National Medical Association
Laboratory Center Project Manager - Pediatrics
National Medical Association, Los Angeles, California, United States, 90079
Description
The Division of Pediatric Infectious Diseases within the David Geffen School of Medicine at UCLA seeks an ACTG/IMPAACT Laboratory Center Project Manager to join their Clinical Trials Laboratory Center. The Laboratory Center Project Manager will work closely with Protocol Team Leadership to implement clinical trials protocols and coordinate laboratory-related committees and working groups. The Laboratory Center Project Manager will also review protocol testing, laboratory quality assurance information, and support capabilities required to conduct global clinical trials.Annual Salary Range: $83,800 - $179,400
Qualifications
All Required:
Bachelor’s degree required, Master’s degree preferredMinimum of 4+ years of experience in a clinical regulatory roleExpert knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and lawsIn depth 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.Demonstrated analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actionsDemonstrated experience with FDA processes and proceduresInterpersonal 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 a member of a teamAbility 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 regulationsClose attention to detail to ensure accuracy in a fast-paced, fluctuating workload environmentOrganization skills to create and maintain administrative and regulatory files effectively as well as independently balance the various tasks to ensure deadlines are metDemonstrated 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 efficientlyDemonstrated analytical skills to address problems of high complexityAbility to think creatively to develop solutions affecting the full team
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The Division of Pediatric Infectious Diseases within the David Geffen School of Medicine at UCLA seeks an ACTG/IMPAACT Laboratory Center Project Manager to join their Clinical Trials Laboratory Center. The Laboratory Center Project Manager will work closely with Protocol Team Leadership to implement clinical trials protocols and coordinate laboratory-related committees and working groups. The Laboratory Center Project Manager will also review protocol testing, laboratory quality assurance information, and support capabilities required to conduct global clinical trials.Annual Salary Range: $83,800 - $179,400
Qualifications
All Required:
Bachelor’s degree required, Master’s degree preferredMinimum of 4+ years of experience in a clinical regulatory roleExpert knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and lawsIn depth 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.Demonstrated analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actionsDemonstrated experience with FDA processes and proceduresInterpersonal 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 a member of a teamAbility 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 regulationsClose attention to detail to ensure accuracy in a fast-paced, fluctuating workload environmentOrganization skills to create and maintain administrative and regulatory files effectively as well as independently balance the various tasks to ensure deadlines are metDemonstrated 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 efficientlyDemonstrated analytical skills to address problems of high complexityAbility to think creatively to develop solutions affecting the full team
#J-18808-Ljbffr