Clinical Research Coordinator at Community Health Network

Cumnock, Scotland, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

25 Dec, 25

Salary

0.0

Posted On

26 Sep, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Data Management, Phlebotomy, ECG Testing, Informed Consent, Problem Solving, Communication, Safety Compliance, Budgeting, Patient Education, Team Collaboration, Protocol Adherence, Laboratory Specimen Processing, Data Collection, Eligibility Screening, Meeting Attendance

Industry

Hospitals and Health Care

Description

Join Community Community Health Network has an excellent opportunity available within our clinical research department. If you are looking for challenging work and meaningful advancement, then you should consider a career with Community. Make a Difference The Clinical Research Coordinator will be responsible for assessing, planning, implementing, and executing clinical research protocols in conjunction with the Principal Investigator and clinical research team Your Exceptional Qualifications Research Coordinator Duties: Identifies and screens appropriate candidates for eligibility for research studies. Obtains informed consent from eligible patients for a research study. Maintains an effective data management system to track study participants and activities. Collects data and completes case report forms and data queries as specified by the study protocol. Prepares source documents for data collection. Assists in identifying study related procedures for the project budget. · Administrative Duties: Attends Investigator and Coordinator Meetings as requested by the sponsor along with appropriate department, division and/or service line meetings. Assists in determining facility, staff and supply needs required for set-up and implementation of a new study. Prepares for and is present for sponsor representative site visits. Serves as an educator and resource person for patients, family, staff and physicians. · Laboratory Duties: Performs phlebotomy, ECG and other testing, as needed after trained. Prepares and processes laboratory specimens for shipment according to study lab manual. Reviews labs and ancillary tests; and reports results to Principal Investigator and appropriate personnel in timely manner. · Interpersonal Skills: Effectively problem solves and informs Manager and Principal Investigator when appropriate. · Communication: Communicates on a regular basis with the Investigators, Research Team, Hospital Staff, Monitor and other sponsor representatives to ensure adherence to Good Clinical Practice (GCP) guidelines. · Safety & Compliance: Coordinates, implements and completes clinical research studies in accordance with protocol guidelines, GCP, ICH, local, state and federal standards. Monitors adherence to protocols, and reports violations in a timely manner to the sponsor and the IRB. · Individuals may not perform all of these duties, or may perform additional, related duties not listed here. EDUCATION 2 year / Associate Degree (Required) 4 year / Bachelor's Degree (Preferred) In lieu of the above education requirements, a combination of experience and education will be considered. LICENSE & CERTIFICATION REQUIREMENTS within three (3) years from hire Certifications/Licensures: (Certified Clinical Research Associate (CCRA - ACRP), Certified Clinical Research Coordinator (CCRC-ACRP), Certified Clinical Research Professional (CCRP-SoCRA)) EXPERIENCE Previous experience in data abstraction is helpful (Preferred) Minimum of 2 years in a related field of healthcare (Required)

Responsibilities

The Clinical Research Coordinator will assess, plan, implement, and execute clinical research protocols in conjunction with the Principal Investigator and clinical research team. Responsibilities include identifying and screening candidates, obtaining informed consent, and maintaining data management systems.