Clinical Research Specialist
Clinical Research Coordinator Job 10 miles from Kernersville
Job Summary The Clinical Research Specialist is responsible for the coordination, collection, processing and quality control of clinical trial data under the direct supervision of the Manager Clinical Research. Maintains all research protocol data and compliance reporting.
Assists with screening patients for research protocol regimens.
Dedicated to excellence in all aspects of clinical research with a keen focus on ethics, safety, quality, compliance and stewardship.
Positions are primarily on-site, Monday through Friday.
Some positions may offer Hybrid work opportunities.
Come join a remarkable team where quality care meets quality service, in every dimension, every time.
#JoinTeamAubergine #NovantHealth Let Novant Health be the destination for your professional growth.
At Novant Health, one of our core values is diversity and inclusion.
By engaging the strengths and talents of each team member, we ensure a strong organization capable of providing remarkable healthcare to our patients, families and communities.
Therefore, we invite applicants from all group dynamics to apply to our exciting career opportunities.
Responsibilities It is the responsibility of every Novant Health team member to deliver the most remarkable patient experience in every dimension, every time.
Our team members are part of an environment that fosters team work, team member engagement and community involvement.
The successful team member has a commitment to leveraging diversity and inclusion in support of quality care.
All Novant Health team members are responsible for fostering a safe patient environment driven by the principles of "First Do No Harm".
Qualifications Candidates who meet any qualification level outlined below are encouraged to apply! Non-Nursing Levels: Clinical Research Specialist I Clinical Research Specialist II Clinical Research Specialist III No experience required.
Prefer previous experience in clinical research or healthcare setting such as Lab, billing, coding, insurance, phlebotomy, pharmacy, physician practices Minimum 5 years* of clinical or clinical research experience required.
2 years must be in clinical research Minimum 8 years* of clinical or clinical research experience required.
5 years must be in clinical research.
Certification in Clinical Research required.
* Education may count toward years of experience.
Accepted certifications in Clinical Research include the Association of Clinical Research Professionals (ACRP), the Society of Clinical Research Associates (SOCRA), Regulatory Affairs Professionals Society (RAPS) or Public Responsibility in Medicine and Research (PRIM&R).
Additional Skills (required): Must have exceptional organizational and analytical skills.
Self motivated and able to work independently.
Able to meet multiple deadlines for concurrent projects.
Work in a team-oriented setting.
Must have excellent computer skills and medical terminology competency.
• Must provide own transportation to clinics, hospitals and associated agencies as required.
• Manual dexterity, prolonged standing or sitting.
Able to lift light to medium weight objects which may be bulky and awkward.
• Ability to travel to developmental, educational and promotional activities.
• Physical and mental stamina required to function effectively in an environment with multiple fluctuating priorities.
• Ability to communicate effectively with individuals of diverse backgrounds and multiple levels of leadership.
• Exposure to hazardous materials (study agents, biohazards, pathology specimens).
Job Opening ID 44272
Clinical Studies Coordinator II, Gerontology
Clinical Research Coordinator Job 10 miles from Kernersville
Under departmental direction and in coordination with the Principal Investigator, the CSCII maintains various aspects of the iGROOVE study including oversight of participant recruitment and enrollment, regulatory monitoring and reporting, conducting study visits according to protocol to collect, compile and submit data, administer participant questionnaires, and oversight of other team members to manage day to day workflow. Ability to manage the workload of a study with increased complexity.
EDUCATION/EXPERIENCE
Bachelor's degree with two years' experience in clinical research; or an equivalent combination of experience and education.
LICENSURE, CERTIFICATION, and/or REGISTRATION
SOCRA or ACRP Certification preferred.
Must complete the CITI certification for Human Subject Research if not already completed.
All additional required WakeOne training for research coordinators.
ESSENTIAL FUNCTIONS
Works under the direction of the Study Investigators or departmental Manager with minimal supervision.
Plays an active role in recruitment of patients to study.
Performs protocol specific duties required per the research protocol.
Obtains or assists the Principal Investigator in obtaining informed consent from subjects and reinforces the information that has been provided to subjects and families.
Fulfills sponsor requirements related to reportable information including adverse events, unanticipated problems, and other information required by the sponsor protocol.
Abstracts data from the medical record and completes paper and electronic case report forms, including responding to any requests for data clarification, and maintains all necessary source documents.
Identifies and communicates important protocol and data management issues or problems to the supervisor in a timely manner.
Provides staff relief as required to meet the needs of the department. Participates in scheduled team/department meetings. Participates in quality improvement projects on an on-going basis.
May mentor new and less experienced staff.
Follows established institutional and department policies, procedures, objectives, performance improvement, attendance, safety, environmental, and infection control guidelines, including adherence to the workplace Code of Conduct and Compliance Plan. Practices a high level of integrity and honesty in maintaining confidentiality.
Performs other related duties as assigned or requested.
SKILLS/QUALIFICATIONS
Excellent interpersonal, oral, and written communication skills
Excellent reading comprehension
Strong organizational skills
EPIC/WakeOne proficiency to include appropriate documentation of research notes
Proficient in the use of OnCore/WISER Clinical Trial Management System
Basic computer skills
Fosters/promotes a positive image and professional appearance
Sensitivity to intercultural relations
Sensitivity to the maintenance of confidentiality
Knowledge of Microsoft Products
WORK ENVIRONMENT
Clean, comfortable, office environment
Clinical Studies Coordinator I, Comprehensive Cancer Center
Clinical Research Coordinator Job 10 miles from Kernersville
Under the direction of the Study Investigators and Disease Group Chair, mentorship of experienced clinical studies coordinator staff, supervision of the Nurse Team Leader and the leadership of the Director of Clinical Protocol and Data Management, the Clinical Studies Coordinator I coordinates activities to support research studies. Able to manage low complexity trials after completion of orientation. Assignments are gradually adjusted to add increased responsibility based on demonstrated competency. Mentored by an experienced clinical research coordinator II or III, serves as the principle administrative liaison for assigned studies. Follows and maintains recordkeeping systems and procedures to ensure compliance with study protocols and all appropriate regulations. Attends clinic as needed to perform activities including, but not limited to: assist the research team with recruitment activities, administer questionnaires, and answer any questions about future appointments. Responsible for the compilation, registration and submission of data, as required by the Sponsor.
