Clinical Research Coordinator I - Psychiatry

Location
ST. LOUIS, MO 63108 Scheduled Hours
40

Position Summary
The Kids' Interactions, Thoughts, and Experiences (KITE) Project in Child & Adolescent Psychiatry at Washington University School of Medicine is seeking to hire a dedicated Clinical Research Coordinator I to join and amplify our growing research team. Our studies examine how social connection and disconnection influence the emergence of suicidal thoughts and behaviors (STBs) in young children. We investigate early developmental risk factors, characterize how STBs are expressed in childhood, and develop evidence-based approaches for screening and assessment in children ages 5-10. This is an exciting opportunity to be part of a team that is transforming the landscape of childhood mental health, and we offer a collegial and collaborative work culture that values your contributions.

In your role as a Clinical Research Coordinator I, you will bring your clinical research expertise to assist the Principal Investigator in a longitudinal study examining STBs and non-suicidal self-injury (NSSI) among children and preteens, involving clinical interviews and behavioral assessments. You may be responsible for several projects simultaneously, acting as a liaison with the sponsoring agency, community, and the study participants; responsible for managing and recording all phases of study protocol as required by sponsoring agency to ensure compliance. This position is primarily in-person, with the possibility of one remote day per week, depending on study needs. You will play an integral role in coordinating our research team, contacting and maintaining communication with research participants, and managing the day-to-day aspects of the study. We offer a collegial and collaborative work culture that values and respects your contributions. Close collaboration with our team of investigators and research staff will be central to your success in this position.

Primary Duties & Responsibilities:

• Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies.
• Establishes record-keeping systems; makes assessments and determinations of participants' progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify principal investigators with issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency and research sites.
• Contacts/enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews.
• Develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains research procedures to address participant/family concerns.
• Administers/scores assessments and/or evaluates all lab and clinical assessments to ensure they are completed in a valid manner.
• Ensures timely completion of all protocol requirements (assessment, EEG testing, procedures and payments) to include scheduling and facilitating the patient's completion of protocol requirements; evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same.
• Collects clinical and narrative interviews under clinical research protocols.
• Performs other duties incidental to the work described herein, as assigned by the PI, such as running EEG lab sessions, mailing payments, and interviewing research participants.
• Engage in thoughtful communication with principal investigators, other clinical team members, and research staff, fostering a spirit of teamwork in service of our research and clinical mission.
• Actively participate in continuous learning and professional development initiatives to stay at the forefront of research and clinical best practices.
• Uphold the highest standard of participant confidentiality, ensuring stringent adherence to HIPPA regulations and institutional research guidelines.
• Prepares/edits progress reports and attends meetings.
• May participate in training of Professional Rater I/II.
• Monitors and orders any supplies necessary for successfully conducting the research assessments.
• Performs other duties as assigned.

Working Conditions:
Job Location/Working Conditions

• Patient care setting.

Physical Effort

• Typically sitting at desk or table.

Equipment

• Office equipment.

The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time.

Required Qualifications

Education:
Bachelor's degree or combination of education and/or experience may substitute for minimum education.

Certifications /Professional Licenses :
The list below may include all acceptable certifications, professional licenses and issuers. More than one credential, certification or professional license may be required depending on the role.

Basic Life Support - American Heart Association, Basic Life Support - American Red Cross

Work Experience:
No specific work experience is required for this position.

Skills:
Not Applicable

Driver's License:
A driver's license is not required for this position.

More About This Job

Required Qualifications:

• Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).
• Some weekend and evening availability is required for this position.

Preferred Qualifications

Education:
Master's degree

Certifications /Professional Licenses :
No additional certification/professional licenses unless stated elsewhere in the job posting.

Work Experience:
No additional work experience unless stated elsewhere in the job posting.

Skills:
Clinical Research, Clinical Study Protocols, Communication, Computer Systems, Conducting Interviews, Data Compilation, Family Communication, Interpersonal Communication, Multitasking, Organizing, Research Support, Team Management, Working with Children

Grade
C09

Salary Range
$49,200.00 - $73,800.00 / Annually

The salary range reflects base salaries paid for positions in a given job grade across the University. Individual rates within the range will be determined by factors including one's qualifications and performance, equity with others in the department, market rates for positions within the same grade and department budget.

Questions

For frequently asked questions about the application process, please refer to our External Applicant FAQ.

Accommodation

If you are unable to use our online application system and would like an accommodation, please email [click to reveal email address] View email address on us.fitly.work or call the dedicated accommodation inquiry number at [click to reveal phone number]View phone number on us.fitly.work and leave a voicemail with the nature of your request.

All qualified individuals must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship.

Pre-Employment Screening
All external candidates receiving an offer for employment will be required to submit to pre-employment screening for this position. The screenings will include criminal background check and, as applicable for the position, other background checks, drug screen, an employment and education or licensure/certification verification, physical examination, certain vaccinations and/or governmental registry checks. All offers are contingent upon successful completion of required screening.

Benefits Statement

Personal

• Up to 22 days of vacation, 10 recognized holidays, and sick time.
• Competitive health insurance packages with priority appointments and lower copays/coinsurance.
• Take advantage of our free Metro transit U-Pass for eligible employees.
• WashU provides eligible employees with a defined contribution (403(b)) Retirement Savings Plan, which combines employee contributions and university contributions starting at 7%.

Wellness

• Wellness challenges, annual health screenings, mental health resources, mindfulness programs and courses, employee assistance program (EAP), financial resources, access to dietitians, and more!

Family

• We offer 4 weeks of caregiver leave to bond with your new child. Family care resources are also available for your continued childcare needs. Need adult care? We've got you covered.
• WashU covers the cost of tuition for you and your family, including dependent undergraduate-level college tuition up to 100% at WashU and 40% elsewhere after seven years with us.

For policies, detailed benefits, and eligibility, please visit:

EEO Statement
Washington University in St. Louis is committed to the principles and practices of equal employment opportunity. It is the University's policy to provide equal opportunity and access to persons in all job titles without regard to race, ethnicity, color, national origin, citizenship (where prohibited by federal law), age, religion, sex, sexual orientation, gender identity or expression, disability, protected veteran status, or genetic information.