Preclinical Study Director — GLP/Non-GLP Client Lead

NAMSA; Northwood (IA); On-site; USD 52,000 - 68,000; Full time

Job summary

NAMSA is seeking an Associate to support GLP and non-GLP preclinical studies in our Iowa facility. You will coordinate study conduct, communicate with clients, and help ensure quality system compliance.

Qualifications include a Bachelor's in science (two years of lab experience); a Master’s or PhD with relevant lab experience is also acceptable. Join NAMSA to advance in MedTech development and patient safety.

Qualifications

• Requires a minimum of a Bachelor’s degree, preferably in a scientific discipline, with a minimum of two years’ related laboratory experience.
• Master’s degree/PhD with a minimum of one year of relevant laboratory experience.

Responsibilities

• Assists in the coordination of study conduct tasks from study initiation to study completion.
• Performs noncomplex studies and serves as the primary contact for the client, as assigned, and keeps the client informed of schedule and any unforeseen events or issues.
• Performs project in compliance with applicable quality system regulations (i.e. ISO, GMP, GLP) and NAMSA SOPs.
• Serves as the Study Director for GLP and non-GLP preclinical studies and assures that all applicable GLP regulations are followed.
• Establishes and ensures schedule, budget and quality commitments are met for the client.

Education

Bachelor’s degree in a scientific discipline

Master’s degree/PhD with a minimum of one year of relevant laboratory experience

Job description

NAMSA is seeking an Associate to support GLP and non-GLP preclinical studies in our Iowa facility. You will coordinate study conduct, communicate with clients, and help ensure quality system compliance.

Qualifications include a Bachelor's in science (two years of lab experience); a Master’s or PhD with relevant lab experience is also acceptable. Join NAMSA to advance in MedTech development and patient safety.