Education/Experience:
Minimum Acceptable Qualifications:
Bachelor's degree in a related field of study or an equivalent combination of experience and education
Experience in a medical and/or research setting
Additional Desirable Qualifications:
Paramedical experience
Licensure, Certification and/or Registration:
SOCRA or ACRP certification preferred
Must complete the CITI certification for Human Subject Research if not already completed
All additional required WakeOne training for research coordinators
Essential Functions:
Study Conduct
Works under the supervision of the Study Investigators, Disease Group Chair and the direction of the Administrative Director of Clinical Protocol and Data Management.
Works in conjunction with a clinical studies coordinator mentor and the oversight of a Nurse Team Leader to gradually assume more responsibility and workload
Assists in the recruitment of patients to study by helping to identify potential eligible patients who are scheduled to be seen in the clinic and communicating the information to the Study Team.
Performs protocol specific duties required per the research protocol, including but not limited to:
Obtains or assists the Principal Investigator in obtaining informed consent from subjects and reinforces the information that has been provided to subjects and families.
Confirms and documents subject eligibility.
As part of the team, ensures all protocol procedures are ordered and completed as specified in the protocol.
Randomizes subjects using interactive voice response systems or other systems as applicable.
Administers standardized tools or questionnaires, such as Quality of Life assessments, if appropriately credentialed.
Assembles lab kits and other supplies in preparation to obtain required biospecimen samples and transports to appropriate laboratories for processing; ships samples externally per International Air Transport Association (IATA) requirements.
Optimizes the safety of research subjects by monitoring and reporting any adverse events to the investigators and other members of the study team.
Participates in required teleconferences, on site meetings and off site investigator meetings, as required.
Regulatory Compliance and Documentation.
Fulfills sponsor requirements related to reportable information, including: adverse events, unanticipated problems, other information required by the sponsor protocol.
Data Management
Abstracts data from the medical record and completes paper and electronic case report forms, including responding to any requests for data clarification, and maintains all necessary source documents.
Identifies and communicates important protocol and data management issues or problems to the supervisor in a timely manner.
Personnel Management
Provides staff relief as required to meet the needs of the department.
Participates in scheduled team/department meetings.
Participates in quality improvement projects on an on-going basis.
Follows established Wake Forest Baptist and department policies, procedures, objectives, performance improvement, attendance, safety, environmental, and infection control guidelines, including adherence to the workplace Code of Conduct and Compliance Plan. Practices a high level of integrity and honesty in maintaining confidentiality.
Performs other related duties as assigned or requested.
Skills and Qualifications:
Knowledge of medical terminology.
Exposure to clinical trials or related health field is preferred.
Excellent oral/written communication and organizational skills.
Excellent reading comprehension.
Foster/promote a positive image and professional appearance.
Sensitivity to intercultural relations.
Sensitivity to the maintenance of confidentiality.
Ability to use Microsoft products, access data in computer data bases, compile data, and research information.
Proofread documents.
Troubleshoot problems.
Clinical Studies Coordinator I, Comprehensive Cancer Center
Clinical Research Coordinator Job 10 miles from Kernersville
Under the direction of the Study Investigators and Disease Group Chair, mentorship of experienced clinical studies coordinator staff, supervision of the Nurse Team Leader and the leadership of the Director of Clinical Trials Office, the Clinical Studies Coordinator I coordinates activities to support research studies. Able to manage low complexity trials after completion of orientation. Assignments are gradually adjusted to add increased responsibility based on demonstrated competency. Mentored by an experienced clinical research coordinator II or III, serves as the principle administrative liaison for assigned studies. Follows and maintains recordkeeping systems and procedures to ensure compliance with study protocols and all appropriate regulations. Attends clinic as needed to perform activities including, but not limited to: assist the research team with recruitment activities, administer questionnaires, and answer any questions about future appointments. Responsible for the compilation, registration and submission of data, as required by the Sponsor.
EDUCATION/EXPERIENCE
Minimum Acceptable Qualifications:
Bachelor's degree in a related field of study or an equivalent combination of experience and education
Experience in a medical and/or research setting
Additional Desirable Qualifications:
Paramedical or other clinical experience
LICENSURE/CERTIFICATION
SOCRA or ACRP certification preferred
Must complete the CITI certification for Human Subject Research if not already completed
All additional required WakeOne training for research coordinators
ESSENTIAL FUNCTIONS
Study Conduct
Works under the supervision of the Study Investigators, Disease Group Chair and the direction of the Administrative Director of Clinical Trials Office.
Works in conjunction with a clinical studies coordinator mentor and the oversight of a Nurse Team Leader to gradually assume more responsibility and workload
Assists in the recruitment of patients to study by helping to identify potential eligible patients who are scheduled to be seen in the clinic and communicating the information to the Study Team.
Performs protocol specific duties required per the research protocol, including but not limited to:
Obtains or assists the Principal Investigator in obtaining informed consent from subjects and reinforces the information that has been provided to subjects and families.
Confirms and documents subject eligibility.
As part of the team, ensures all protocol procedures are ordered and completed as specified in the protocol.
Randomizes subjects using interactive voice response systems or other systems as applicable.
Administers standardized tools or questionnaires, such as Quality of Life assessments, if appropriately credentialed.
Assembles lab kits and other supplies in preparation to obtain required biospecimen samples and transports to appropriate laboratories for processing; ships samples externally per International Air Transport Association (IATA) requirements.
Optimizes the safety of research subjects by monitoring and reporting any adverse events to the investigators and other members of the study team.
Participates in required teleconferences, on site meetings and off site investigator meetings, as required.
Regulatory Compliance and Documentation
Fulfills sponsor requirements related to reportable information, including: adverse events, unanticipated problems, other information required by the sponsor protocol.
Data Management
Abstracts data from the medical record and completes paper and electronic case report forms, including responding to any requests for data clarification, and maintains all necessary source documents.
Identifies and communicates important protocol and data management issues or problems to the supervisor in a timely manner.
Personnel Management
Provides staff relief as required to meet the needs of the department.
Participates in scheduled team/department meetings.
Participates in quality improvement projects on an on-going basis.
Other
Follows established Wake Forest Baptist and department policies, procedures, objectives, performance improvement, attendance, safety, environmental, and infection control guidelines, including adherence to the workplace Code of Conduct and Compliance Plan.
Practices a high level of integrity and honesty in maintaining confidentiality.
Performs other related duties as assigned or requested.
SKILLS AND QUALIFICATIONS
Knowledge of medical terminology.
Exposure to clinical trials or related health field is preferred.
Excellent oral/written communication and organizational skills.
Excellent reading comprehension.
