Top 16 Clinical research coordinator Jobs in Charleston Wv

Research Assistant I -- Clinical Trials Center -- Memorial-MSOB
CAMC Health System —Charleston, WV
- Overtime
- Customer service
- Business development
- Associate's degree
6d
Research Assistant I -- Clinical Trials Center -- Memorial-MSOB
Mon Health —Charleston, WV
- Overtime
- Customer service
- Business development
- Associate's degree
11d
Clinical Research Coordinator (Onsite)
US Foot & Ankle Specialists —Charleston, WV
- Mid-level
- Team management
- Organizational skills
- Paid holidays
- Disability insurance
Quick Apply
Clinical Research Coordinator -- CLINICAL TRIALS CENTER -- Memorial-MSOB
CAMC Health System —Charleston, WV
- Overtime
- Customer service
- Mid-level
- Master's degree
Clinical Research Coordinator -- CLINICAL TRIALS CENTER -- Memorial-MSOB
Mon Health —Charleston, WV
- Overtime
- Customer service
- Mid-level
- Master's degree
Clinical Coordinator Radiologic Technology Program
University of Charleston —Charleston, WV
- Full-time
- Clinic experience
- Mid-level
- Ability to lift 50 pounds
Clinical Management Coordinator -- GMICU -- General Hospital
Mon Health —Charleston, WV
- Overtime
- Nursing
- RN License
- Hospital
11d
Clinical Management Coordinator -- Emergency Department -- Memorial Hospital
Mon Health —Charleston, WV
- Overtime
- Nursing
- RN License
- Customer service
Clinical Management Coordinator
Charleston Area Medical Center (CAMC) —Charleston, WV
- Overtime
- Doctoral degree
- Customer service
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Coordinator - Critical Care
THOM Thomas Hospitals —South Charleston, WV
- Full-time
- Nursing
- Patient monitoring
- RN License
1d
Clinical Management Coordinator -- ICU Medical -- Memorial Hospital
CAMC Health System —Charleston, WV
- Overtime
- Nursing
- RN License
- Customer service
Clinical Management Coordinator -- GMICU -- General Hospital
CAMC Health System —Charleston, WV
- Overtime
- Nursing
- RN License
- Hospital
6d
Clinical Management Coordinator -- ICU Medical -- Memorial Hospital
Mon Health —Charleston, WV
- Overtime
- Nursing
- RN License
- Customer service
Clinical Management Coordinator -- Emergency Department -- Memorial Hospital
CAMC Health System —Charleston, WV
- Overtime
- Nursing
- RN License
- Customer service
Manager Clinical Research
U.S. Renal Care —United States
- $94,920 - $142,380 a year
- Full-time
- Senior level
5d

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Clinical Research Coordinator (Onsite)
US Foot & Ankle Specialists —Charleston, WV
Preferable to have an Associate’s degree in business administration, biology, health sciences, healthcare or any related field, or comparable clinical research…
Quick Apply
MICROBIOLOGIST I (Guthrie Agricultural Center, Guthrie, WV)
WV Department of Agriculture —Charleston, WV
Valid driver's license is required. Substantial knowledge of the source materials found in the field of bacteriology and chemistry. Write SOPs and test methods.
$42,000 - $46,000 a year

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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…
Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…

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Research Assistant I -- Clinical Trials Center -- Memorial-MSOB

CAMC Health System -
Charleston, WV

Apply Now

Job Details

Full-time
6 days ago

Qualifications

Statistics
Laboratory project records management
Data analysis reporting
Informed consent
Project documentation
Data validation techniques
Customer service
Data preparation projects
Filing
Scanning
Data summary reports
Research project coordination
Business development
Records management
Grant proposals
Informed consent procedures implementation
Medical record abstraction
Research compliance clinical trial records management
Implementing research protocols
Patient recruitment
Communication with regulatory authorities for clinical trials
Literature search services
Patient interaction
Journal articles
Continuous quality improvement (CQI)
Research participation
Document change management
Associate's degree
Ethical review application preparation
Research findings presentation

Full Job Description

Job Summary

To provide support to the Director of the Center, or Principal Investigator/Study Coordinator in all appropriate functions related to the conduct of a research investigation.

