TriCore Reference Laboratories
Research Coordinator - Woodward/CT Research
TriCore Reference Laboratories, Albuquerque, New Mexico, United States, 87101
Overview
Research Coordinator - Woodward/CT Research at TriCore Reference Laboratories. This role involves managing many aspects of device trials, specimen procurement projects, consenting collections, and testing for research clients. Acts as central coordinator of study activity at the research site, liaising between the investigator and internal/external contacts. Responsibilities include pre-implementation and implementation activities such as feasibility discussions, contract and budget preparation, study startup, subject recruitment and enrollment, study maintenance, data management, and study closure. Participates as an effective team member in communications and operations. Schedule
Schedule: Monday-Friday 0800-1630 with other shifts as needed. Location
Woodward/CT Research Salary
Hourly Position Essential Functions
Review and evaluate protocols and requests with Principal Investigators (PI) and/or research team for feasibility. Create budgets for study or project and submit to appropriate process for review and approval. Prepare, implement, and assist in the approval of study start-up documents, worksheets, presentations, and activities. Serve as a liaison with study Principal Investigators and internal/external clients regarding study or project setup, logistics, and progress. Design data collection forms, such as case report forms (CRF), manifests, or sample accountability logs (SALs) as necessary. Handle inquiries regarding the protocol, case report forms, and other areas related to the study or project. Conduct subject interviews and obtain Informed Consent. Ensure timely and accurate completion and shipping of all study materials. Comply with documentation and procedural requirements including: case report form completion, enrollment reports, adverse events and dropout updates, handling and labeling of samples, and proper shipment of materials. Maintain quality assurance, regulatory documents, and reporting of study status information to verify data accuracy in the CRF. Coordinate with internal departments (e.g., Information Technology, Accounting, laboratory supervisors, managers, and technical staff) regarding research studies or projects. Participate in site audits by regulatory agencies when necessary. Ensure all study or project supplies are accounted for. Archive study documentation and correspondence. Training
Establish, maintain, and document training and competency programs for device trials or procurement projects. Schedule logistics meetings with the study team to ensure understanding of study workflow and workload. Inventory Control
Provide appropriate inventory control of study investigational use kits/reagents, study supplies, and study gift cards. Organizational / Employee Development
Organize daily work to meet study milestones or deadlines. Solicit staff input and feedback; listen to understand employee concerns and ideas. Support and implement department procedures, policies, and strategies aligned with corporate vision, values, and plans. Assist with marketing of section services through client contact, providing information for brochures, and tours to community groups as appropriate. Communicate with department management and staff to ensure information is shared. The above statements describe the general nature and level of work; this is not an exhaustive list of all responsibilities and duties. Minimum Education
Associates degree in a relevant field. Minimum Experience
One (1) year of relevant work experience in a healthcare or clinical laboratory setting. Preferences
Certification as a Research Coordinator. Patient or physician interaction experience. Clinical research experience. Knowledge of Salesforce, Compliance360, and Sunquest computer programs. Immunization Requirements
Provide documentation of hepatitis B immunity or vaccination, or sign a waiver refusing hepatitis immunization. Provide documentation of a PPD test conducted not more than 90 days prior to hire, or have a PPD test conducted. General Requirements
Working knowledge of statistical and variance analysis. Strong organization and attention to detail. Ability to communicate effectively with individuals from varying socio-economic and educational backgrounds. Ability to manage multiple projects simultaneously and meet deadlines. Ability to organize and direct workflow. Ability to develop budgets and monitor expenditures. Professional conduct when in the presence of subjects, peers, sponsors, monitors, or physicians. Ability to work independently and as part of a team; proficient with computers and basic word processing and spreadsheet programs. Seniority level
Entry level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
Hospitals and Health Care Referrals increase your chances of interviewing at TriCore Reference Laboratories. Get notified about new Researcher jobs in Albuquerque, NM.
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Research Coordinator - Woodward/CT Research at TriCore Reference Laboratories. This role involves managing many aspects of device trials, specimen procurement projects, consenting collections, and testing for research clients. Acts as central coordinator of study activity at the research site, liaising between the investigator and internal/external contacts. Responsibilities include pre-implementation and implementation activities such as feasibility discussions, contract and budget preparation, study startup, subject recruitment and enrollment, study maintenance, data management, and study closure. Participates as an effective team member in communications and operations. Schedule
Schedule: Monday-Friday 0800-1630 with other shifts as needed. Location
Woodward/CT Research Salary
Hourly Position Essential Functions
Review and evaluate protocols and requests with Principal Investigators (PI) and/or research team for feasibility. Create budgets for study or project and submit to appropriate process for review and approval. Prepare, implement, and assist in the approval of study start-up documents, worksheets, presentations, and activities. Serve as a liaison with study Principal Investigators and internal/external clients regarding study or project setup, logistics, and progress. Design data collection forms, such as case report forms (CRF), manifests, or sample accountability logs (SALs) as necessary. Handle inquiries regarding the protocol, case report forms, and other areas related to the study or project. Conduct subject interviews and obtain Informed Consent. Ensure timely and accurate completion and shipping of all study materials. Comply with documentation and procedural requirements including: case report form completion, enrollment reports, adverse events and dropout updates, handling and labeling of samples, and proper shipment of materials. Maintain quality assurance, regulatory documents, and reporting of study status information to verify data accuracy in the CRF. Coordinate with internal departments (e.g., Information Technology, Accounting, laboratory supervisors, managers, and technical staff) regarding research studies or projects. Participate in site audits by regulatory agencies when necessary. Ensure all study or project supplies are accounted for. Archive study documentation and correspondence. Training
Establish, maintain, and document training and competency programs for device trials or procurement projects. Schedule logistics meetings with the study team to ensure understanding of study workflow and workload. Inventory Control
Provide appropriate inventory control of study investigational use kits/reagents, study supplies, and study gift cards. Organizational / Employee Development
Organize daily work to meet study milestones or deadlines. Solicit staff input and feedback; listen to understand employee concerns and ideas. Support and implement department procedures, policies, and strategies aligned with corporate vision, values, and plans. Assist with marketing of section services through client contact, providing information for brochures, and tours to community groups as appropriate. Communicate with department management and staff to ensure information is shared. The above statements describe the general nature and level of work; this is not an exhaustive list of all responsibilities and duties. Minimum Education
Associates degree in a relevant field. Minimum Experience
One (1) year of relevant work experience in a healthcare or clinical laboratory setting. Preferences
Certification as a Research Coordinator. Patient or physician interaction experience. Clinical research experience. Knowledge of Salesforce, Compliance360, and Sunquest computer programs. Immunization Requirements
Provide documentation of hepatitis B immunity or vaccination, or sign a waiver refusing hepatitis immunization. Provide documentation of a PPD test conducted not more than 90 days prior to hire, or have a PPD test conducted. General Requirements
Working knowledge of statistical and variance analysis. Strong organization and attention to detail. Ability to communicate effectively with individuals from varying socio-economic and educational backgrounds. Ability to manage multiple projects simultaneously and meet deadlines. Ability to organize and direct workflow. Ability to develop budgets and monitor expenditures. Professional conduct when in the presence of subjects, peers, sponsors, monitors, or physicians. Ability to work independently and as part of a team; proficient with computers and basic word processing and spreadsheet programs. Seniority level
Entry level Employment type
Full-time Job function
Research, Analyst, and Information Technology Industries
Hospitals and Health Care Referrals increase your chances of interviewing at TriCore Reference Laboratories. Get notified about new Researcher jobs in Albuquerque, NM.
#J-18808-Ljbffr