Foster/promote a positive image and professional appearance.
Sensitivity to intercultural relations.
Sensitivity to the maintenance of confidentiality.
Ability to use Microsoft products, access data in computer data bases, compile data, and research information.
Proofread documents.
Troubleshoot problems.
Clinical Research Specialist II
Clinical Research Coordinator Job 17 miles from Kernersville
The Clinical Research Specialist II position provides clinical support for research projects initiated and conducted by principal investigators. Under general supervision, this position works with study personnel to assist in completing and conducting subject follow-up visits.
Performs simple clinical tasks (e.g., obtaining vital signs) to support subject follow-up visits, and may perform more advanced tasks (i.e., electrocardiogram (ECG), pulmonary function tests (PFT), phlebotomy, drug administration, etc.).
Collects data from various sources, including patient charts, medical records, interviews, and diagnostic tests, and prepares comprehensive documentation, ensuring the accurate and reliable analysis of research data. Assists in the preparation and maintenance of study and subject-level documentation, reports, and other materials, keeping accurate records and organizing study materials efficiently, facilitating smooth research operations.
Provides support in proper research protocol compliance and development, including regulatory controls, study procedures, and data management, ensuring adherence to regulatory standards and promoting the reliability and validity of research outcomes. Supports the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory compliance necessary for research projects in the hospital/medical group setting.
Serves as study coordinator for studies with low risk to patients, such as registry and biospecimen collection studies, successfully coordinating site initiation visits, monitoring visits, and close-out visits, while ensuring adherence to protocol guidelines and regulatory requirements.
Recruits and screens prospective research participants and obtains informed consent from study participants.
Reviews new protocols for biological specimen requirements, ensures all necessary supplies are on-site, and prepares or oversees the preparation of biological specimens for shipment to reference laboratories, supporting the efficient and accurate analysis of research samples.
Prepares for site initiation, monitoring, and audit visits, supporting smooth and compliant research processes and maintaining a high standard of research conduct.
Performs other duties as assigned.
EDUCATION:Required: High school diploma or equivalent
EXPERIENCE:Required: 2 years clinical experience; 1 year clinical research experience including consenting patients.
LICENSURE/CERTIFICATION/REGISTRY/LISTING:Required: Healthcare/Health-related certification
Equal Opportunity Employer At Cone Health, we strive to create a welcoming atmosphere that celebrates a diverse and unique workforce. We believe in offering equal opportunities for employment to all applicants and employees, regardless of their race, religion, age, sex, sexual orientation, gender identity, veteran's status, ethnicity, national origin, disability, color, or any other characteristic protected by law. Our hiring and employment choices are based on each individual's qualifications, skills and performance. We believe that by embracing the diversity of our team, we can better serve our patients, communities and each other.
Senior Clinical Research Coordinator with Management Experience
Clinical Research Coordinator Job 10 miles from Kernersville
PETERS MEDICAL RESEARCH "Partnering with patients today for tomorrow's miracles!" "Established Clinical Research Company is seeking a Senior Clinical Research Study Coordinator with management experience to join our team in High Point!" Job Description * Complete QC of patient medical records and source documentation.
►Assist in managing all regulatory documents
►Assist with managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.
* Act as the primary point of contact for sponsors/CROs. Facilitate and coordinate monitoring visits.
* Support marketing activities, as needed.
* Maintain clinical research professional credentials.
Requirements
* Employee must be available during "core" clinic hours of 8:00 a.m. to 5:00 p.m., Monday through Friday with some flexibility to work from 1-3 hours on Saturday, if needed.
* This is not a remote position as it requires direct patient care in a clinical setting.
* 5+ years of Clinical Research experience is required
* Bachelor's Degree is required
* Master's Degree is preferred
* Management experience is required
* Phlebotomy certification is required
Skills
* Ability to collect patient vitals and ECGs.
* Knowledge of GCP and applicable government FDA regulations. Current GCP Certification preferred.
* Strong team player and quick to help resolve problems.
* Knowledgeable of medical and research terminology, laboratory sanitation, and safety guidelines.
* Friendly with patients and clinic staff. Great communication skills, including verbal, written, and personal.
* Proficient in MS Applications. Solid data entry skills. EMR and EDC database experience preferred.
* Extremely detail-oriented with a focus on quality. Capable of multi-tasking in a fast-paced clinic environment.
* Reliable and dependable to finish projects, deliverables, and tasks on time without close supervision.
* Outstanding organizational skills in managing paper and electronic documents.
Competitive Benefit Package Includes:
* Competitive Yearly Compensation (Compensation commensurate with experience)
* Medical/Dental/Vision
* Generous PTO
* Company Paid Holidays
* Company matched 401K Plan
* And more!
Peters Medical Research is affiliated with Bethany Medical:
Bethany Medical is the largest independent established multi-specialty group in Central North Carolina, serving the Triad and surrounding communities for over 35 years. Bethany Medical is open 7 days a week, with 13 convenient locations and 16 practices in Greensboro, Winston-Salem, High Point, Kernersville, Jamestown, North Wilkesboro, and Mt Airy, North Carolina. We have grown to provide the facilities, staff, and support to offer urgent care, primary care, diagnostic testing, outpatient ancillary, and specialty care services on-site. Bethany Medical is staffed with board-certified physicians and providers representing 16 medical specialties. Practice staff members are known for treating each patient with prompt personalized care and attention. Bethany Medical employs over 65 providers and over 525 employees.
About the Triad:
The Triad area includes Greensboro (3rd Largest City in NC), Winston Salem, High Point, and the surrounding area. The Triad is centrally located in NC with a population of 1.9 million. The Triad is 1 hour from the mountains and 3 hours from the beach. Charlotte and Raleigh are 1.5 hours from the Triad. The Triad offers all the amenities of a larger city without all the traffic. The Piedmont Triad International Airport is conveniently located in Greensboro with convenient non-stop flights to most major cities. Enjoy an outstanding quality of life with no shortage of arts, entertainment, recreation, shopping, and hundreds of restaurants. The Triad is home to 85 colleges and universities including Wake Forest University, High Point University, UNC-Greensboro, NC A&T, Guilford College, Bennett College, and Greensboro College.
#IND100
Research Consultant-Research Team-Medical & Scientific Solutions
Clinical Research Coordinator Job 17 miles from Kernersville
Womble Bond Dickinson (US) LLC is currently seeking a Research Consultant for the Medical & Scientific Solutions Team which will be responsible for conducting high level research on medical and. . .
