Clinical Research Coordinator - PRN

ummc; Jackson (MS); On-site; USD 36,000 - 62,000; Part time

Job summary

University of Mississippi Medical Center in Jackson seeks a Clinical Research Coordinator - PRN to manage, execute, and report study results, supervise the research team, and coordinate activities for studies within the assigned unit. This role directs participant enrollment, ensures integrity of study records, and prepares IRB documents and progress reports.

Bachelor's degree in Health Sciences or related field with at least two years of clinical research experience is required; Master's degree

Qualifications

• Bachelor's Degree in a Health Sciences or related field with at least two years of Clinical Research experience.
• Master's Degree preferred.
• Certified Clinical Research Coordinator (CCRC) preferred.

Responsibilities

• Assumes responsibility for all aspects of study recruitment, screening, enrollment, and visits for eligible participants.
• Ensures staff are knowledgeable about study protocol and delineates roles.
• Oversees scheduling, documentation, and follow-ups with participants.

Skills

GCP and FDA regulations

Communication skills

Interpersonal skills

IRB submissions knowledge

Leadership in team environment

Education

Bachelor's degree in Health Sciences or related field

2+ years Clinical Research experience

Master's degree preferred

Job description

Job Requisition ID

R00053598

Job Category

Research

Organization

SOM-Peds-Neonatology-Mgr Research Operations

Location/s

Main Campus Jackson

Job Title

Clinical Research Coordinator - PRN

Job Summary

Responsible for management, execution, and reporting of clinical study results and the supervision of the research team. Coordinates activities for research studies within an assigned area or unit. Directs participant enrollment in research studies and assures integrity of study records. Prepares and submits documentation for institutional and governmental grant progress review and budget monitoring.

Education & Experience

Bachelor's Degree in a Health Sciences or related field and at least two (2) years of Clinical Research experience. Master's Degree preferred.

Certifications, Licenses or Registration Required

Certified Clinical Research Coordinator (CCRC) preferred.

Knowledge, Skills & Abilities

• Excellent knowledge of good clinical practice and FDA regulations.
• Superior oral and written communication skills.
• Strong interpersonal skills to effectively interact with patients, physicians, staff, and study sponsors.
• Knowledge and understanding of computer systems, tools, and programs.
• Ability to assume a leadership role in a team environment.
• Working knowledge of IRB submissions/amendments, patient screening and consenting.
• Excellent organizational skills.

Responsibilities

• Assumes responsibility for all aspects of study recruitment, screening, enrollment, and visits for eligible participants. Administers study-related procedures & instruments; directs participants for hospital and physician procedures.
• Ensures that research personnel are knowledgeable about all components of the study protocol and that staff roles and responsibilities are delineated.
• Oversees and manages scheduling, documentation, and follow-ups with research participants. Supervises patient education and referrals.
• Monitors study budgets and billings to insure adequacy of funds and compliance with UMMC policies and federal regulations.
• Corresponds with study investigators, sponsors, regulatory agencies, and UMMC compliance personnel on matters related to study documentation, records, data and operations.
• Prepares IRB documents and progress reports. Oversees maintenance of regulatory documents, files, and reports.
• The duties listed are general in nature and are examples of the duties and responsibilities performed and are not meant to be construed as exclusive or all-inclusive. Management retains the right to add or change duties at any time.

Physical and Environmental Demands

Requires frequent exposure to unpleasant or disagreeable physical environment such as high noise level and exposure to heat and cold, frequent handling or working with potentially dangerous equipment, frequent exposure to bio-hazardous conditions such as risk of radiation exposure, blood borne pathogens, fumes or airborne particles, and/or toxic or caustic chemicals which mandate attention to safety considerations, occasional working hours significantly beyond regularly scheduled hours, occasional travelling to offsite locations, occasional activities subject to significant volume changes of a seasonal/clinical nature, occasional work produced subject to precise measures of quantity and quality, frequent bending, occasional lifting and carrying up to 50 pounds, frequent crouching/stooping, occasional driving, occasional kneeling, frequent pushing/pulling, frequent reaching, frequent sitting, frequent standing, frequent twisting, and frequent walking. (occasional-up to 20%, frequent-from 21% to 5