Top 22 Clinical specialist Jobs in Wilmington Nc

Clinical Research Site Startup Consultant/Site Activation Specialist
Coastal Internal Medicine —Wilmington, NC
- $100 an hour
- Part-time
- Management
- HIPAA
- Mid-level
Quick Apply
Robotics Clinical Sr Sales Rep
Zimmer Biomet —Wilmington, NC
- $100,000 - $120,000 a year
- Full-time
- Up to 50% travel
- Marketing
- Mid-level
- Wellness program
13d
Clinical Research Associate (Level II) - FSP - Alzheimer's - Central
Thermo Fisher Scientific —Wilmington, NC
- Full-time
- Nursing
- RN License
- Writing skills
14d
Licensed Clinical Addiction Specialist
EMPOWER HEALTH GROUP LLC —Wilmington, NC
- Part-time
- Addiction Medicine
- Mid-level
- Psychology
Quick Apply
14d
Certified Nursing Assistant
US Pediatric Partners —Wilmington, NC
- Customer service
- HIPAA
- High school diploma or GED
- Disability insurance
- Dental insurance
Quick Apply
Clinical Nurse Liaison - Palliative Care
Lower Cape Fear LifeCare —Wilmington, NC
- Weekends as needed
- Nursing
- RN License
- Marketing
Quick Apply
Clinical Nurse Liaison - Inpatient
Lower Cape Fear LifeCare —Wilmington, NC
- Weekends as needed
- Nursing
- RN License
- Hospital
Quick Apply
8d
Regional Clinical Reimbursement Consultant – State Veterans Homes
STG International, Inc. —Wilmington, NC
- Nursing
- Skilled nursing facility
- RN License
- Health insurance
- Dental insurance
Quick Apply
Licensed Clinical Psychologist
Clarity Counseling Center —Wilmington, NC
- $75 - $100 an hour
- Part-time
- Hybrid work
- Background check
- Private practice
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Hospice Clinical Nurse Liaison
Lower Cape Fear LifeCare —Wilmington, NC
- Weekends as needed
- Nursing
- RN License
- Public speaking
Quick Apply
Clinical Nurse
Tuba City Regional Health Care Corp —United States
- $32 - $50 an hour
- Full-time
- Nursing
- RN License
- Bachelor of Science
- Paid holidays
- Relocation assistance
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MedTech Part Time Clinical Consultant – San Francisco, CA
IQVIA —United States
- $85 an hour
- Part-time
- RN License
- Mid-level
- 3 years

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Clinical Research Site Startup Consultant/Site Activation Specialist

Coastal Internal Medicine -
Wilmington, NC

Quick Apply

Job Details

Part-time | Contract
$100 an hour

Qualifications

Statistical software
Statistics
Phase II clinical trials
Management
Healthcare staff management
HIPAA
Analysis skills
Budget planning
Data management
Attention to detail
Clinical information systems
CDISC standards
Clinical staff recruitment
Organizational skills
Clinical trial standard operating procedures
Adaptive clinical trial design
Patient recruitment
Clinical documentation improvement
Good Clinical Practice (GCP)
Medical terminology
FDA regulations
Research compliance quality assurance records management

Full Job Description

The primary objective of this position is to build the research site from startup through activation and enrollment of the first study participant.

Overview
We are seeking an experienced Clinical Research professional to help launch a new clinical research site. Responsibilities include developing SOPs, assisting with regulatory compliance and IRB submissions, setting up CTMS/eSource systems, hiring and training staff, establishing site operations, preparing for sponsor and CRO partnerships, supporting participant recruitment strategies, and ensuring ICH-GCP compliance. Experience in clinical research operations, site management, or study coordination is preferred. Strong organizational, leadership, and communication skills are required. This is an exciting opportunity to help build a research site from the ground up.

Duties

Lead the establishment of a new clinical research program within an existing internal medicine practice. Develop and implement Standard Operating Procedures (SOPs) compliant with ICH-GCP and FDA regulations. Establish regulatory, quality, and operational workflows for the research site. Prepare the site for sponsor/CRO qualification and site initiation visits. Select and implement CTMS, eRegulatory, eSource, and other research systems. Develop source document, regulatory, and essential document processes. Identify, evaluate, and implement required vendors (central laboratory, pharmacy, imaging, ECG, etc.). Assist with feasibility questionnaires, sponsor/CRO outreach, and obtaining the site's initial clinical trials. Support negotiation of clinical trial budgets and contracts with sponsors and CROs. Hire, train, and mentor clinical research staff. Ensure compliance with FDA regulations, ICH-GCP, IRB requirements, and applicable state and federal regulations. Develop participant recruitment strategies and operational plans to achieve enrollment goals. Provide ongoing operational guidance through the site's first patient enrollment.

Qualifications

Must have successfully helped establish one or more independent clinical research sites from startup. Experience obtaining a site's first sponsor/CRO studies. Experience developing SOPs, regulatory systems, and research workflows. Experience with IRB submissions, FDA/GCP compliance, and Essential Documents. Experience negotiating clinical trial budgets and contracts. Experience hiring and training Clinical Research Coordinators. Experience preparing sites for qualification, initiation, and sponsor audits. Strong network with CROs and sponsors preferred.

Proven supervising experience within a clinical research setting or healthcare environment
Strong understanding of medical terminology, clinical laboratory procedures, and healthcare compliance standards
Experience with data management systems, EMR platforms, and statistical software used in clinical research analysis
Knowledge of FDA regulations, ICH GCP guidelines, CDISC standards, and clinical ethical guidelines for research trials
Demonstrated ability to review complex documentation accurately and efficiently
Familiarity with project management principles in healthcare or research projects; certification in project management is a plus
Clinical development experience including trial design, patient safety monitoring, and regulatory submissions
Certification such as ICH GCP certificate from a recognized issuer (e.g., CA) is highly desirable
Excellent organizational skills with attention to detail; ability to multitask in a fast-paced environment
Strong communication skills to collaborate effectively with multidisciplinary teams including nurses, physicians, regulatory bodies, and sponsors
Join us in advancing healthcare through innovative research! We are committed to fostering a vibrant work environment that values your expertise while supporting your professional growth. This paid position offers an engaging opportunity to make meaningful contributions to clinical science while working alongside passionate professionals dedicated to improving patient outcomes.

Pay: $100.00 per hour

Application Question(s):

Have you personally helped establish a new independent clinical research site?
Briefly describe your role in launching the site, including SOP development, regulatory setup, sponsor qualification, and obtaining the first study.
How many independent clinical research sites have you personally helped establish?

Experience:

Site Start Up : 3 years (Required)

Work Location: In person

Quick Apply

Refine Your Search

clinical specialist jobs in wilmington nc

Clinical Research Site Startup Consultant/Site Activation Specialist

Robotics Clinical Sr Sales Rep

Clinical Research Associate (Level II) - FSP - Alzheimer's - Central

Licensed Clinical Addiction Specialist

Certified Nursing Assistant

Clinical Nurse Liaison - Palliative Care

Clinical Nurse Liaison - Inpatient

Regional Clinical Reimbursement Consultant – State Veterans Homes

Licensed Clinical Psychologist

Hospice Clinical Nurse Liaison

Clinical Nurse

MedTech Part Time Clinical Consultant – San Francisco, CA

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