Clinical Assistant/Associate Professor-Clinic Director
Clinical Research Coordinator Job 17 miles from Kernersville
Faculty in the Department of Counseling and Educational Development ( CED ) in the School of Education at the University of North Carolina at Greensboro ( UNCG ) seek a colleague who will provide stability and visionary leadership for the Nicholas A. Vacc Counseling and Consulting Clinic (Clinic) as the Clinic Director beginning August 1, 2025 . We are searching for a team-oriented, collaborative individual who will serve as Clinic Director and contribute their own experience, expertise, and commitment to the Department's equity, diversity, and inclusion initiatives through Clinic services. This is a 9-month, full-time, in-person position. This position is primarily focused on directing the Clinic and teaching at the masters or doctoral level, however, includes a reduced teaching load given the service as Clinic Director that this role entails. Review of applications will begin on October 1, 2024, and will continue until the position is filled. Salary for this position is competitive and contingent on experience. Key functions and expected performance: Working collaboratively with departmental faculty and staff to navigate the connections of current courses, course content, research, and practica experiences within the Clinic, as well as determining future directions of the Clinic. Teaching courses at the master's or doctoral level. Managing and organizing clinical experiences that occur within the Clinic, which includes but is not limited to adequate clinical hours for required clinical courses that occur within the Clinic and providing orientation to all Clinic policies and procedures. Maintaining and enhancing existing relationships with units on campus to provide services to UNCG students, and developing visionary strategies for the Clinic to expand its reach and influence in the schools and community. Providing on-site supervision and crisis consultation as needed during normal business hours for CED practicum and internship students and monitoring compliance with legal and ethical issues. Managing, supervising, and directing Clinic employees and graduate assistants who staff the Clinic and on-call schedule. Managing budgets, technology, and operations of the Clinic and engaging in data collection to assist in providing data and metrics regarding the Clinic's impact on and off campus. Providing departmental, school, and University service.
Minimum Qualifications
Candidates must hold or anticipate a doctorate in Counselor Education from a CACREP -accredited program. Candidates who have not yet received a doctoral degree but anticipate receiving the degree will be considered for this position. Candidates are required to have training in clinical supervision and successful experience as a clinical supervisor.
Preferred Qualifications
Applicants should have, or be eligible for, relevant counselor credentials (e.g., LCMHC -S, LCMHC , NCC ) in North Carolina. Clinical supervision credentials (e.g., LCMHC -S, ACS ) are preferred. Candidates should have training and/or clinical experience in providing telemental health services.
Work Environment
Inside - C
Licensed Clinical Practitioner/ Associate
Clinical Research Coordinator Job 17 miles from Kernersville
The Licensed Practitioner is responsible for : Conducting Assessments of consumers Conducting Outpatient therapy Conducting Intakes Submitting clients for Reauthorization Conducting Group sessions Complete updates as neccessary for client's file Working with both populations Adults and Adolescence
Provide screening and therapeutic consuling to consumers
Assisting in other areas that is required by the agency
Qualifications
Licensed Clinical Practitioner must have Masters Degree in Human Services field with at least one year documented experience in mental health and/or substance abuse.
Licensed Practitioner must maintain valid CPR, TB Skin Test, Medication Management, BBP, NCI or training on Alternative to Restictive Intervention. Licensed Practitioner must maintain trainings required by board.
Additional Information
All your information will be kept confidential according to EEO guidelines.
Instructor/Clinical Coordinator, Radiography
Clinical Research Coordinator Job 12 miles from Kernersville
Job Title Instructor/Clinical Coordinator, Radiography Status Regular Full Time/Part Time Full-time Location Job Description At Guilford Technical Community College (GTCC), we are dedicated to transforming lives through education and creating a lasting impact on our community. We invite passionate and innovative educators to join our mission-driven team, where you can enjoy a fulfilling work-life balance and competitive benefits, including a robust pension plan. Our beautiful, well-maintained campuses provide an inspiring environment for both teaching and learning, within an atmosphere of collaboration and excellence. At GTCC, you'll be part of a supportive, dynamic, and inclusive culture committed to delivering exceptional results, making it a truly amazing place to work and thrive.
The Radiography Clinical Coordinator/Instructor works in collaboration with the Radiography Program Director and the Dean of Health Sciences, to ensure a robust and relevant clinical experience for program students, including recruiting new clinical sites and fostering existing clinical relationships. This position also provides clinical and didactic instruction, customer service, data support, and documentation services in accordance with state and college regulations as well as external accreditation standards. The full-time faculty member is afforded some administrative release time to carry out clinical coordinator duties.
Min Salary Mid Salary Duties/Functions Difficult Challenges Contacts Education Required
* Bachelor's degree in Radiography or Radiologic Technology or a related field of study from an institutionally accredited post-secondary institution.
* Current American Registry of Radiologic Technologists (ARRT) certification and registration, or equivalent, in radiography.
Education Preferred Experience Required
* Three (3) years experience in radiography clinical practice.
* One (1) year experience instructing radiography students enrolled in a JRCERT accredited program.
Experience Preferred KSA Required
The Instructor as Clinical Coordinator of the Radiography Program shall possess an understanding of and commitment to the nature and role of the Community College, particularly its "open door" policy. He/she shall have demonstrated personal and professional competence for the responsibilities assigned. The Radiography Clinical Coordinator Instructor will have an understanding of the concept of a learning-centered, open admissions institution, community college philosophy, diversity issues, and instructional technology. The Radiography Clinical Coordinator Instructor must be able to:
1. Respect Diversity
2. Adapt to changing procedures, protocols, or assignments
3. Create and maintain a learner centered environment
4. Communicate effectively
5. Ability to effectively implement and apply technology solutions
6. Strategically think and manage change
7. Initiate, develop, and maintain relationships internal and external to the College
KSA Preferred Department/Job Specific Requirements
* Eligible to work with students in clinical settings and have access to student images for educational purposes.
* Have communication skills as a liaison for the program with radiography staff in clinical settings and with students
* Willing and able to travel to clinical sites.
* Learn program assessment tools and clinical documentation system (Trajecsys).
* Schedule may require day or evening responsibilities and travel between campuses as required for performance of job duties.
* Responsibilities may include overnight travel in and outside of the state, in support of college programs and initiatives.
