Clinical Pathology Sample Technician

Davita Inc.; Evansville (IN); On-site; USD 38,000 - 46,000; Full time

Job summary

A leading company in drug discovery is seeking an organized individual for a role in clinical sample processing. This position involves managing shipments, processing specimens, and ensuring compliance with regulations. The ideal candidate will have strong attention to detail, excellent organizational skills, and the ability to manage multiple studies effectively. Join our team to make a meaningful impact in advancing research and science.

Benefits

Health and dental coverage

Disability insurance

Paid time off

Parental leave

401K

Qualifications

• Ability to read, write, and understand English.
• Frequent lifting of over 50 lbs required.
• Willingness to wear PPE as required.

Responsibilities

• Manage all shipments for clinical pathology and assist in specimen processing.
• Prepare and maintain schedules for sample shipments using internal systems.
• Review and ensure compliance with established protocols and regulations.

Skills

Attention to detail

Organizational skills

Ability to understand instructions

Communication skills

Tools

Windows software applications

Job description

We are seeking an organized and detail-oriented individual to join our clinical sample processing team. This role involves managing all shipments for clinical pathology and assisting in specimen processing.

Work Schedule and Compensation

Monday - Friday, 6am - 4pm
Starts at $19/hour + full benefits within 30 days of hire
Eligible for overtime

Responsibilities

• Review study protocols and ensure tasks and data for pre-clinical research are conducted according to established protocols, SOPs, GLPs, and regulatory requirements.
• Generate study forms and worksheets independently.
• Prepare and maintain schedules for study sample shipments using internal electronic systems.
• Prepare shipments of study samples in compliance with local and federal regulations.
• Notify recipients promptly with tracking information, sample inventory sheets, and electronic manifests.
• Label samples using automated and manual systems, and label cups and tubes for studies.
• Ensure adequate inventory of supplies for sample collection.
• Review sample labels and specimens for accuracy and quality standards.
• Operate centrifuge for collected samples according to SOP and protocol requirements; store serum/plasma appropriately.
• Maintain proper storage conditions for different sample types.
• Process specimens accurately within established metrics.
• Maintain equipment and instrumentation.
• Notify the Study Director of sample quality issues and document appropriately.
• Manage multiple studies, learn protocol review, and attend PI meetings.
• Document activities and record observations in accordance with GLPs, SOPs, and protocols.
• Plan workload effectively to complete multiple assignments.
• Produce high-quality data under strict deadlines.
• Recognize deviations, determine actions, notify supervisors, and document issues.
• Review data to identify potential problems.
• Prepare and ship numerous samples daily.

Performance Requirements

Characteristics described are typical of those encountered in this role. Reasonable accommodations may be provided for individuals with disabilities.

General

• Ability to read, write, speak, and understand English.
• Ability to understand written and oral instructions.

Physical Activity

• Frequent walking, sitting, carrying, standing, heavy lifting (min 50 lbs.), reaching, gripping, twisting, and repetitive motions.
• Ability to walk over rough terrain.

Working Conditions

• Exposure to hazardous chemicals, biological materials, and mechanical hazards; immunizations may be required.
• Negative Mantoux TB test or chest X-ray required.
• Ability to wear PPE as needed.
• Potential exposure to animal dander/materials.
• Moderate noise level.

Tools and Resources

• Use of various software applications on a Windows platform (Excel, Word, PowerPoint, etc.).

This position may be offered at different levels depending on education and experience, with salary adjusted accordingly.

#LI-Onsite #LI-OF1

About Inotiv

Inotiv is a growing drug discovery and development company committed to impacting health and well-being worldwide. We offer career opportunities for individuals with the talent and desire to make a difference. Join us in advancing research and science to improve lives.

Salary is commensurate with experience. Benefits include health and dental coverage, disability insurance, paid time off, parental leave, 401K, and more.

Inotiv is an Equal Opportunity Employer, providing fair employment opportunities regardless of age, race, color, religion, sex, gender identity, sexual orientation, disability, or other protected status.