29 an hour
- Full-time
- Nursing
- Microsoft Outlook
- RN License
Quick Apply
Clinical Research Coordinator I - Nurse
Iterative Health —Asheville, NC
- Nursing
- RN License
- Quality control
Quick Apply
2d
Community-Based Participatory Research Fellow
Furman University —Greenville, SC
- Full-time
- University
- Doctor of Philosophy
- Mentoring
Breast Medical Oncology Physician
Mission Hospital —Asheville, NC
- Full-time
- Senior level
- Dental insurance
- 401(k)
Clinical Director- Project CARA
MAHEC —Asheville, NC
- Weekends as needed
- Medicine
- Microsoft Excel
- 3 years
- Loan forgiveness
Mgr, Clinical Vendor and Site Contracts
Lotus Clinical Research —United States
- $85,000 - $95,000 a year
- Full-time
- Remote
- Customer service
- 5 years
- Mid-level
Quick Apply
MedTech Part Time Clinical Consultant – San Francisco, CA
IQVIA —United States
- $85 an hour
- Part-time
- RN License
- Mid-level
- 3 years
MedTech Part Time Clinical Consultant – East Bay, San Francisco, CA
IQVIA —United States
- $85 an hour
- Part-time
- RN License
- Mid-level
- 3 years

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Clinical - Clinical Research Coordinator
Tribe Clinical Research —Greenville, SC
Trains other clinical trial associates making sure all individuals are up to date on all aspects of a clinical trial. Participate in weekly site meetings.
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Clinical Research Coordinator I (Temp Position Tentatively July 20, 2026-July 20, 2027)
Shriners Hospitals for Children —Greenville, SC
Bachelor's degree in clinical research, science or other healthcare field. Master's degree in related field. The Clinical Research Coordinator I is a research…
$21.74 - $32.62 an hour
Quick Apply

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Lab Services Coordinator - Clinical Trials Processing Lab
The Ohio State University Wexner Medical Center —Columbus, OH
Participates in data entry and management, quality control, audits and FDA inspections, continuous quality improvement and inventory management of clinical…
Financial Operations Analyst - Clinical Research
The Ohio State University Wexner Medical Center —Columbus, OH
This position is committed to developing comprehensive budgets and financial analysis of clinical trial projects, which incorporate knowledge and understanding…

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clinical research jobs near flat rock, nc

Clinical Research Assistant

ECN Operating LLC
Asheville, NC

Quick Apply

Job Details

Full-time
$20 - $22 an hour

Qualifications

Communication skills
Entry level
Time management

Full Job Description

Position Summary
The Research Assistant supports the execution of clinical research studies by performing
administrative, technical, and participant-focused tasks under the supervision of the
Clinical Research Coordinator and Principal Investigator. This role plays a critical part in
ensuring high-quality data collection, regulatory compliance, and participant safety. The
Research Assistant works collaboratively with the clinical team to facilitate study activities
in accordance with Good Clinical Practice (GCP) guidelines, study protocols, and
institutional policies.

Key Responsibilities
Study Support & Coordination

Assist in preparing study materials, source documents, and regulatory binders.
Support participant screening, recruitment, and scheduling in accordance with study protocols.
Maintain accurate participant logs and assist in tracking enrollment progress.
Ensure study areas, supplies, and equipment are organized and ready for study visits.

Data & Documentation

Accurately record data from source documents into electronic case report forms (eCRFs) or databases.
Maintain confidentiality and integrity of participant data in compliance with HIPAA and institutional standards.
Assist in resolving data queries and ensuring timely data entry.
Support document management, filing, and archiving according to regulatory requirements.

Participant Interaction

Greet and assist study participants during visits to ensure a positive experience.
Prepare consent materials and provide administrative support during the informed consent process.
Escort participants to appropriate testing areas and assist clinical staff with noninvasive study procedures as directed.

Regulatory & Compliance

Follow Good Clinical Practice (GCP) and institutional policies at all times.
Support compliance with IRB, sponsor, and regulatory agency requirements.
Participate in site audits, monitoring visits, and internal quality reviews as needed.

Team Collaboration

Work closely with Clinical Research Coordinators, Principal Investigators, and site teams to ensure timely completion of study milestones.
Participate in team meetings, training, and continuing education to stay current with study and regulatory updates.
Contribute to process improvements and operational efficiency initiatives.

Qualifications

Associate or bachelor’s degree in a health sciences, biology, psychology, or related field preferred.
Previous experience in healthcare or research setting is strongly preferred.
Familiarity with clinical trials, GCP, HIPAA, and human subjects research regulations are desirable.
Strong organizational, communication, and time management skills.
Ability to work accurately in a fast-paced environment with strong attention to detail.
Proficiency with Microsoft Office and data entry systems; experience with EDC or CTMS systems a plus.

Core Competencies

Accuracy and Attention to Detail
Professionalism and Confidentiality
Team Collaboration
Adaptability and Initiative
Ethical Conduct and Compliance Awareness

Physical Requirements

Ability to sit or stand for extended periods.
May require occasional lifting of study materials (up to 25 lbs).
Ability to interact with participants and staff in clinical and office settings.

Quick Apply

Refine Your Search

clinical research jobs in flat rock, nc

Clinical Research Assistant

Sr. Clinical Team Manager - FSP

FSP Country Approval Specialist

Global Study Lead - FSP Team

Research Registered Nurse

Clinical Research Coordinator I - Nurse

Community-Based Participatory Research Fellow

Breast Medical Oncology Physician

Clinical Director- Project CARA

Mgr, Clinical Vendor and Site Contracts

MedTech Part Time Clinical Consultant – San Francisco, CA

MedTech Part Time Clinical Consultant – East Bay, San Francisco, CA

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