Physical Demands Posting Type Faculty
Clinical Associate-Nights
Clinical Research Coordinator Job 41 miles from Kernersville
*Sovah Martinsville* *Who We Are:* *People are our passion and purpose.* Come to work where you are appreciated for who you are not just what you can do. Licensed for 220 beds, SOVAH Health - Martinsville, is a full-service, acute-care hospital providing over 22 medical specialties. Among the services we offer are a home health & hospice agency, advanced wound healing center, cardiac rehabilitation center, two cardiac catheterization labs, and medical & radiation oncology services.
*Where We Are:*
In Martinsville, explore culture and arts, enjoy kayaking or hiking and so much more in the foothills of the Blue Ridge Mountains. From the river to the racetrack, we offer plenty of activities to guarantee that you and your family have a fun-filled time!
*Why Choose Us:***
· Health (Medical, Dental, Vision) and 401K Benefits for full-time employees
· Competitive Paid Time Off / Extended Illness Bank package for full-time employees
· Employee Assistance Program - mental, physical, and financial wellness assistance
· Tuition Reimbursement/Assistance for qualified applicants
· Professional development, Growth Opportunities, and Mentor-based training
· And much more...
*Position Summary:***
Sovah Martinsville is seeking a full-time Clinical Associate to join our night shift team (7p - 7a & EOW).
The CA will provide direct and indirect patient care under the direction of a registered nurse and/or physician and will provide personal care, and comfort assistance with a safe, clean environment, and maintain equipment and supplies. Under the supervision of an RN, performs basic patient care activities.
* Performs basic patient care activities as delegated and supervised by an RN, including obtaining and recording vital signs, including blood pressure, pulse, respiration, and temperature as directed.
* Assists patients with tending to personal care and activities of daily living, including but not limited to bathing, grooming, eating, and ambulation.
* Reports abnormal findings or changes in physical, mental, and emotional conditions to nursing staff.
* Assists with keeping patient rooms and common areas stocked, clean, and orderly.
* Assists patients in the use of toilet facilities, including bedpans.
* Assists patients with ambulation, including the use of walkers and wheelchairs, when applicable.
* Assists patients with feeding, when needed.
* Assists patient with fluid intake, as directed, and measures and records fluid intake and output.
* Repositions patient, as appropriate.
* Checks diapers/under pads with each position change and ensures patient cleanliness; provides linen change as needed.
* Utilizes proper patient identification system, i.e. two patient identifiers.
*Minimum Education:*
* High school diploma or equivalent required.
*Required Skills:*
* Requires critical thinking skills, decisive judgment, and the ability to work with minimal supervision.__
* Must be able to work in a stressful environment and take appropriate action.__
* Requires ability to read and write legibly and carry out directions promptly and accurately.__
* Must exhibit effective communication skills and interpersonal skills.__
* Must be able to demonstrate the knowledge and skills necessary to provide care appropriate to the age of the patients served.__
* Requires the ability to respond quickly and calmly under stressful or emergencies.__
* Requires flexibility in scheduling and ability to work all shift patterns including weekends and holidays to ensure continuity of care and appropriateness of nursing coverage to the patients of Sovah Health Danville on all units.__
**
*Required Certifications/Licenses:*
* AHA Basic Life Support (BLS) required.
**
*Minimum Work Experience:*
* One (1) year as a CNA, Respiratory Care Assistant, Rehab Tech, Certified Medical Assistant, EKG Tech, EMT, Phlebotomist, or equivalent clinical experience preferred.
*EEOC Statement:*
SOVAH Health - Martinsville is committed to providing Equal Employment Opportunities for all applicants and employees and complies with all applicable laws prohibiting discrimination against any employee or applicant for employment because of color, race, sex, age, religion, national origin, disability, genetic information, gender identity, sexual orientation, veterans' status or any other basis protected by applicable federal, state or local law.
**Job:** **Nursing/Medical Assistant*
**Organization:** **Sovah Health - Martinsville*
**Title:** *Clinical Associate-Nights*
**Location:** *Virginia-Martinsville*
**Requisition ID:** *7455-13058*
Clinical Studies Coordinator II, Gerontology
Clinical Research Coordinator Job 10 miles from Kernersville
Under departmental direction and in coordination with the Principal Investigator, the CSCII maintains various aspects of the iGROOVE study including oversight of participant recruitment and enrollment, regulatory monitoring and reporting, conducting study visits according to protocol to collect, compile and submit data, administer participant questionnaires, and oversight of other team members to manage day to day workflow. Ability to manage the workload of a study with increased complexity.
EDUCATION/EXPERIENCE
Bachelor's degree with two years' experience in clinical research; or an equivalent combination of experience and education.
LICENSURE, CERTIFICATION, and/or REGISTRATION
SOCRA or ACRP Certification preferred.
Must complete the CITI certification for Human Subject Research if not already completed.
All additional required WakeOne training for research coordinators.
ESSENTIAL FUNCTIONS
Works under the direction of the Study Investigators or departmental Manager with minimal supervision.
Plays an active role in recruitment of patients to study.
Performs protocol specific duties required per the research protocol.
Obtains or assists the Principal Investigator in obtaining informed consent from subjects and reinforces the information that has been provided to subjects and families.
Fulfills sponsor requirements related to reportable information including adverse events, unanticipated problems, and other information required by the sponsor protocol.
Abstracts data from the medical record and completes paper and electronic case report forms, including responding to any requests for data clarification, and maintains all necessary source documents.
Identifies and communicates important protocol and data management issues or problems to the supervisor in a timely manner.
Provides staff relief as required to meet the needs of the department. Participates in scheduled team/department meetings. Participates in quality improvement projects on an on-going basis.
May mentor new and less experienced staff.
Follows established institutional and department policies, procedures, objectives, performance improvement, attendance, safety, environmental, and infection control guidelines, including adherence to the workplace Code of Conduct and Compliance Plan. Practices a high level of integrity and honesty in maintaining confidentiality.
Performs other related duties as assigned or requested.
SKILLS/QUALIFICATIONS
Excellent interpersonal, oral, and written communication skills
Excellent reading comprehension
Strong organizational skills
EPIC/WakeOne proficiency to include appropriate documentation of research notes
Proficient in the use of OnCore/WISER Clinical Trial Management System
Basic computer skills
Fosters/promotes a positive image and professional appearance
Sensitivity to intercultural relations
Sensitivity to the maintenance of confidentiality
Knowledge of Microsoft Products
WORK ENVIRONMENT
Clean, comfortable, office environment
Clinical Research Coordinator II
Clinical Research Coordinator Job 17 miles from Kernersville
The Clinical Research Coordinator II works closely with study subjects and other research staff and is responsible for the day-to-day clinical research process to collect, compile, document, and analyze clinical research data. Working under general supervision, the position conducts subject follow-up visits, completes clinical tasks, prepares research documentation, reports, and graphs while keeping appropriate logs, tracking participants, and preparing study materials.
