University of California, Davis
Sr. Clinical Research Coordinator
University of California, Davis, Sacramento, California, United States, 95828
Overview
Join to apply for the
Sr. Clinical Research Coordinator
role at
University of California, Davis . Job Summary: Under general direction of Clinical Research Supervisor, the Senior Clinical Research Coordinator has an advanced-level working knowledge of data management activities, strong communication skills and the ability to work in a team environment to independently coordinate, direct, and ensure follow-through for overall administration and outcome of multiple clinical studies. This position may include oversight and training of new or lower-level clinical research coordinators and/or other support personnel, coordinate research meetings and act as a resource. This is a 100% position that will work with the PIs, other department personnel, sponsors, and community physicians to support and provide guidance on the administration of regulatory coordination, data management, compliance, patient navigation, personnel and other related aspects of oncology and transplant-related clinical studies. This is a grant-funded position. Responsibilities
75% - Clinical Trial Management 15% - Patient advocate/Navigator 5% - Regulatory 5% - Continuing Education Qualifications
Bachelor\'s degree in related field and/or equivalent experience/training Five or more years of experience in Industry Sponsored Clinical Trial processes; clinical and regulatory Three or more years of experience in stem cell or oncology clinical trials Extensive knowledge of FDA and IRB regulations, ICH guidelines and current Good Clinical Practice (cGCP) Advanced knowledge and skills using Clinical Trial Management System; Velos or OnCore Advanced computer systems and database skills, including Windows, Microsoft Office Suite, electronic medical records, and electronic data capture systems for clinical research Demonstrated ability to communicate effectively and engage in collaborative problem-solving and negotiation with staff and colleagues Ability to work independently with minimal supervision and handle changing priorities and deadlines Strong judgment, initiative and resourcefulness in decision-making Oral communication and interpersonal skills to effectively correspond with the general public, co-workers, physicians, patients, caregivers, clinic staff and other health care professionals Organizational skills and attention to detail to maintain large volumes of records and manage workload priorities Ability to multi-task and work cooperatively as part of a diverse team Extensive knowledge of clinical trial management Preferred Qualifications
Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals Advanced knowledge of basic anatomy, medical terminology and ability to interpret physicians\' notes, medical records, laboratory and scan results Advanced knowledge and understanding of oncology and disease processes as applied to clinical research Department Overview
The UC Davis Alpha Stem Cell Clinic (ASCC) specializes in early phase, first-in-human trials. The Alpha Stem Cell Clinic is devoted to accelerating the translation of stem cell and regenerative medicine research to safe and effective therapies, attracting patients, funding agencies and study sponsors to participate in and support stem cell and gene therapy trials. Position Information
Salary or Pay Range: $38.85 - $62.47 Salary Frequency: Hourly Salary Grade: 100 UC Job Title: CLIN RSCH CRD SR NEX UC Job Code: 007889 Number of Positions: 1 Appointment Type: Staff: Career Percentage of Time: 100% Shift (Work Schedule): Day Location: UCD Institute for Regenerative Cure (HSP041) Union Representation: RX-Research Professionals Benefits Eligible: Yes This position is 100% on-site This is not an H-1B opportunity Benefits
UC Davis offers a full range of benefits, resources and programs to support health, wellness, financial and career goals. Details are provided by the Benefits pages and contracts. Union-negotiated benefits apply as applicable. Work Environment & Requirements
Extended hours at computer; general schedule 8-5 M-F with flexibility for patient needs; occasional overtime and weekends may be required; regular travel for training and conferences; walking between sites on campus. Special Requirements
This is a critical position, as defined by UC Policy; employment is contingent upon criminal background check(s) and may include drug screening, medical evaluation clearance and functional capacity assessment Mandated reporter under CANRA; compliance with applicable policies, procedures and training N/A A Culture of Opportunity and Belonging: UC Davis is an Equal Opportunity Employer; all qualified applicants will be considered regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age or protected veteran status.
