Inotiv provides biopharmaceutical analytical, reproductive toxicology, medical device testing, DMPK, consulting and pathological services. The Research Associate I assists the Study Director with planning, execution, data tabulation, and reporting of GLP and non-GLP studies, ensuring adherence to protocols and quality control of data.
Responsible for the preparation of study notebooks.
Creates and reviews raw data collection forms for adherence to protocol and clarity/efficacy prior to study start.
Assists with the creation and review of study event calendars/schedules.
Confirms study activities are scheduled with the in-life team as described by the protocol.
Assists the Study Directors in coordinating study conduct and ensuring proper raw data collection according to the study protocol and applicable standard operating procedures (SOPs).
Assists in the oversight of various aspects of study conduct with minimal supervision, as needed, and trained.
Participates in scribing for study activities as needed and trained, both in an electronic data capture system, and on raw data forms.
Performs quality control (QC) of tabulated data.
Downloads electronic data reports and compiles raw data packages.
Assists with the compilation and analysis of data and creation of data tables/graphs.
Assists with preparation and review of study reports.
Archiving of finalized study data.
Follows all SOPs and other applicable laboratory or company policies and procedures.
Maintains confidential information.
Supports and participates in company initiatives as directed.
Performs periodic review of all applicable SOPs to ensure accuracy and confirm procedures are being performed according to SOPs.
Participates in SOP writing, reviews, and revisions, as needed.
Completes training requirements as assigned and maintains appropriate training documentation.
Maintains compliance and adheres to all safety regulations, policies, and procedures and good documentation practices.
Maintains a thorough knowledge and ensures compliance with GLP, United States Department of Agriculture (USDA), Association of Assessment and Accreditation of Laboratory Animal Care (AAALAC), Office of Laboratory Animal Welfare (OLAW), and other applicable regulations.
Interacts with clients, other employees, and the community in a professional manner.
Performs other duties as assigned.
Qualification
Required
Good organizational skills and detail oriented.
Excellent communication and interpersonal skills with ability to work with personnel at all levels of the organization.
Must have the ability to work independently as well as a team environment.
Ability to multi-task and prioritize tasks in a high energy, fast paced environment.
Exhibits accuracy and adaptability performing laboratory operations, some of which may be difficult and/or non-routine.
Proficient in the use of a computer to compile and maintain simple data, spreadsheets, checklists and reports for records and inventory, utilizing the appropriate software.
Exhibits an aptitude for quality, an eye for detail, the ability to follow written instructions and work with a minimum of supervision.
Displays a basic understanding of GLP, AAALAC, OLAW, and USDA Animal and Plant Health Inspection Service (APHIS) regulations and standards with the ability to apply these practices daily.
Demonstrates a working knowledge and awareness of general laboratory procedures. Maintains a commitment to adhere to all safety regulations and procedures.
Demonstrates an ability to follow detailed instructions with a sense for scientific method.
Bachelor’s degree in biology or life science with one-year direct laboratory animal work experience, or Associate degree, or equivalent, in biology or life science with at least two years of direct laboratory animal work experience, or three years of direct laboratory animal work experience without a college science degree, or equivalent combination of related education and required work experience will be considered with management approval.
Excellent written and verbal communication skills.
Familiarity with writing and interpreting scientific reports and data.
Demonstrated proficiency using Microsoft Excel and other Office Suite products and Adobe Acrobat. Ability to quickly learn new computer software systems.
Ability to regularly lift up to fifty (50) pounds and move heavy equipment in a safe manner.
Ability to communicate via telephone and face-to-face.
Ability to stand and move (e.g., walk, bend, reach, lift, crouch, push, pull, lift.) throughout an entire work shift.
Manual dexterity (e.g., feeling, grasping, fingering, repetitive motion) to operate necessary equipment and perform essential tasks outlined in position description.
Required to have close visual acuity (e.g., preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; visual inspection involving small parts) and depth perception (with or without glasses/contacts).
Required utilization of supplied personal protection equipment (PPE).
Occasional exposure to potential hazards such as hot water, steam, mechanical equipment, biological substances, loud noise, odors, chemicals, and to range of outdoor weather conditions.
Regular on-site attendance as scheduled by management.
Preferred
Benefits
Health and dental coverage
Short- and long-term disability
Paid time off
Paid parental leave
401K
And more!
Inotiv provides biopharmaceutical analytical, reproductive toxicology, medical device testing, DMPK, consulting and pathological services.