Coordinates multiple clinical trials simultaneously or clinical trials with unique complexity, managing and organizing various research activities efficiently, ensuring optimal use of resources and timely execution of research protocols.
Assesses patients for protocol eligibility, ensuring the appropriate selection of participants for clinical trials, thereby enhancing the accuracy and validity of research outcomes. Confers with study participants to explain the purpose of the study and obtains informed consent, fostering transparency and trust with patients and their families throughout the research process.
Collects data from various sources, including patient charts, medical records, interviews, and diagnostic tests, and prepares comprehensive documentation, ensuring the accurate and reliable analysis of research data. When applicable, completes documentation in the electronic health/medical record (EMR) system to securely maintain patient health records.
Completes clinical tasks (i.e., ECGs, PFTs, phlebotomy, drug administration, etc.) when not prohibited by state or licensing board requirements under the supervision of the principal investigator.
Serves as study coordinator for pharmaceutical and/or device trials, successfully coordinating site initiation visits, monitoring visits, and close-out visits, and ensuring adherence to protocol guidelines and regulatory requirements.
Supports the regulatory process in the submission of study protocols, consent forms, and recruiting materials to the Institutional Review Board and the department for approval, facilitating the regulatory compliance necessary for research projects in the hospital/medical group setting.
Mentors and trains Clinical Research Coordinators and Clinical Research Specialists to ensure an effective and compliant team.
Performs other duties as assigned.
EDUCATION:Required: Associate degree with 4 years of Clinical Research experience OR Bachelor's degree with 2 years of clinical research experience
EXPERIENCE:Required: 6 years (education and/or experience)
LICENSURE/CERTIFICATION/REGISTRY/LISTING:Required: Clinical Research Coordinator (CCRC) and/or Clinical Research Associate (CCRA) certification
Equal Opportunity Employer At Cone Health, we strive to create a welcoming atmosphere that celebrates a diverse and unique workforce. We believe in offering equal opportunities for employment to all applicants and employees, regardless of their race, religion, age, sex, sexual orientation, gender identity, veteran's status, ethnicity, national origin, disability, color, or any other characteristic protected by law. Our hiring and employment choices are based on each individual's qualifications, skills and performance. We believe that by embracing the diversity of our team, we can better serve our patients, communities and each other.
Clinical Research Diet Coordinator, Clinical and Translational Science Institute
Clinical Research Coordinator Job 10 miles from Kernersville
Under administrative review, the clinical research diet coordinator performs management level work directed toward the planning, development, implementation, and evaluation of dietary/nutrition protocols associated with departmental research. Responsible for providing guidance and direction to a diverse group of nutrition staff including Registered Dietitians.
The Clinical Research Diet Coordinator is a key operational leader that oversees CTSI's Clinical Research Unit Bionutrition team and services. This leader provides overall supervision of Registered Dietitian Coordinator(s) and the Metabolic Kitchen supervisor and staff. The Diet Coordinator works with faculty and study teams in planning and implementing nutrition-based studies. This role is also responsible for the following: assistance in planning, preparation, and presentation of research proposals; directs and participates in the collection of dietary data for research purposes; directs, monitors, and participates in the counseling of study participants; serves as nutrition consultant to faculty and dietitian staff in evaluating and/or writing dietary components of research protocols.
EDUCATION/EXPERIENCE
Bachelor's degree with seven years' relevant experience required.
Master's degree in Human/Clinical Nutrition, Public Health, or Health Education preferred.
New licensing guidelines require a Master's Degree in order to become a RD
Five years' relevant clinical and/or administrative experience in health-related positions or research projects involving dietary assessment and dietary intervention, and/or food service required.
Supervisory ability required.
Experience in both single- and multi-center studies preferred.
LICENSURE, CERTIFICATION, and/or REGISTRATION
Professional registration by the Academy of Nutrition and Dietetics (AND) and licensure by the state of North Carolina Board of Dietetics/Nutrition (NCBDN) required.
ESSENTIAL FUNCTIONS
Provides overall supervision and direction to a group of nutrition staff members including dietitians. Responsible for the selection, training, direction, and evaluation of clinical research dietitians and dietary support staff assigned to research projects.
Participates in the planning, preparation, and presentation of research proposals or manuscripts, in collaboration with faculty members.
Major responsibility for tasks that result in the successful conduct and completion of assigned research projects involving dietary studies.
Coordinates continuing education seminars for research dietitians approved by the Academy of Nutrition and Dietetics (AND) for continuing education credits.
Translates planning and design decisions into concrete projects activities and establish priorities for implementation.
Directs and participates in the collection of dietary data for research purposes by employing effective, efficient, appropriate methodologies in accordance with study protocols.
Directs, monitors, and participates in the counseling of study participants individually or in groups to help them achieve the designated dietary specifications and food patterns consistent with goals of research protocols.
Serves as nutrition consultant to faculty and dietitian staff in evaluating and/or writing dietary component(s) of research protocols.
Develops specialized diets to achieve specific goals of research projects.
Manages the preparation of progress reports and quality control monitoring.
Attends and participates in national and local meetings related to study implementation.
Maintains professional status in accordance with the guidelines of the AND Council on Dietetic Registration (CDR).
Performs other related duties incidental to the work described herein.
SKILLS/QUALIFICATIONS
Excellent oral, written, and interpersonal communication skills
Knowledge of personal computers using word processing and spreadsheet software
WORK ENVIRONMENT
Clean, comfortable, office environment
Senior Clinical Research Coordinator with Management Experience
Clinical Research Coordinator Job 10 miles from Kernersville
PETERS MEDICAL RESEARCH
“Partnering with patients today for tomorrow's miracles!”
“Established Clinical Research Company is seeking a Senior Clinical Research Study Coordinator with management experience to join our team in High Point!” Job Description
· Complete QC of patient medical records and source documentation.
►Assist in managing all regulatory documents
►Assist with managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.
· Act as the primary point of contact for sponsors/CROs. Facilitate and coordinate monitoring visits.
· Support marketing activities, as needed.
· Maintain clinical research professional credentials.
Requirements
Employee must be available during “core” clinic hours of 8:00 a.m. to 5:00 p.m., Monday through Friday with some flexibility to work from 1-3 hours on Saturday, if needed.
