Research Study Coordinator 1-Preventive Medicine

Market Range: 08

Hiring Salary: $21.69/Hourly

THIS IS A GRANT-FUNDED POSITION FUNDED UNTIL JUNE 30 2027

JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Study Research Coordinator 1 conducts study visits with research participants as specified in the CANDLE study protocols. This position collaborates with the study staff to successfully achieve the goals of the study the principal investigator and the department in a timely manner.

DUTIES AND RESPONSIBILITIES:

1. Recruit participants for new study visits by explaining procedures and benefits of participating.
2. Facilitates informed consent/assent process in accordance with study protocols and Good Clinical Practice Guidelines while utilizing understanding of inclusion/exclusion criteria.
3. Completes study visits with participants as specified in the study protocol via face-to-face meetings telephone conversations and mailings.
4. Performs complex battery of cognitive and executive function testing with children using validated measures.
5. Assesses childrens health and development to ensure safety and eligibility for study procedures.
6. Performs pulmonary function tests using diagnostic testing software to assess lung function in children.
7. Completes an intensive sequence of sensitive data collection instruments via interview with child participants.
8. Performs preliminary assessment for child safety following responses to suicidal ideation questions.
9. Manages input storage and retrieval of biological samples for the CANDLE study.
10. Documents all adverse events medication adjustments and/or protocol deviations reported by study participants using protocol-specific forms and procedures while utilizing good clinical judgment.
11. Evaluates participant communication history to determine suitable contact method.
12. Serves as study participant primary contact.
13. Performs other duties assigned.

MINIMUM REQUIREMENTS:

EDUCATION:Bachelors Degree in Public Health Psychology Counseling Sociology or related social science field (TRANSCRIPT REQUIRED)

EXPERIENCE: One (1) year of clinical research experience; OR Masters Degree will be accepted in lieu of experience; ORa combination of education and experience to equal five (5) years.

LICENSE/CERTIFICATION: Must successfully obtain and renew certifications in all areas of the protocol good clinical practices and human subject compliance. Training is provided for all necessary certifications.(COPY OF LICENSE/CERTIFICATION REQUIRED)

KNOWLEDGE SKILLS AND ABILITIES:

• Excellent interpersonal organizational time-management and verbal and written communication skills.
• Ability to make good clinical judgment.
• Ability to function independently and as a member of a team.
• Ability to obtain Human Subject Protection and other applicable certifications within the first four weeks of employment.
• Computer skills including proficiency in using Microsoft Word and Excel and the ability to demonstrate proficiency in using Filmmaker within 3 months.
• Ability to communicate clearly and effectively with participants staff and faculty.

WORK SCHEDULE:This position may occasionally be required to work evenings and weekends.