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Training Specailist (All Levels)

Altasciences


Job Location:

Columbia, SC - USA

Monthly Salary: Not provided by the employer
Posted: 20 September 2026 (2 days ago)
Application Deadline: 18 December 2026
Vacancies: 1 Vacancy

Job Summary

About the Role
Works under limited supervision and supports the department by providing the development coordination and assurance of GLP compliant training procedures and practices. Works as delegated by department management to ensure the successful completion of training activities and maintenance of technical skills. Provides administrative and organizational support in training planning scheduling coordination document management and reporting. Performs quality control (QC) and/or maintenance of plans SOPs worksheets raw data study binders and data archiving. May provide support for other work groups as needed.


What Youll Do Here
Develop and implement Standard Operating Procedures and qualification requirements ensuring compliance with FDA (GLP) L&I and other regulatory agencies
Research new procedures train and oversee their implementation
Coordinate with department trainers and management to schedule training and cross training
Train and cross train in the technical execution of current protocols and standard operating procedures (SOPs) daily activities associated with all functions of the department and other related services
Help identify training staff and ensures uniform training content across all trainer staff
Responsible for the development and maintenance of training programs and may assist with the creation and maintenance of training forms or electronic records
Focus on process management and standardization to improve efficiency and quality
Determine proper documentation of training procedures and data acquisition in an effort to accurately document compliance with plans SOPs and Protocols while facilitating the needs of department management
Work with all groups to improve processes
Monitor and communicate training deadlines to ensure adherence to set schedules
Communicate training deadlines to study personnel and department management
Track milestones and ensure training schedules are up to date
Manage the timely review and assembly of training documentation
Assign and oversee duties to personnel necessary to complete training objectives
Provide hands-on training of staff for classes and technical skills and assesses competency
Respond to Quality Assurance audits for training processes and corrective actions that require training
Perform QC review of data in a timely manner
Work with different departments to help ensure consistency of training practices and organization
Support and participate in study procedures if necessitated by workload
Supervise studies procedures and research assignments and coordinate duties of personnel and study teams
Participate in evaluation performance or maintenance of new systems or equipment
Maintain general organization and cleanliness of work area including cleaning and disinfecting procedure rooms and preparation areas

What Youll Need to Succeed
BA/BS in biological sciences or related science degree; education may be substituted with related laboratory experience and administrative skills

2 years working in a vivarium setting required
1 years staff training experience required
3 years working in a research or regulated environment preferred
Professional certification in area of expertise preferred
Intermediate computer skills including proficiency with Microsoft Office suite
English proficiency both written and verbal; general reading writing and verbal communication skills
Intermediate maths skills
Ability to work cross functionally on process improvements
Practical problem solving skills and can deal with a variety of concrete variables
Interpret a variety of instructions furnished in written oral diagram or schedule form
Demonstrate attention to detail

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About Company

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Contract research organization specialized in seamless, end-to-end, early phase drug development, we act to get your most promising compounds into and through early phase clinical trials.

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