This is not a remote position as it requires direct patient care in a clinical setting.
5+ years of Clinical Research experience is required
Bachelor's Degree is required
Master's Degree is preferred
Management experience is required
Phlebotomy certification is required
Skills
· Ability to collect patient vitals and ECGs.
· Knowledge of GCP and applicable government FDA regulations. Current GCP Certification preferred.
· Strong team player and quick to help resolve problems.
· Knowledgeable of medical and research terminology, laboratory sanitation, and safety guidelines.
· Friendly with patients and clinic staff. Great communication skills, including verbal, written, and personal.
· Proficient in MS Applications. Solid data entry skills. EMR and EDC database experience preferred.
· Extremely detail-oriented with a focus on quality. Capable of multi-tasking in a fast-paced clinic environment.
· Reliable and dependable to finish projects, deliverables, and tasks on time without close supervision.
· Outstanding organizational skills in managing paper and electronic documents.
Competitive Benefit Package Includes:
· Competitive Yearly Compensation (Compensation commensurate with experience)
· Medical/Dental/Vision
· Generous PTO
· Company Paid Holidays
· Company matched 401K Plan
· And more!
Peters Medical Research is affiliated with Bethany Medical:
Bethany Medical is the largest independent established multi-specialty group in Central North Carolina, serving the Triad and surrounding communities for over 35 years. Bethany Medical is open 7 days a week, with 13 convenient locations and 16 practices in Greensboro, Winston-Salem, High Point, Kernersville, Jamestown, North Wilkesboro, and Mt Airy, North Carolina. We have grown to provide the facilities, staff, and support to offer urgent care, primary care, diagnostic testing, outpatient ancillary, and specialty care services on-site. Bethany Medical is staffed with board-certified physicians and providers representing 16 medical specialties. Practice staff members are known for treating each patient with prompt personalized care and attention. Bethany Medical employs over 65 providers and over 525 employees.
About the Triad:
The Triad area includes Greensboro (3rd Largest City in NC), Winston Salem, High Point, and the surrounding area. The Triad is centrally located in NC with a population of 1.9 million. The Triad is 1 hour from the mountains and 3 hours from the beach. Charlotte and Raleigh are 1.5 hours from the Triad. The Triad offers all the amenities of a larger city without all the traffic. The Piedmont Triad International Airport is conveniently located in Greensboro with convenient non-stop flights to most major cities. Enjoy an outstanding quality of life with no shortage of arts, entertainment, recreation, shopping, and hundreds of restaurants. The Triad is home to 85 colleges and universities including Wake Forest University, High Point University, UNC-Greensboro, NC A&T, Guilford College, Bennett College, and Greensboro College.
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Research Consultant-Research Team-Medical & Scientific Solutions
Clinical Research Coordinator Job 10 miles from Kernersville
Womble Bond Dickinson (US) LLC is currently seeking a Research Consultant for the Medical & Scientific Solutions Team which will be responsible for conducting high level research on medical and. . .
Clinical Coordinator, Rehabilitation, Kernersville
Clinical Research Coordinator Job In Kernersville, NC
***PHYSICAL THERAPY LICENSE REQUIRED***
Provides clinical leadership and supervision of the care of patients in the designated work area. Develops administers, and coordinates therapy services in order to ensure positive patient outcomes. Provides comprehensive therapeutic patient care for neonatal, pediatric, adolescent, adult, and geriatric patients.
EDUCATION/EXPERIENCE:
Bachelor's degree in Physical Therapy from an accredited physical therapy school with two years' experience as a staff therapist in a clinical setting required.
Master's or Doctorate degree in Physical Therapy preferred.
One-year supervisory experience preferred.
LICENSURE, CERTIFICATION, and/or REGISTRATION:
Current licensure in the state of North Carolina and CPR certification in Basic Life Support, Level C required.
ESSENTIAL FUNCTIONS:
Provides patient care assessment and treatment.
Educates patients, significant others and other health care providers to assure continuity of the patient care plan.
Coordinates clinical operations for staff schedules and patient care processes.
Supervises therapy staff and students to develop their clinical skills and maintain the delivery of quality patient care. Serves as a role model for profession and clinical resource for staff.
Maintains accurate documentation.
Manages and facilitates quality care and growth of clinical staff.
Participates in process management to optimize quality and efficiency of patient care delivery.
Monitors and guides area to insure compliance with all internal and external professional and regulatory agency standards.
Promotes professional development and education of health care workers. Participates as a representative on committees.
Provides appropriate patient care in accordance with age/developmental guidelines.
Instructor/Clinical Coordinator, Radiography
Clinical Research Coordinator Job 12 miles from Kernersville
At Guilford Technical Community College ( GTCC ), we are dedicated to transforming lives through education and creating a lasting impact on our community. We invite passionate and innovative educators to join our mission-driven team, where you can enjoy a fulfilling work-life balance and competitive benefits, including a robust pension plan. Our beautiful, well-maintained campuses provide an inspiring environment for both teaching and learning, within an atmosphere of collaboration and excellence. At GTCC , you'll be part of a supportive, dynamic, and inclusive culture committed to delivering exceptional results, making it a truly amazing place to work and thrive. The Radiography Clinical Coordinator/Instructor works in collaboration with the Radiography Program Director and the Dean of Health Sciences, to ensure a robust and relevant clinical experience for program students, including recruiting new clinical sites and fostering existing clinical relationships. This position also provides clinical and didactic instruction, customer service, data support, and documentation services in accordance with state and college regulations as well as external accreditation standards. The full-time faculty member is afforded some administrative release time to carry out clinical coordinator duties.
Clinical Associate-Nights
Clinical Research Coordinator Job 41 miles from Kernersville
Sovah Martinsville Who We Are: People are our passion and purpose. Come to work where you are appreciated for who you are not just what you can do. Licensed for 220 beds, SOVAH Health - Martinsville, is a full-service, acute-care hospital providing over 22 medical specialties. Among the services we offer are a home health & hospice agency, advanced wound healing center, cardiac rehabilitation center, two cardiac catheterization labs, and medical & radiation oncology services.
Where We Are:
In Martinsville, explore culture and arts, enjoy kayaking or hiking and so much more in the foothills of the Blue Ridge Mountains. From the river to the racetrack, we offer plenty of activities to guarantee that you and your family have a fun-filled time!
