Research Associate I

Purpose Of Role / Job Summary

The Research Associate I assists the Study Director team with the planning, execution, data tabulation, and reporting of Good Laboratory Practices (GLP) and non-GLP Toxicology, Medical Device and Pharmacokinetic studies. To perform this job successfully, an individual must have the knowledge, skills, and abilities identified below and perform each essential duty and responsibility satisfactorily, either with or without reasonable accommodation.

Key Accountabilities

• 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.
• Affords assistance with the review of study event schedules as needed in accordance with the study protocol.
• Affords assistance to the Study Directors in coordination and oversight of study conduct and ensuring proper raw data collection according to the study protocol and applicable standard operating procedures (SOPs) with minimal supervision.
• Participates in scribing and data collection for study activities both in an electronic data capture system, and on raw data forms.
• Affords assistance in inventory and tracking of Test and Control devices and/or materials.
• Downloads electronic data reports, compiles raw data packages, analyzes study data and creates data tables and graphs.
• Affords assistance in preparation and review of study reports.
• Affords assistance in quality control (QC) of tabulated data.
• Prepares or affords assistance in the preparation of internal and/or contracted sub-reports as required.
• Affords assistance in archiving of finalized study data.
• Efficiently and effectively communicates to supervisor, study directors, and study personnel when issues arise that impact project progress or timing.
• Provides peer review of study protocols and associated amendments, SOPs, reports, animal use activity and other documentation.

Critical Success Factors

• Good organizational skills and detail oriented.
• Excellent communication and interpersonal skills with ability to work with personnel at all levels of the organization.
• 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 minimal supervision.
• Working knowledge and awareness of general laboratory procedures.
• Ability to follow detailed instructions with a sense for scientific method.

Minimum Requirements

• Associate degree, or equivalent, in biology or life science.
• One year experience in a laboratory, contract research organization, or similar research setting.
• 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.

Preferred

• Bachelor’s degree in biology or life science.

Physical Requirements

• Occasionally lift up to fifty (50) pounds and move heavy equipment in a safe manner.
• Communicate via telephone and face-to-face.
• Stand and move (e.g., walk, bend, reach, lift, crouch, push, pull, lift.) throughout an entire work shift.
• Manual dexterity (e.g., feeling, grasping, typing, repetitive motion) to operate necessary equipment and perform essential tasks outlined in position description.
• 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).
• Utilization of supplied personal protection equipment (PPE).
• Exposure to potential hazards such as hot water, steam, mechanical equipment, biological substances, loud noise, odors, chemicals, and range of outdoor weather conditions.
• Regular on-site attendance as scheduled by management.
• Ability to travel to various site locations.

Salary Range

$21-$25/hr. The salary range may adjust based on the candidate's relevant experience and/or education level.

Benefits

• Health and dental coverage.
• Short- and long-term disability.
• Paid time off.
• Paid parental leave.
• 401K.

About Inotiv

Inotiv is a growing contemporary drug discovery and development company where we "Play to Win" in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There’s an opportunity for everyone at all phases of a career, each individual’s unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people’s lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world.

EEO Statement

Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.