Trabajos project manager en Ontario, California - Page 4Crear alertas

Job Description We are seeking a Construction Project Manager to join our team! You will oversee project planning, scheduling, estimating, take-offs, budgeting, implementation and ensure proper billings are generated on each project assigned. Responsibilities: • Oversee all aspects of construction project from planning to implementation, • Allocate resources for assigned projects, • Supervise onsite personnel and subcontractors, • Interface with project inspectors, contractors, architects, engineers, city and county officials, and clients, • Negotiate with contractors to receive reasonable order costs, • Aid in maximizing the profitability of the company by helping complete construction on time and on budget for the day-to-day operations of the construction site., • Maintain high standards of workmanship that adhere to original plans and specifications, • Train, evaluate, and discipline all subordinates to the position, in accordance with company policies and procedures., • Ensure project assistants receive proper and continuing training form all that senior them in job skills., • Create contracts and support information needed to secure work., • Monitor budgets and operational reports to determine that operations in your area of direct control are running at or below budget, make any changes needed to attain the costs and expense goals., • Review weekly assignments and staffing levels, report the status to the Director of Construction and/or President, for each job in accordance with company policies and procedures., • Previous experience in construction management or other related fields, • Familiarity with construction management software, specifically Procore, • Strong leadership qualities, • Strong negotiation skills, • Deadline and detail-orientedCompany DescriptionJones Covey Group, Inc. is a full-service fuel system contractor specializing in above and underground fuel systems for retail, commercial and government clients. JCGI is a national industry leader in fuel systems, fuel service stations, convenience stores, car washes, fuel facility service and environmental compliance nationally, providing services to Fortune 100 clients, major oil companies, distributors, fleet services, and local, state and federal agencies.Jones Covey Group, Inc. is a full-service fuel system contractor specializing in above and underground fuel systems for retail, commercial and government clients. JCGI is a national industry leader in fuel systems, fuel service stations, convenience stores, car washes, fuel facility service and environmental compliance nationally, providing services to Fortune 100 clients, major oil companies, distributors, fleet services, and local, state and federal agencies.

Job Description Summary: The Research Assistant (RA) works with Clinical Research Coordinators (CRC) and other team members and administers research study associated activities, assists in project planning, and ensures that pre-established work scope, study protocol, and regulatory requirements are followed. Additionally, RA recruits and coordinates research subjects, as appropriate, and serves as principle administrative liaison for the project. Duties and Responsibilities: The Research Assistant: • Attends Site Initiation Visits (SIV) to prepare for study initiation., • Assists Clinical Research Coordinators (CRCs) in developing source documentation for capturing data on study protocols., • Conducts an inventory of study materials and ensures availability for study activities., • Ensures all study-related training is completed in accordance with sponsor requirements for timely study initiation., • Inventories protocol shipments, including drugs, laboratory kits, and case report forms (CRFs)., • Maintains supplies for exam rooms and laboratories and ensures cleanliness., • Assists and/or works in the lab as needed., • Recruits study subjects appropriate for screening per protocol inclusion/exclusion criteria., • Ensures study enrollment goals are met as per sponsor requirements., • Schedules patient visits and prepares source documents for follow-up visits., • Assists in the completion of informed consent procedures following site SOPs and FDA/GCP guidelines., • Collects necessary laboratory specimens, EKGs, and subject questionnaires., • Performs research study visits as assigned., • Enters information into electronic data capture (EDC) systems., • Updates study logs, including screening, subject identification, and enrollment logs., • Updates the research Clinical Trial Management System (CTMS)., • Manages and organizes study files., • Maintains phone logs for communication with patients and trial sponsors., • Requests and organizes medical records when needed., • Prepares and maintains research binders and source documents., • Assists in preparing documents for submission to the sponsor and Institutional Review Board (IRB)., • Prepares lab shipments and ensures timely transportation to couriers., • Transports laboratory tubes and medications between the office and other site units., • Performs and documents vital assessments of patients., • Communicates with the central lab regarding abnormal lab values and notifies the manager of any significant findings., • Completes all study-specific training as assigned by sponsors or management., • Participates in site meetings and contributes relevant input., • Provides assistance and training to new and current staff members., • Collaborates with the Site Director, CRCs, and other team members to ensure smooth study operations., • Ensures confidentiality of participants’ health information and study-related data., • Occasional travel to company sites, investigator meetings, and/or company meetings., • Performs other job-related duties as assigned by the manager, CRCs, or other management team members., • Occasional travel to Company sites, Investigator meetings, and/or Company meetings. Requirements: • High School Diploma required., • IATA (dangerous goods handling), • GCP (good clinical practice), • BLS/Phlebotomist course, if required by your Manager., • CPR course, as arranged from time to time by the Company on-site., • Stericycle Trainings, first week of your hire date., • Excellent communication skills, • Problem Solving skills., • Planning /Organizational Skills, • Personal Motivation, • Customer Service Skills, • Understanding of ICH/GCP guidelines for human research, • Understanding of Code of Federal Regulations for Human Subject, • Computer Competency in Electronic Data Capture, • Laboratory Processing Procedures., • Prolonged periods of sitting at a desk and working on a computer., • Must be able to lift 20 pounds at times., • Exposure to human bodily fluids.