Role overview

Qualifications

BS or equivalent in natural sciences
Experience supporting Non-GLP and GLP non-clinical toxicology studies is preferred
Excellent scientific writing and documentation skills
Ability to work independently and in a fast-paced CRO environment

Responsibilities

Generation of study protocol based on the signed study proposal
Generation of protocol amendments, if and when needed
Scheduling and conducting the study start meetings
Coordinate client visits, when requested by the client

Key facts

Remote from: Illinois (USA)
Full time
Conference Coordinator
English

Hard skills

Toxicological Chemistry Scientific Writing Regulatory Compliance

Other skills

Collaboration
Time Management

About the company

Frontage Laboratories, Inc

Pharmaceuticals

Frontage Laboratories, Inc. is a CRO that provides integrated, science-driven, product development services throughout the drug discovery and development process to enable pharmaceutical and biotechnology companies to achieve their development goals. Comprehensive services include drug metabolism and pharmacokinetics, analytical testing and formulation development, preclinical and clinical trial material manufacturing, bioanalysis, preclinical safety and toxicology assessment and early phase clinical studies. Frontage has enabled many biotechnology companies and leading pharmaceutical companies of varying sizes to advance a myriad of molecules through development and file regulatory submissions in the United States, China and other countries.

Company details

Company typeSME

IndustryPharmaceuticals

Company size501 - 1000

Links

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Job description

Study Coordinator

Title: Study Coordinator

Location: Chicago, IL (on-site)

Reports to: Director Laboratory Operations

Full-time

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Our Chicago, IL site provides toxicology testing and research laboratory services and specialized pre-clinical studies in support of pharmaceutical and biotechnology products.

Position/Job Summary

The individual in this position is involved in studies that evaluate the safety and/or toxicity of various materials (e.g., pharmaceuticals, chemicals, etc.). This position demands to be an active member of the study team and work along with the Study Directors and Report Writers and report to the Team Lead of Study Coordination group. This is a full-time on‑site position at our Chicago facility with no provisions for working remotely.

Roles and Responsibilities

Frontage Laboratories is seeking a highly motivated individual supporting Study Team for the non-clinical toxicology studies conducted under GLP regulations.

Key Responsibilities

Generation of study protocol based on the signed study proposal
Generation of protocol amendments, if and when needed
Scheduling and conducting the study start meetings
Coordinate client visits, when requested by the client

Generating data tables from Provantis
Collaborate with other units to support study timelines
Interact with Study Directors and help define study priorities and schedules
Demonstrates the ability to contribute to the success of assignments
Performs other duties as assigned

Qualifications and Experience

BS or equivalent in natural sciences.
Experience supporting Non-GLP and GLP non-clinical toxicology studies is preferred.
Excellent scientific writing and documentation skills.

Ability to work independently and in a fast-paced CRO environment.
Familiarity with FDA, OECD, and GLP regulatory requirements is preferred.

Salary: $21.64-26.45/hour, negotiable based on experience.

Benefits

401k Employer Match with immediate vesting
Vision Insurance
Medical and Dental Insurance with multiple coverage options
FSA (Medical, Dependent Care, and Commuter)
Short Term Disability
Long Term Disability
Life Insurance
Generous Paid Holidays and PTO

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.