Top 96 Market research Jobs in Charleston, Wv

Clinical Research Coordinator (Onsite)
US Foot & Ankle Specialists —Charleston, WV
- Mid-level
- Team management
- Organizational skills
- Paid holidays
- Disability insurance
Quick Apply
Patient Educator
TSP (A Syneos Health Company) —Charleston, WV
- $185,000 - $190,000 a year
- Bilingual
- Up to 50% travel
- HIPAA
- Paid parental leave
- Health savings account
HRIS Time Administrator - REMOTE
Ryder System —Charleston, WV
- Full-time
- Remote
- Microsoft Outlook
- Data analysis skills
- Mid-level
- Disability insurance
- Health insurance
Administrative Services Manager 1
State of West Virginia —Kanawha County, WV
- $43,357 - $75,789 a year
- Full-time
- Office
- Master's degree
- Administrative experience
13d
MARKETING SPECIALIST - AG EVENTS and AGRITOURISM (Guthrie Agricultural Center, Guthrie, WV)
WV Department of Agriculture —Charleston, WV
- $41,000 - $46,000 a year
- Marketing
- Public speaking
- Mid-level
Marketing Manager
Trulieve —South Charleston, WV
- Weekends as needed
- Remote
- Background check
- Microsoft Excel
- Marketing
- Paid time off
Quick Apply
Clinical Research Coordinator -- CLINICAL TRIALS CENTER -- Memorial-MSOB
CAMC Health System —Charleston, WV
- Overtime
- Customer service
- Mid-level
- Master's degree
Sr. Transaction Coordinator - Remote or Hybrid
Cushman & Wakefield —Charleston, WV
- $55,250 - $65,000 a year
- Full-time
- Remote
- Mid-level
- 2 years
- Health savings account
- Disability insurance
Quick Apply
11d
SCM Accounts Analyst
MRC Global —Charleston, WV
- Full-time
- Microsoft Outlook
- Up to 50% travel
- 5 years
Clinical Research Coordinator -- CLINICAL TRIALS CENTER -- Memorial-MSOB
Mon Health —Charleston, WV
- Overtime
- Customer service
- Mid-level
- Master's degree
Client Intake Manager
FBT Gibbons LLP —Charleston, WV
- Full-time
- Remote
- Microsoft Outlook
- 3 years
- Bachelor's degree
- Profit sharing
- Paid parental leave
Senior Financial Analyst - REMOTE
Ryder System —Charleston, WV
- $85,000 - $92,000 a year
- Full-time
- Remote
- Microsoft Word
- Microsoft Access
- Mid-level
- Disability insurance
- Health insurance
4d
Product Owner, FMS/Financial Intermediary Svc
Benelynk —Charleston, WV
- $120,000 - $125,000 a year
- Full-time
- Remote
- Pass drug screening
- Analysis skills
- Continuous improvement
- Health insurance
- Dental insurance
ASSISTANT DIRECTOR, PLANT INDUSTRIES DIVISION (Guthrie Agricultural Center, Guthrie, WV)
WV Department of Agriculture —Charleston, WV
- $60,000 - $65,000 a year
- Writing skills
- Research
- Ability to lift 50 pounds
Marketing Specialist
YWCA Charleston —Charleston, WV
- $40,000 - $45,000 a year
- Full-time
- Marketing
- Mid-level
- Driver's License
Quick Apply
2d
Transportation Purchasing Specialist - Kanawha County
West Virginia Department of Transportation —Charleston, WV
- $38,494.14 - $54,244.11 a year
- Full-time
- Writing skills
- Mid-level
- Office
- Paid holidays
- Disability insurance
4d
Business Development Manager
CDI Engineering Services —Charleston, WV
- Online Application
- Remote
- Research
- US work authorization
- Contracts
5d
Science & Medicine Advisor
American Heart Association —Charleston, WV
- $110,000 - $120,000 a year
- Full-time
- Medicine
- Office
- Doctor of Philosophy
- Wellness program
- Paid holidays
Real Estate Specialist 1
State of West Virginia —Kanawha County, WV
- $39,461 - $68,582 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
Sales Representative (Charleston, WV)
Sysco —Charleston, WV
- $44,200 - $73,600 a year
- Weekends as needed
- Marketing
- Computer literacy
- Restaurant management
- Mileage reimbursement
- Employee stock purchase plan

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Clinical Research Coordinator (Onsite)

US Foot & Ankle Specialists -
Charleston, WV

Quick Apply

Job Details

Benefits

Paid holidays
Disability insurance
Health insurance
Paid time off
401(k) matching
Employee discount
Life insurance

Qualifications

Medical terminology

Full Job Description

This is an on-site role. Candidates must be local to Charleston, WV.

We are seeking an experienced Clinical Research Coordinator (CRC) to independently manage and execute clinical trials at the site level. This role is responsible for overseeing day-to-day study operations, regulatory compliance, patient coordination, and data management in accordance with protocol, GCP guidelines, and internal SOPs.

