Research Associate II, Translational Biology & Sample Mgmt

Actalent; Columbus (OH); On-site; USD 39,000 - 47,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

Time Off/Leave

Job summary

Actalent in Columbus, OH is seeking Research Associate I and II to join a fast-paced biologics and gene therapy environment. The roles focus on clinical sample management, documentation, and support for translational biology programs in a GCP/GLP setting.

You will collaborate with Clinical Operations, Data Management, and external partners to track samples, manage biospecimens, maintain databases, and ensure compliance across studies.

Qualifications

• Experience in clinical sample management within a biotech/healthcare setting.
• Familiarity with GCP/GLP environments and regulatory standards.
• Strong written and verbal communication for cross-functional collaboration.

Responsibilities

• Support translational biology efforts for RNA, siRNA, gene therapy, and genome editing.
• Organize and maintain clinical sample documentation across studies.
• Develop and implement a centralized database for samples and consent tracking.
• Ensure adherence to GCP/GLP guidelines and quality standards.
• Collaborate with Clinical Operations, Data Management, Biostatistics, and CROs.

Skills

Clinical sample management

GCP/GLP compliance

Documentation & data entry

Cross-functional teamwork

Scientific writing

Education

B.S. in Biology or related field

Job description

Actalent in Columbus, OH is seeking Research Associate I and II to join a fast-paced biologics and gene therapy environment. The roles focus on clinical sample management, documentation, and support for translational biology programs in a GCP/GLP setting.

You will collaborate with Clinical Operations, Data Management, and external partners to track samples, manage biospecimens, maintain databases, and ensure compliance across studies.