Job Overview The Bioanalyst supports bioanalytical operations within an early-phase clinical trial environment by combining quality oversight responsibilities with hands-on laboratory support. This role focuses on ensuring GxP compliance, data integrity, and operational excellence through inventory and asset management, documentation review, study plan and report preparation, and quality review of laboratory data. The Bioanalyst collaborates closely with scientists and project teams to drive study timelines, coordinate laboratory activities, and support equipment qualification, software validation, and biospecimen processing. This position is ideal for a laboratory generalist looking to specialize in bioanalytical quality and operations while contributing to high-quality clinical research outcomes. Requirements 2-4 years of laboratory experience, preferably in a regulated (GxP) environment. Strong understanding of laboratory operations, quality oversight, and data integrity principles. Excellent analytical, organizational, and time management skills with the ability to manage multiple priorities. Experience with laboratory documentation, regulatory compliance, equipment qualification, and biospecimen handling.

Job Types:

Full-time, Contract Pay:

$20.00 - $22.00 per hour Expected hours: 40.0 per week

Benefits:

401(k) Dental insurance Health insurance Vision insurance Application Question(s): Are you available for a day-shift opportunity? (Full-Time) Are you comfortable working on a 12-month contract? (Potential extensions) How far do you live from the address?

Education:

High school or equivalent (Required)

Experience:

Laboratory:

2 years (Required) Ability to

Commute:

New Haven, CT 06511 (Required)

Work Location:

In person