Kalman & Co. Inc Work Values

Daily Duties at Kalman & Co. Inc:

As part of an integrated product team, my role consisted in extensive review of study protocols, informed consents, regulatory documentation for FDA submission, data listings, budgets. Participated in collaborations of formal review reports as requested by the government client. Reviewed and commented on contractors monthly progress reports to assure they were performing required tasks according to the project timeline. Reviewed proposals for alternate routes of drug administration. Reviewed and commented on multiple animal study protocols that were being conducted for data support to the clinical portion of the project.

What they like about Kalman & Co. Inc:

You highly value a work environment built on a formal structure, rules, and regulations. You do not enjoy the unpredictability of shifting priorities and deadlines that upset your routine. You require and enjoy direction, input and accountability as part of your work environment. You have a strong need to participate in making key decisions and feel left out if your superiors or co-workers do not seek your input when making decisions. You thrive on providing good customer service to both internal or external customers, and doing so makes you feel good.

Tags

Logistics, GCP, GLP, CRO, Clinical Specimen Management, Process Improvement, QA/QC, Regulatory Compliance, Operations Management, Training/Development, Procurement/Purchasing, Lab Inspections, Risk Management, Outsourcing, Cost Reduction, Vendor Relations, Instruction Manual Development, Consulting, Budgeting, Formulations Supervision, Start-ups/Turnarounds, Project Management, Reporting, Performance Management, Needs Assessment, Team Leadership/Motivation, Standard Operating Procedures, Visual Aid Creation, Clinical Study Evaluation/Workflow, Expense Control, Record Confidentiality, Lab Testing, Clinical Trial Expertise

Skills

Bilingual English/Spanish, Medical terminology, MS Office , Laboratory Inspection, Needs Assessment, Equipment Validation, Software Validation, Team Training, Team Leadership, Clinical Specimen management, Clinical Specimen Shipment, Laboratory Infrastructure Development, IVRS/WRS, FDA Regulations, Cost Reduction

These are some of the questions we asked our climbers about their experiences with Kalman & Co. Inc: