Lead Genomic Assay Scientist - Portland (Onsite)

ICON Clinical Research; Portland (OR); On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

Annual leave entitlements

Health insurance for you and family

Retirement planning options

Global Employee Assistance Programme (

Life assurance

Country-specific optional benefits (e2

Gym memberships and travel discounts

Job summary

ICON Clinical Research in Portland, OR, is seeking a Senior Research Scientist for an on-site role. You will oversee genomic assay development and validation, lead testing of clinical trial samples (RT-PCR, qPCR, ddPCR), and manage multiple R&D projects while interfacing with Scientific Affairs, IT, lab operations, and clients.

The role requires strong scientific leadership, exceptional communication, and the ability to deliver high-quality results in a fast-paced environment.

Qualifications

• Minimum 6 years of experience in genomic assays.
• PhD preferred; Bachelor’s or Master’s with 6–8 years experience.
• Experience with medical device design/manufacturing following ISO 13485 standards preferred.
• Strong interpersonal and communication skills; ability to work independently.
• Multitask and leadership oriented; ability to manage multiple projects.

Responsibilities

• Independently direct development and validation of new genomic assays.
• Lead testing of clinical trial samples for RT-PCR, qPCR, and ddPCR assays.
• Manage all aspects of R&D assay validations; experiments, data analysis, sponsor updates, interact with Scientific Affairs, IT, labs, BD and project management teams.
• Attend and present results at client meetings.
• Serve as a scientific leader within the department.

Skills

Genomic assays experience

Communication skills

Leadership

Project management

Education

PhD in science related field

Bachelor’s or Master’s with 6–8 years experience

Tools

ISO 13485 familiarity

Job description

ICON Clinical Research in Portland, OR, is seeking a Senior Research Scientist for an on-site role. You will oversee genomic assay development and validation, lead testing of clinical trial samples (RT-PCR, qPCR, ddPCR), and manage multiple R&D projects while interfacing with Scientific Affairs, IT, lab operations, and clients.

The role requires strong scientific leadership, exceptional communication, and the ability to deliver high-quality results in a fast-paced environment.