Job Purpose:

Coordinate research and administrative procedures for the successful management of clinical trials
Ensure SOPs are followed
Perform diverse administrative duties pertaining to clinical research
Manage trial operations

Essential Functions/Responsibilities (other duties may be assigned):

Monitors study activities to ensure compliance with protocols and with relevant local, federal, and state regulatory, institutional policies, and FASMA SOPs.
Has an in-depth knowledge of protocol requirements.
Acts as liaison between the investigators, medical providers, the Institutional Review Board (IRB), CRO and sponsor.
Maintains required records of study activity including Case Report Forms (CRFs), source, narrative notes, drug dispensing records, and all regulatory forms.
Tracks enrollment status of subjects and documents withdrawal information such as withdrawal causes and subject contact efforts.
Inputs and uploads subject information and pertinent clinical data to study specific study databases and/or EDC (Electronic Data Capture) sites and FASMA Clinical Trial Management System (CTMS) within appropriate timeframe defined by the protocol, sponsor, and SOPs.
Assesses eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians, nurses, medical assistants, and other staff. Enters potential subject demographics into FASMA CTMS.
Oversees subject enrollment to ensure that informed consent is properly obtained and documented.
Records adverse event and side effect data and confers with investigators regarding the reporting of events to oversight agencies.
Records and reports serious adverse events to the sponsor or other regulatory authorities within the appropriate reporting guidelines and timeframe.
Prepares, participates, and documents quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
Identifies protocol problems, informs investigators of problems, and assists in problem resolution efforts such as protocol revisions.
Manages the inventory of equipment and supplies related to each study. This includes ordering of Investigational Product (IP), temperature recording devices, calibrations, and all necessary supplies for study completion.
Prepares study-related documentation such as protocol worksheets, source, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
Maintains complete regulatory files and Investigator Site File (ISF). This includes completing all appropriate subject logs, screening and enrollment logs, study product/IP accountability logs, training documents, filing all applicable documents, correspondence etc.
Completes and submits IRB initial, renewal and closure applications.
Instructs research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, and documentation procedures.
Collaborates with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions. Communicates with laboratories or investigators regarding laboratory findings.
May assist with contracting with local vendors such as local laboratory.
Reviews scientific literature and participates in relevant education activities to maintain knowledge of clinical studies affairs and issues.
Maintains Good Clinical Practice (GCP) certification and all other project specific certifications.
Maintains accurate and legible records, following ALCOA (Attributable, Legible, Contemporaneous, Original and Accurate) principles
Manages site specific research staff CV’s, licenses and applicable trainings (i.e. GCP, IATA, etc.)
Ensures site has all appropriate credentials and certifications (i.e. IATA, CLIA, etc.). If applicable, with approval, assist with renewal or apply for appropriate credentials and certifications.
Acts as a contact liaison for study participants by answering questions and keeping them informed of study protocol.
Communicates with manager with all pertinent study related progress, issues and when subjects have completed the trial.
Arranges for secure retention of all study documents in accordance with sponsor requirements and site SOP, whichever is longer.
Manage all locked areas where investigational or study products and supplies are stored.
Tracks and maintains temperature and maintenance logs and/or devices for research related equipment.
Draws blood or supervises the on-site drawing of blood as dictated by the research protocol. For delegated blood draws, document fully on the Delegation of Authority log. Coordinates local lab draws as needed. For post markets studies, this will usually only involve a finger stick. Acquires other lab requirements as necessary per protocol.
Manages the day-to-day activities of each study including trial operations, problem solving, communication, inventory control, and protocol management.
Maintain strict confidentiality and blinding protocol, if applicable, at all times.
Responds to study queries within appropriate timeframe defined by the protocol, sponsor, and SOPs.

Required Skills and Experience:

Preferable to have an Associate’s degree in business administration, biology, health sciences, healthcare or any related field, or comparable clinical research industry experience.
Preferable to have a minimum of 2 years of Site Coordinating experience. Must have exceptional technical and communication skills. Candidate needs the ability to be proactive, multitask and maintain excellent organizational skills.
Excellent attention to detail
Knowledge of biological and medical terminology
Understanding of the principles of administration and management
Superior organizational and time management
Capable of working independently and also as part of a team
Excellent verbal and written communication skills
Superior multi-tasking skills

Benefits Offered:

Health Insurance (Single & Family plans available)
Life Insurance
Disability Insurance
401(k) Plan with Company Match
Employee Discount Program
Paid Time Off
Paid Holidays

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

Quick Apply

Refine Your Search

market research jobs in charleston, wv

Clinical Research Coordinator (Onsite)

Patient Educator

HRIS Time Administrator - REMOTE

Administrative Services Manager 1

MARKETING SPECIALIST - AG EVENTS and AGRITOURISM (Guthrie Agricultural Center, Guthrie, WV)

Marketing Manager

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

Sr. Transaction Coordinator - Remote or Hybrid

SCM Accounts Analyst

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

Client Intake Manager

Senior Financial Analyst - REMOTE

Product Owner, FMS/Financial Intermediary Svc

ASSISTANT DIRECTOR, PLANT INDUSTRIES DIVISION (Guthrie Agricultural Center, Guthrie, WV)

Marketing Specialist

Transportation Purchasing Specialist - Kanawha County

Business Development Manager

Science & Medicine Advisor

Real Estate Specialist 1

Sales Representative (Charleston, WV)

I want to receive the latest job alert for market research in charleston, wv

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