What are the responsibilities and job description for the Clinical Trials Assistant Coordinator-Urology position at UCLA Health?
Description
Under the direction of the CT Administrator, Faculty, Director, and Executive CAO, you will be responsible for assisting
in coordination of research activities for pharmaceutical/industry-sponsored, investigator-initiated, and NIH-sponsored clinical trials for the UCLA Institute of Urologic Oncology. Your key responsibilities include: resource planning, troubleshooting and coordinating efficient workflow and turnaround of pre-study tasks with other pre-award staff, and assisting with development of case report forms. This position requires a basic understanding of clinical trials coordination. Proficient computer skills are essential.
Contract, may become career
Salary range: $18.06-$35.78 HourlyQualifications
- Demonstrated clinical research experience, with basic knowledge of clinical urology, including working knowledge of good clinical practices for clinical research.
- Ability to work in more than one environment, travels to participating hospitals, and attend off site staff meetings, conferences, and investigator meetings.
- Demonstrated organizational skills to handle multiple clinical research projects for efficiency and cost-effectiveness, including handling work delegated by more than one individual.
- Experience in performing evaluations and interventions under the direction of the Principal Investigator with acutely ill oncology patients using strong clinical judgment and up to date oncology knowledge.
- Ability to work flexible hours to accommodate research procedures and deadlines.
- Excellent English verbal and writing communication skills to covey and obtain information to and from investigators, patients, families, sponsors and co-workers.
- Problem solving skill to work effectively, meet research goals, with minimal supervision.
- Demonstrated computer skills using Word, Excel, e-mail, UCLA HER System and databases to create reports, correspondence, and other documents as required.
- Ability to collect from data management personnel, data collection and management activities.
- Skill in preparation of accurate and timely annual reports and statistical information on all protocols as needed.
- Bachelor's Degree strongly preferred
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.
Under the direction of the CT Administrator, Faculty, Director, and Executive CAO, you will be responsible for assisting
in coordination of research activities for pharmaceutical/industry-sponsored, investigator-initiated, and NIH-sponsored clinical trials for the UCLA Institute of Urologic Oncology. Your key responsibilities include: resource planning, troubleshooting and coordinating efficient workflow and turnaround of pre-study tasks with other pre-award staff, and assisting with development of case report forms. This position requires a basic understanding of clinical trials coordination. Proficient computer skills are essential.
Contract, may become career
Salary range: $18.06-$35.78 HourlyQualifications
- Demonstrated clinical research experience, with basic knowledge of clinical urology, including working knowledge of good clinical practices for clinical research.
- Ability to work in more than one environment, travels to participating hospitals, and attend off site staff meetings, conferences, and investigator meetings.
- Demonstrated organizational skills to handle multiple clinical research projects for efficiency and cost-effectiveness, including handling work delegated by more than one individual.
- Experience in performing evaluations and interventions under the direction of the Principal Investigator with acutely ill oncology patients using strong clinical judgment and up to date oncology knowledge.
- Ability to work flexible hours to accommodate research procedures and deadlines.
- Excellent English verbal and writing communication skills to covey and obtain information to and from investigators, patients, families, sponsors and co-workers.
- Problem solving skill to work effectively, meet research goals, with minimal supervision.
- Demonstrated computer skills using Word, Excel, e-mail, UCLA HER System and databases to create reports, correspondence, and other documents as required.
- Ability to collect from data management personnel, data collection and management activities.
- Skill in preparation of accurate and timely annual reports and statistical information on all protocols as needed.
- Bachelor's Degree strongly preferred
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.
Clinical Trials Regulatory Coordinator - Urology
University of California - Los Angeles Health -
Los Angeles, CA
Clinical Research Coordinator-Urology
UCLA Health Careers -
Los Angeles, CA
Assistant Professor of Clinical Urology-Bakersfield
Keck School of Medicine -
Los Angeles, CA
