Hello,

Thank you for your interest in career opportunities with the University of Mississippi Medical Center.  Please review the following instructions prior to submitting your job application:

• Provide all of your employment history, education, and licenses/certifications/registrations.  You will be unable to modify your application after you have submitted it.
• You must meet all of the job requirements at the time of submitting the application. 
• You can only apply one time to a job requisition. 
• Once you start the application process you cannot save your work. Please ensure you have all required attachment(s) available to complete your application before you begin the process.
• Applications must be submitted prior to the close of the recruitment. Once recruitment has closed, applications will no longer be accepted.

After you apply, we will review your qualifications and contact you if your application is among the most highly qualified. Due to the large volume of applications, we are unable to individually respond to all applicants. You may check the status of your application via your Candidate Profile.

Thank you,

Human Resources

Important Applications Instructions:

Please complete this application in entirety by providing all of your work experience, education and certifications/

license.  You will be unable to edit/add/change your application once it is submitted.

Job Requisition ID:

R00039265

Job Category:

Research

Organization:

SOM-Orthopedic Surgery-DBA

Location/s:

Main Campus Jackson

Job Title:

Manager-Clinical Research - SOM-Orthopedic Surgery

Job Summary:

Responsible for the coordination, management, and day-to-day execution of all clinical trials and research projects conducted in the clinical research program. Responsibilities include supervision of personnel; documentation,
Standardization, and evaluation of clinical procedures and protocols; and coordination of compliance activities.

Education & Experience

Master's degree in Nursing, Public Health, or related field plus three (3) years of research experience or equivalent combination of education/experience.

Certifications, Licenses or Registration Required:  Certified Clinical Research Coord (CCRC) preferred

Knowledge, Skills & Abilities

Excellent knowledge of good clinical practice FDA, OSHA, and quality assurance regulations.  Superior oral and written communication skills.  Ability to interact effectively with patients, physicians, staff, study sponsors, UMMC administrators, and federal regulators.  Strong knowledge of computer systems, tools and programs.  Self-motivated and self-directed; demonstrated ability to lead a clinical team.

Responsibilities

• Assumes responsibility for all aspects of study recruitment, enrollment, completion of all study visits for eligible participants.  Conducts operational clinic procedures and trains staff to conduct procedures according to study protocol, GCP, FDA and OSHA regulations.
• Establishes clinic goals and assesses progress toward goals; maximizes effective utilization of staff and resources.
• Assures confidentiality of study documents and oversees research participant follow-up and referrals.
• Monitors study budgets and billings to insure adequacy of funds and compliance with UMMC policies and federal regulations.
• Collaborates with investigators and directors to meet study objectives and resolve problems related to study budget, data, or activities.  Interacts with study sponsors, regulatory agencies, and UMMC compliance department on behalf of the study.
• Prepares standard operating procedures and policies for the study/program and oversees the implementation of those policies.  Oversees completion/submission of IRB documents, progress reports, and other study deliverables.
• 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 biohazardous 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 50%, constant-51% or more)

Time Type:

Full time

FLSA Designation/Job Exempt:

Yes

Pay Class:

Salary

FTE %:

100

Work Shift:

Day

Benefits Eligibility:

Benefits Eligible

Grant Funded:

Yes

Job Posting Date:

11/12/2024

Job Closing Date (open until filled if no date specified):