DescriptionMarket Range: 10
Hiring Salary: $4182.12 - $5416.67/Monthly
THIS IS A GRANT FUNDED POSITION AND WILL RENEW ANNUALLY PENDING FUNDING AVAILABLITY
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: Under the direction of the medical director and director of research the Clinical Coordinator promotes good clinical practices on behalf of plastic surgery clinical trials by possessing in-depth knowledge of federal regulations.
ResponsibilitiesDUTIES AND RESPONSIBILITIES:
- Assists with ensuring all ongoing or anticipated clinical studies and related activities are performed according to federal regulations as well as university and sponsoring agency policies and procedures.
- Reviews and develops a familiarity with the study protocols (i.e. study proceedings and timelines inclusion and exclusion of criteria confidentiality etc.).
- Assists the medical director with communicating study requirements to all individuals involved.
- Screens subjects for eligibility.
- Prepares study material as requested.
- Maintains regulatory documents prepares protocols handles consent forms for submission to the UT IRB Office for initial and ongoing reviews.
- Ensures study participants are safe and fully informed.
- Performs clinical workups and follow-ups with patients as indicated by study protocols.
- Serves as clinical liaison between clinical studies and others involved in projects including patients physicians nurses data collectors and evaluators.
- Maintains documents related to clinical trials and human participant protection.
- Ensures compliance with protocol and regulatory requirements manages patient protocol activities assures patient safety collects records and maintains data and source documentation.
- Assists the residents and fellows in the collection of data and manuscript preparation.
- Performs other related duties as assigned.
QualificationsMINIMUM REQUIREMENTS:
EDUCATION:Registered Nurse. (TRANSCRIPT REQUIRED)
EXPERIENCE: Two (2) years of nursing or medical care in a clinical setting in which one (1) is within a research environment; OR Masters Degree in lieu of experience; OR a combination of college course work and work experience to equal six (6) years.
LICENSES:R.N. or B.S.N. Current TN Registered Nurse License required.
KNOWLEDGE SKILLS AND ABILITIES:
- Thorough understanding and knowledge of the research process and terminology.
- Knowledge of the specialty under investigation.
- Management and organizational skills.
- Instructing monitoring data management and critical thinking skills.
WORK SCHEDULE: This position may occasionally be required to work evenings and weekends.
Required Experience:
IC
DescriptionMarket Range: 10Hiring Salary: $4182.12 - $5416.67/MonthlyTHIS IS A GRANT FUNDED POSITION AND WILL RENEW ANNUALLY PENDING FUNDING AVAILABLITYJOB SUMMARY/ESSENTIAL JOB FUNCTIONS: Under the direction of the medical director and director of research the Clinical Coordinator promotes good cli...
DescriptionMarket Range: 10
Hiring Salary: $4182.12 - $5416.67/Monthly
THIS IS A GRANT FUNDED POSITION AND WILL RENEW ANNUALLY PENDING FUNDING AVAILABLITY
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: Under the direction of the medical director and director of research the Clinical Coordinator promotes good clinical practices on behalf of plastic surgery clinical trials by possessing in-depth knowledge of federal regulations.
ResponsibilitiesDUTIES AND RESPONSIBILITIES:
- Assists with ensuring all ongoing or anticipated clinical studies and related activities are performed according to federal regulations as well as university and sponsoring agency policies and procedures.
- Reviews and develops a familiarity with the study protocols (i.e. study proceedings and timelines inclusion and exclusion of criteria confidentiality etc.).
- Assists the medical director with communicating study requirements to all individuals involved.
- Screens subjects for eligibility.
- Prepares study material as requested.
- Maintains regulatory documents prepares protocols handles consent forms for submission to the UT IRB Office for initial and ongoing reviews.
- Ensures study participants are safe and fully informed.
- Performs clinical workups and follow-ups with patients as indicated by study protocols.
- Serves as clinical liaison between clinical studies and others involved in projects including patients physicians nurses data collectors and evaluators.
- Maintains documents related to clinical trials and human participant protection.
- Ensures compliance with protocol and regulatory requirements manages patient protocol activities assures patient safety collects records and maintains data and source documentation.
- Assists the residents and fellows in the collection of data and manuscript preparation.
- Performs other related duties as assigned.
QualificationsMINIMUM REQUIREMENTS:
EDUCATION:Registered Nurse. (TRANSCRIPT REQUIRED)
EXPERIENCE: Two (2) years of nursing or medical care in a clinical setting in which one (1) is within a research environment; OR Masters Degree in lieu of experience; OR a combination of college course work and work experience to equal six (6) years.
LICENSES:R.N. or B.S.N. Current TN Registered Nurse License required.
KNOWLEDGE SKILLS AND ABILITIES:
- Thorough understanding and knowledge of the research process and terminology.
- Knowledge of the specialty under investigation.
- Management and organizational skills.
- Instructing monitoring data management and critical thinking skills.
WORK SCHEDULE: This position may occasionally be required to work evenings and weekends.
Required Experience:
IC
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