1156 Lcsw jobs in Wilmington,NC

Licensed Clinical Social Worker

Headway

Wilmington, NC

Licensed Clinical Social Worker
You're a fully-licensed Clinical Social Worker at a Master's level or above with LCSW, LICSW, or LCSCW licensure (accepted on a state by state basis), a valid NPI number, and malpractice insurance.
You're ready to launch a private practice, or grow your existing business by taking insurance.
Please note: At this time, Headway can't support mental health professionals that aren't fully licensed. If your application was rejected for incomplete licensure, you're welcome to reapply once you have a valid license.

AB Staffing Solutions

Wilmington, NC 28412

Novant Health

Wilmington, NC 28401

High School Diploma or GED, required.
Minimum of three years in a critical care or healthcare equivalent setting, required.
OR/PACU required.
Current RN licensure in appropriate state, required.
Strong background in patient centric care;
Experience with facilitating education and training;
Must have the ability to complete assignments required for Medicare, JCAHO and other required organizations.
Proficient in Microsoft Office, particularly WORD, Excel and Outlook.
Experience in leadership roles;
Strong ethical and moral character references;
Language skills adequate for high-level written, interpersonal, and telephone communication.
Accuracy and attention to detail without compromise of patient care.

United States Army

Navassa, NC 28451

SonderMind Careers

Wilmington, NC 28412

Well Care, LLC

Wilmington, NC 28403

Thermo Fisher Scientific

Wilmington, NC

Education / Certifications: Life science or medical graduate or other relevant qualifications.
Minimum: CRA graduated
Experience: Relevant experience of pharmaceutical drug development: Experience of minimum 1 year (ideally 2 years) of Lead CRA e.g. coordination of clinical activities/site management activities for the set up and running of international registrational studies (multiple sites/countries).
Experience as a Field CRA monitor for at least 3 years (CROs or Pharma Industry)
Experience in Phase I Oncology
Excellent Knowledge of Good Clinical Practice (GCP), ICH regulations.
Experience in preparing clinical study documentation for study set up, maintenance and closing
Experience in managing and developing relationships with Contract Research Organizations (CROs). Global studies (multiple countries/sites) experience
Languages: English: Strong intermediate level