#J-18808-Ljbffr
Join to apply for the
Sr. Clinical Research Coordinator
role at
University of California, Davis . Job Summary: Under general direction of Clinical Research Supervisor, the Senior Clinical Research Coordinator has an advanced-level working knowledge of data management activities, strong communication skills and the ability to work in a team environment to independently coordinate, direct, and ensure follow-through for overall administration and outcome of multiple clinical studies. This position may include oversight and training of new or lower-level clinical research coordinators and/or other support personnel, coordinate research meetings and act as a resource. This is a 100% position that will work with the PIs, other department personnel, sponsors, and community physicians to support and provide guidance on the administration of regulatory coordination, data management, compliance, patient navigation, personnel and other related aspects of oncology and transplant-related clinical studies. This is a grant-funded position. Responsibilities
75% - Clinical Trial Management 15% - Patient advocate/Navigator 5% - Regulatory 5% - Continuing Education Qualifications
Bachelor\'s degree in related field and/or equivalent experience/training Five or more years of experience in Industry Sponsored Clinical Trial processes; clinical and regulatory Three or more years of experience in stem cell or oncology clinical trials Extensive knowledge of FDA and IRB regulations, ICH guidelines and current Good Clinical Practice (cGCP) Advanced knowledge and skills using Clinical Trial Management System; Velos or OnCore Advanced computer systems and database skills, including Windows, Microsoft Office Suite, electronic medical records, and electronic data capture systems for clinical research Demonstrated ability to communicate effectively and engage in collaborative problem-solving and negotiation with staff and colleagues Ability to work independently with minimal supervision and handle changing priorities and deadlines Strong judgment, initiative and resourcefulness in decision-making Oral communication and interpersonal skills to effectively correspond with the general public, co-workers, physicians, patients, caregivers, clinic staff and other health care professionals Organizational skills and attention to detail to maintain large volumes of records and manage workload priorities Ability to multi-task and work cooperatively as part of a diverse team Extensive knowledge of clinical trial management Preferred Qualifications
Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals Advanced knowledge of basic anatomy, medical terminology and ability to interpret physicians\' notes, medical records, laboratory and scan results Advanced knowledge and understanding of oncology and disease processes as applied to clinical research Department Overview
The UC Davis Alpha Stem Cell Clinic (ASCC) specializes in early phase, first-in-human trials. The Alpha Stem Cell Clinic is devoted to accelerating the translation of stem cell and regenerative medicine research to safe and effective therapies, attracting patients, funding agencies and study sponsors to participate in and support stem cell and gene therapy trials. Position Information
Salary or Pay Range: $38.85 - $62.47 Salary Frequency: Hourly Salary Grade: 100 UC Job Title: CLIN RSCH CRD SR NEX UC Job Code: 007889 Number of Positions: 1 Appointment Type: Staff: Career Percentage of Time: 100% Shift (Work Schedule): Day Location: UCD Institute for Regenerative Cure (HSP041) Union Representation: RX-Research Professionals Benefits Eligible: Yes This position is 100% on-site This is not an H-1B opportunity Benefits
UC Davis offers a full range of benefits, resources and programs to support health, wellness, financial and career goals. Details are provided by the Benefits pages and contracts. Union-negotiated benefits apply as applicable. Work Environment & Requirements
Extended hours at computer; general schedule 8-5 M-F with flexibility for patient needs; occasional overtime and weekends may be required; regular travel for training and conferences; walking between sites on campus. Special Requirements
This is a critical position, as defined by UC Policy; employment is contingent upon criminal background check(s) and may include drug screening, medical evaluation clearance and functional capacity assessment Mandated reporter under CANRA; compliance with applicable policies, procedures and training N/A A Culture of Opportunity and Belonging: UC Davis is an Equal Opportunity Employer; all qualified applicants will be considered regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age or protected veteran status.
#J-18808-Ljbffr