Research Associate I, Sample Processing

About the role

Supervises and coordinates all study-related activities of research technical staff to ensure compliance with the protocol and applicable SOPs and maintains the raw data for nonclinical studies.

Responsibilities

• Coordinates assignments to facilitate scheduling of study-related events on assigned studies (in conjunction with other departments) to ensure protocol requirements are met.
• May perform peer reviews and QC as needed.
• Responsible for the accurate preparation and review of study calendars from draft and final protocols and ensuring all protocol-driven activities are accurately scheduled.
• Monitors scientific projects, and the conduct of procedures in accordance with the study protocol, and applicable SOPs.
• Acts as liaison between technical staff, internal departments, and Study Director on assigned studies.
• Responsible for the preparation of study notebooks, organization of study data, and timely review of all study-related data generated by SPL (according to established metrics).
• May perform limited technical activities as needed.
• Participate in the team meetings.
• Coordinate ordering of study equipment and supplies.
• Perform all other related duties as assigned.

Qualifications

• Education: High school diploma or General Education Degree (G.E.D.) preferred.
• Experience: 2 years of related experience in a GLP environment. Experience with research and investigation procedures, techniques, and literature.
• An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
• Certification/Licensure: None, unless required by local government.
• Other: Ability to organize, prioritize work and meet deadlines. Computer literacy with word processing, spreadsheet, and data base programs. Must be authorized to work in United States without a sponsor visa now or in the future.

Requirements

Physical Demands: