Clinical Research Associate IIIIII

Type of Position:

Job Type:

Institution Name:

The University of Arkansas for Medical Sciences (UAMS) has a unique combination of education research and clinical programs that encourages and supports teamwork and diversity. We champion being a collaborative health care organization focused on improving patient care and the lives of Arkansans.

UAMS offers amazing benefits and perks available for benefits eligible positions only:

• Health: Medical Dental and Vision plans available for qualifying staff and family
• Holiday Vacation and Sick Leave
• Education discount for staff and dependents (undergraduate only)
• Retirement: Up to 10 matched contribution from UAMS
• Basic Life Insurance up to $50000
• Career Training and Educational Opportunities
• Merchant Discounts
• Concierge prescription delivery on the main campus when using UAMS pharmacy

Below you will find the details for the position including any supplementary documentation and questions you should review before applying for the opening. To apply for the position please click theApply link/button.

Persons must have proof of legal authority to work in the United States on the first day of employment.

All application information is subject to public disclosure under the Arkansas Freedom of Information Act.

Departments Website:

Summary of Job Duties:

Qualifications:

Level I

• Bachelors degree plus three 3 years of researchrelated experience required.

• Obtain Certified Research Specialist (CRS) certification within 2 years of hire.

Level II

• Bachelors degree plus three 3 years of researchrelated experience with demonstrated proficiency in a functional area required.

• Obtain CRS certification within 2 years of hire.

Level III

• Bachelors degree plus five 5 years of researchrelated experience with demonstrated proficiency in a functional area required.

• Certified Clinical Research Professional (CCPR) Certified Clinical Research Associate (CCRA) or equivalent professional certification.

Knowledge Skills & Abilities:

• Must have excellent computer skills.

• Ability to use the Microsoft Office suite at a high level of proficiency is essential.

• Excellent written and verbal communication skills.

• Ability to work collaboratively and sensitively with incarcerated individuals and with community partners.

• Must be able to drive for instate travel.

• Proficiency with online survey software (REDCap Qualtrics) preferred.

• Knowledge of human subjects behavioral research preferred.

• Experience conducting research with vulnerable populations in the area of traumatic stress i.e. incarcerated persons people with PTSD) preferred.

Additional Information:

Responsibilities:

• Manages research team schedules.

• Maintains calendar and provides scheduling assistance for the Principal Investigator and project teams.

• Schedules grantrelated meetings (e.g. speaker series research meetings study/project participant assessment sessions).

• Works with internal and external partners to facilitate project activities including working with department administration to acquire needed equipment/programs.

• Assists with participant assessment scheduling and retention efforts and with informing the broader research team of study activities to promote coordination across projects.

• Sets meeting agendas takes notes and distributes aftermeeting action items.

• Engages with organizations and agencies to accomplish research objectives.

• Develops tools to track research team metrics and reports. Updates tracking tools regularly.

• Bears primary responsibility for ensuring that laboratory space is clean and organized. Monitors and manages laboratory supplies.

• May oversee other staff and/or student trainees in executing project activities including data collection.

• Performs initial contact with prospective research subjects.

• Monitors the information for eligibility for the specific protocol as well as accuracy and completeness prior to examination by the investigators and/or sponsoring agency.

• Collects codes and enters study information into a database.

• Assists in data compilation.

• Maintains records and study information and prepares reports and summaries as needed.

• Ensures that completed questionnaires are complete legible and accurate in accordance with research protocols.

• Makes followup contact with participants to obtain missing or questionable data.

• Maintains complete & accurate records and files pertaining to one or more research studies.

• Maintains detailed records of research subject visits and procedures.

• Transcribes qualitative data and prepares for upload to qualitative analysis software.

• Conducts qualitative coding.

• Makes descriptive reports of research study progress and outcomes.

• Builds instructions for scoring research assessments.

• May conduct more advanced analyses under the direction of the PI.

• Assists in the preparation and submission of grant proposals grant reports manuscripts and lay reports.

• Reviews literature for related research developments & compiles findings

• Performs other duties as assigned.

Salary Information:

Required Documents to Apply:

Special Instructions to Applicants: