Research Coordinator - CHAMP Clinic - UCLA Health
Los Angeles, CA
About the Job
Description
The Semel Insititute is seeking a part time Assistant Clinical Research Coordinator to provide research support for the Child & Adolescent Bipolar Mood Disorders Program (CHAMP) in the Semel Institute's Child and Adolescent Psychiatry Division. Major functions include screening potential study participants, scheduling, consenting, and completing assessments for the research programs being conducted in the clinic, as well as basic administrative duties relevant to this research (faxing, coping, coordination with providers, data entry). The person will be working to set up and run a newly funded study- "A Ketogenic Diet Approach to Bipolar Disorder in Adolescents"- which is a 2 year, multi-site study of adolescents and young adults with bipolar disorder. In this role you will be responsible for participant recruitment, consenting, managing participant follow up appointments, scheduling of interviews, and reliability checks. In addition you will also meet regularly with coordinators of other research sites to ensure consistency between teams, organize research data, and provide updated reports to investigators at bi-weekly all site meetings.
Pay Range: $27.08 - $43.55 hourly
Qualifications
Required:
+ Minimum of 1+ years of experience in a clinical research setting
+ Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as member of a team.
+ Ability to effectively communicate to and interact with patients in a compassionate and kind manner.
+ Ability to set priorities and complete ongoing tasks with competing deadlines, with frequent interruptions, to meet the programmatic and department needs, while complying
+ with applicable University policies and federal and state regulations.
+ Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.
+ Close attention to detail to ensure accuracy in a fast-paced, fluctuating workload environment.
+ Organization skills to create and maintain administrative and regulatory files effectively as well as independently balance the various tasks to ensure deadlines are met.
+ Demonstrated proficiency with Adobe and Microsoft suite software, especially Excel, to perform daily tasks efficiently and accurately.
+ A learning and professional growth mentality so that new software tools, systems, and processes can be adopted quickly and efficiently.
+ Working knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws.
+ Knowledge of and experience working with a variety of local and external IRBs, scientific review and other research committees, national cooperative group sponsors, industry sponsors, federal and foundation funding organizations, etc.
+ Strong verbal and written communication skills to effectively establish rapport, building collaborative relationships, and communicate complex concepts and ideas in an easy-to- understand manner
+ Ability to adapt to changing job demands and priorities, remain flexible including working flexible hours to accommodate research deadlines.
+ Ability to handle confidential information with judgement and discretion.
+ High degree of concentration and focus in a work environment that contains distracting stimuli, competing deadlines, and work delegated by more than one individual.
+ Availability to work in more than one environment, travelling to various clinic sites, meetings, conferences, etc.
Preferred:
+ Bachelor's degree
UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.
The Semel Insititute is seeking a part time Assistant Clinical Research Coordinator to provide research support for the Child & Adolescent Bipolar Mood Disorders Program (CHAMP) in the Semel Institute's Child and Adolescent Psychiatry Division. Major functions include screening potential study participants, scheduling, consenting, and completing assessments for the research programs being conducted in the clinic, as well as basic administrative duties relevant to this research (faxing, coping, coordination with providers, data entry). The person will be working to set up and run a newly funded study- "A Ketogenic Diet Approach to Bipolar Disorder in Adolescents"- which is a 2 year, multi-site study of adolescents and young adults with bipolar disorder. In this role you will be responsible for participant recruitment, consenting, managing participant follow up appointments, scheduling of interviews, and reliability checks. In addition you will also meet regularly with coordinators of other research sites to ensure consistency between teams, organize research data, and provide updated reports to investigators at bi-weekly all site meetings.
Pay Range: $27.08 - $43.55 hourly
Qualifications
Required:
+ Minimum of 1+ years of experience in a clinical research setting
+ Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as member of a team.
+ Ability to effectively communicate to and interact with patients in a compassionate and kind manner.
+ Ability to set priorities and complete ongoing tasks with competing deadlines, with frequent interruptions, to meet the programmatic and department needs, while complying
+ with applicable University policies and federal and state regulations.
+ Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.
+ Close attention to detail to ensure accuracy in a fast-paced, fluctuating workload environment.
+ Organization skills to create and maintain administrative and regulatory files effectively as well as independently balance the various tasks to ensure deadlines are met.
+ Demonstrated proficiency with Adobe and Microsoft suite software, especially Excel, to perform daily tasks efficiently and accurately.
+ A learning and professional growth mentality so that new software tools, systems, and processes can be adopted quickly and efficiently.
+ Working knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws.
+ Knowledge of and experience working with a variety of local and external IRBs, scientific review and other research committees, national cooperative group sponsors, industry sponsors, federal and foundation funding organizations, etc.
+ Strong verbal and written communication skills to effectively establish rapport, building collaborative relationships, and communicate complex concepts and ideas in an easy-to- understand manner
+ Ability to adapt to changing job demands and priorities, remain flexible including working flexible hours to accommodate research deadlines.
+ Ability to handle confidential information with judgement and discretion.
+ High degree of concentration and focus in a work environment that contains distracting stimuli, competing deadlines, and work delegated by more than one individual.
+ Availability to work in more than one environment, travelling to various clinic sites, meetings, conferences, etc.
Preferred:
+ Bachelor's degree
UCLA Health welcomes all individuals, without regard to race, sex, sexual orientation, gender identity, religion, national origin or disabilities, and we proudly look to each person’s unique achievements and experiences to further set us apart.
Source : UCLA Health