Responsibilities

Administrative/Regulatory 50%

Primarily provide support to the research team, comprising the research director, investigator

and/or study coordinator

Process and organize new protocols and assist in preparing IRB and grants documentation for

institutional approval, including revisions, addendums, renewals and signatures/approval as
directed.

Document that IRB has been notified of a protocol change that is administrative or significant;

confirm all IRB approvals.

Assist researchers in preparing documents for institutional grants and research office and for IRB.
Maintain accurate filing specific to each study and be able to track original and subsequent activity

as well as approval documentation.

Research Study Management 35%

Assist with informed consent and subject/patient enrollment
Process and organize new research-related information and data.
Collect data from the medical record, populating research data collection forms
Collect and manage data needed per study. Includes creating surveys, scanning surveys, cleaning

data, analyzing data, generating reports, and creating graphs or tables.

Maintain and organize all required records, data, reports, and statistics per study.
Assist in the preparation of grant applications and editing of articles and manuscripts.
Search scientific journals for information.
Verify and check data.

Physician and Patient Communication 10%

Communicate findings/results to interested groups, Project Director and/or Principal Investigator.
Under the direction of the PI and/or the research coordinator, may communicate with

patient/subject and/or subject’s family.

Teamwork/Development 3%

Serve as an ancillary research team member integral to trial success
Participate in departmental and study meetings as directed

Business Development 2%

Depict a professional image and competence in relation to our sponsors and investigators with a

goal of increasing the likelihood of repeat business.

Knowledge, Skills & Abilities

Patient Group Knowledge (Only applies to positions with direct patient contact)

The employee must possess/obtain (by the end of the orientation period) and demonstrate the knowledge and skills necessary to provide developmentally appropriate assessment, treatment or care as defined by the department’s identified patient ages. Specifically the employee must be able to demonstrate competency in: 1) ability to obtain and interpret information in terms of patient needs; 2) knowledge of growth and development; and 3) understanding of the range of treatment needed by the patients.

Competency Statement

Must demonstrate competency through an initial orientation and ongoing competency validation to independently perform tasks and additional duties as specified in the job description and the unit/department specific competency checklist.

Common Duties and Responsibilities
(Essential duties common to all positions)

1. Maintain and document all applicable required education.
2. Demonstrate positive customer service and co-worker relations.
3. Comply with the company's attendance policy.
4. Participate in the continuous, quality improvement activities of the department and institution.
5. Perform work in a cost effective manner.
6. Perform work in accordance with all departmental pay practices and scheduling policies, including but not limited to, overtime, various shift work, and on-call situations.
7. Perform work in alignment with the overall mission and strategic plan of the organization.
8. Follow organizational and departmental policies and procedures, as applicable.
9. Perform related duties as assigned.

Education

Bachelor's Degree (Required)

Experience: Bachelor's Degree and strong interest in research or medical research-related field

Substitution: Associate degree may substitute for Bachelor’s degree if related experience

Credentials

Work Schedule: Days

Status: Full Time Regular 1.0

Location: Memorial-MSOB

Location of Job: US:WV:Charleston

Talent Acquisition Specialist: Tamara B. Young [email protected]

Apply Now

Refine Your Search

clinical research coordinator jobs in charleston wv

Research Assistant I -- Clinical Trials Center -- Memorial-MSOB

Research Assistant I -- Clinical Trials Center -- Memorial-MSOB

Clinical Research Coordinator (Onsite)

Clinical Research Coordinator -- CLINICAL TRIALS CENTER -- Memorial-MSOB

Clinical Research Coordinator -- CLINICAL TRIALS CENTER -- Memorial-MSOB

Clinical Coordinator Radiologic Technology Program

Clinical Management Coordinator -- GMICU -- General Hospital

Clinical Management Coordinator -- Emergency Department -- Memorial Hospital

Clinical Management Coordinator

Clinical Coordinator - Critical Care

Clinical Management Coordinator -- ICU Medical -- Memorial Hospital

Clinical Management Coordinator -- GMICU -- General Hospital

Clinical Management Coordinator -- ICU Medical -- Memorial Hospital

Clinical Management Coordinator -- Emergency Department -- Memorial Hospital

Manager Clinical Research

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