Why Choose Us:
* Health (Medical, Dental, Vision) and 401K Benefits for full-time employees
* Competitive Paid Time Off / Extended Illness Bank package for full-time employees
* Employee Assistance Program - mental, physical, and financial wellness assistance
* Tuition Reimbursement/Assistance for qualified applicants
* Professional development, Growth Opportunities, and Mentor-based training
* And much more…
Position Summary:
Sovah Martinsville is seeking a full-time Clinical Associate to join our night shift team (7p - 7a & EOW).
The CA will provide direct and indirect patient care under the direction of a registered nurse and/or physician and will provide personal care, and comfort assistance with a safe, clean environment, and maintain equipment and supplies. Under the supervision of an RN, performs basic patient care activities.
* Performs basic patient care activities as delegated and supervised by an RN, including obtaining and recording vital signs, including blood pressure, pulse, respiration, and temperature as directed.
* Assists patients with tending to personal care and activities of daily living, including but not limited to bathing, grooming, eating, and ambulation.
* Reports abnormal findings or changes in physical, mental, and emotional conditions to nursing staff.
* Assists with keeping patient rooms and common areas stocked, clean, and orderly.
* Assists patients in the use of toilet facilities, including bedpans.
* Assists patients with ambulation, including the use of walkers and wheelchairs, when applicable.
* Assists patients with feeding, when needed.
* Assists patient with fluid intake, as directed, and measures and records fluid intake and output.
* Repositions patient, as appropriate.
* Checks diapers/under pads with each position change and ensures patient cleanliness; provides linen change as needed.
* Utilizes proper patient identification system, i.e. two patient identifiers.
Minimum Education:
* High school diploma or equivalent required.
Required Skills:
* Requires critical thinking skills, decisive judgment, and the ability to work with minimal supervision.
* Must be able to work in a stressful environment and take appropriate action.
* Requires ability to read and write legibly and carry out directions promptly and accurately.
* Must exhibit effective communication skills and interpersonal skills.
* Must be able to demonstrate the knowledge and skills necessary to provide care appropriate to the age of the patients served.
* Requires the ability to respond quickly and calmly under stressful or emergencies.
* Requires flexibility in scheduling and ability to work all shift patterns including weekends and holidays to ensure continuity of care and appropriateness of nursing coverage to the patients of Sovah Health Danville on all units.
Required Certifications/Licenses:
* AHA Basic Life Support (BLS) required.
Minimum Work Experience:
* One (1) year as a CNA, Respiratory Care Assistant, Rehab Tech, Certified Medical Assistant, EKG Tech, EMT, Phlebotomist, or equivalent clinical experience preferred.
EEOC Statement:
SOVAH Health - Martinsville is committed to providing Equal Employment Opportunities for all applicants and employees and complies with all applicable laws prohibiting discrimination against any employee or applicant for employment because of color, race, sex, age, religion, national origin, disability, genetic information, gender identity, sexual orientation, veterans' status or any other basis protected by applicable federal, state or local law.
Equal opportunity and affirmative action employers and are looking for diversity in candidates for employment: Minority/Female/Disabled/Protected Veteran
Clinical Research Coordinator
Clinical Research Coordinator Job 10 miles from Kernersville
PETERS MEDICAL RESEARCH "Partnering with patients today for tomorrow's miracles!" "Established Clinical Research Company is seeking a Clinical Research Study Coordinator to join our team in High Point!" Job Description * Complete QC of patient medical records and source documentation.
►Assist in managing all regulatory documents
►Assist with managing clinical trials, collecting data, informing participants about study objectives, and administering questionnaires.
* Act as a point of contact for sponsors/CROs. Facilitate and coordinate monitoring visits.
* Support marketing activities, as needed.
* Maintain clinical research professional credentials.
Requirements
* Employee must be available during "core" clinic hours of 8:00 a.m. to 5:00 p.m., Monday through Friday with some flexibility to work from 1-3 hours on Saturday, if needed.
* This is not a remote position as it requires direct patient care in a clinical setting.
* 2+ years of Clinical Research experience is required
* Bachelor's Degree is required
* Phlebotomy certification is required
Skills
* Ability to collect patient vitals and ECGs. A medical degree is not required. CNA or CMA certification preferred.
* Knowledge of GCP and applicable government FDA regulations. Current GCP Certification preferred.
* Strong team player and quick to help resolve problems.
* Knowledgeable of medical and research terminology, laboratory sanitation, and safety guidelines.
* Friendly with patients and clinic staff. Great communication skills, including verbal, written, and personal.
* Proficient in MS Applications. Solid data entry skills. EMR and EDC database experience preferred.
* Extremely detail-oriented with a focus on quality. Capable of multi-tasking in a fast-paced clinic environment.
* Reliable and dependable to finish projects, deliverables, and tasks on time without close supervision.
* Outstanding organizational skills in managing paper and electronic documents.
Competitive Benefit Package Includes:
* Competitive Yearly Compensation (Compensation commensurate with experience)
* Medical/Dental/Vision
* Generous PTO
* Company Paid Holidays
* Company matched 401K Plan
* And more!
Peters Medical Research is affiliated with Bethany Medical:
Bethany Medical is the largest independent established multi-specialty group in Central North Carolina, serving the Triad and surrounding communities for over 35 years. Bethany Medical is open 7 days a week, with 13 convenient locations and 16 practices in Greensboro, Winston-Salem, High Point, Kernersville, Jamestown, North Wilkesboro, and Mt Airy, North Carolina. We have grown to provide the facilities, staff, and support to offer urgent care, primary care, diagnostic testing, outpatient ancillary, and specialty care services on-site. Bethany Medical is staffed with board-certified physicians and providers representing 16 medical specialties. Practice staff members are known for treating each patient with prompt personalized care and attention. Bethany Medical employs over 65 providers and over 550 employees.
About the Triad:
The Triad area includes Greensboro (3rd Largest City in NC), Winston Salem, High Point, and the surrounding area. The Triad is centrally located in NC with a population of 1.9 million. The Triad is 1 hour from the mountains and 3 hours from the beach. Charlotte and Raleigh are 1.5 hours from the Triad. The Triad offers all the amenities of a larger city without all the traffic. The Piedmont Triad International Airport is conveniently located in Greensboro with convenient non-stop flights to most major cities. Enjoy an outstanding quality of life with no shortage of arts, entertainment, recreation, shopping, and hundreds of restaurants. The Triad is home to 85 colleges and universities including Wake Forest University, High Point University, UNC-Greensboro, NC A&T, Guilford College, Bennett College, and Greensboro College.
#IND100