Associate Director, Inlife Operations

Frontage Laboratories; Chicago (IL); Sur place; USD 90 000 - 130 000; Plein temps

Avantages offerts par ce poste

401k Employer Match with immediateVest

Vision Insurance

Medical and Dental Insurance with mult

FSA (Medical, Dependent Care, and Comn

Short Term Disability

Long Term Disability

Life Insurance

Generous Paid Holidays and PTO

Résumé du poste

Frontage Laboratories, a leading CRO, seeks an experienced Associate Director of Inlife Operations at our Chicago site. You will lead the Inlife Operations team, optimizing schedules, training staff, and ensuring GLP-compliant study execution.

The role drives site growth by expanding technical capabilities, coordinating across departments, and delivering high-quality, timely nonclinical toxicology studies to clients. Strong leadership and cross-functional collaboration are essential.

Qualifications

• Bachelor’s degree in Animal Science, Biology, Toxicology or related field required; advanced degree preferred.
• 15+ years in nonclinical toxicology/preclinical research, GLP-regulated CRO experience advantageous.
• Minimum 10 years in supervisory/management roles overseeing inlife operations.
• Experience managing personnel, coordinating multiple studies, and optimizing resources.
• Strong knowledge of GLP requirements and animal welfare regulations.
• Experience with complex inlife procedures (dosing, clinical observations, sampling, termination).
• Proven ability to develop training programs, manage schedules, and implement process improvements.
• Ability to lead teams and resolve operational challenges across departments.

Responsabilités

• Provide leadership and supervision of the Inlife Operations team across multiple studies.
• Ensure timely, high-quality execution of inlife activities in several concurrent non-clinical studies.
• Develop macro- and micro-schedules for inlife operations and resource planning.
• Coordinate scheduling with study teams and supporting staff.
• Establish and maintain a comprehensive training program for inlife personnel.
• Ensure staff are trained and qualified for assigned procedures and studies.
• Identify training gaps and implement competency improvements.
• Identify opportunities to improve efficiency, productivity, and resource use.
• Develop standardized workflows and SOPs for inlife activities.
• Ensure compliance with study protocols, GLP requirements, and regulations.
• Promote a quality culture with timely documentation.

Connaissances

Leadership

Scheduling

Training

Cross-functional collaboration

Formation

Bachelor's degree in Animal Science/Biology/Toxicology

Advanced degree preferred

Description du poste

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Associate Director, Inlife Operations

Safety & Tox - Experimur Full Time Chicago, IL, US

Salary Range: $90,000.00 To $130,000.00 Annually

Job Title: Associate Director, Inlife Operations
Location: Chicago, IL
Reports to: Vice President of Safety and Toxicology

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, Europe, and Asia. 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 site provides services for general toxicology, developmental and reproductive toxicology (DART), juvenile, dermal, ocular, and carcinogenicity studies in support of pharmaceutical and biotechnology products.

Position Summary:
Frontage Laboratories is seeking an experienced and highly motivated Associate Director of inlife operations. Person in this position is responsible for the overall leadership, management, and development of the Inlife Operations team within a nonclinical toxicology Contract Research Organization (CRO).

This leadership role will be responsible for macro- and micro-scheduling of study activities, optimizing resource utilization, developing and training the inlife team, and drive continuous improvement in operational efficiency. The role will also focus on expanding the site's technical capabilities, supporting business growth, and serving as a key communication link between the inlife team and site management.

The successful candidate will be a strong operational leader with excellent organizational, communication, and problem-solving skills, and a demonstrated commitment to employee development, scientific quality, and client satisfaction.

Key Responsibilities:

• Provide overall leadership and supervision of the Inlife Operations team, including technicians, supervisors, managers, and other inlife personnel.
• Ensure the timely and high-quality execution of inlife activities across multiple concurrent non-clinical toxicology studies.
• Develop and maintain macro- and micro-schedules for inlife operations, including study initiation, animal receipt and acclimation, dosing, clinical observations, procedures, sample collection, and study termination activities.
• Coordinate scheduling of inlife activities with rest of the study team and supporting staff.
• Establish and maintain a comprehensive training program for inlife personnel.
• Ensure that team members are appropriately trained and qualified to perform assigned procedures and study activities.
• Identify training gaps and develop plans to enhance technical competency, operational flexibility, and cross-training.
• Identify opportunities to improve operational efficiency, productivity, and resource utilization.
• Develop and implement standardized workflows, scheduling practices, and operational procedures.
• Ensure that all inlife activities are conducted in accordance with approved study protocols, SOPs, GLP requirements, and applicable regulatory guidelines.
• Promote a strong quality culture and ensure timely documentation of study activities.

Qualifications and Experience:

• Bachelor's degree in Animal Science, Biology, Toxicology, or a related scientific discipline; advanced degree preferred.
• 15+ years of experience in nonclinical toxicology or preclinical research, preferably within a GLP-regulated CRO environment.
• Minimum of 10 years of experience in a supervisory or management role overseeing inlife operations or related activities.
• Demonstrated experience managing personnel, coordinating multiple studies, and optimizing operational resources.
• Strong knowledge of GLP requirements, animal welfare regulations, and nonclinical toxicology study execution.
• Experience with complex inlife procedures, including dosing, clinical observations, sample collection, and study termination activities.
• Experience developing training programs, managing operational schedules, and implementing process improvements.
• Proven ability to lead teams, resolve operational challenges, and work effectively across departments.

Salary: $90,000-$130,000, based on experience.

• 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 .