Senior Research Scientist

ICON Clinical Research; Portland (OR); On-site; USD 110,000 - 160,000; Full time

Job summary

ICON Clinical Research is seeking a Senior Research Scientist for an on-site role in Portland, OR. You will oversee the scientific aspects of assay development and validation, with preference for experience in medical device design/manufacturing following ISO 13485 standards.

The role requires rigorous project management and ability to lead cross-functional teams in a fast-paced environment. The successful candidate will direct development and validation of genomic assays, present at client

Qualifications

• Minimum 6 years of experience in genomic assays.
• PhD preferred; or a Bachelor's/Master's with 6–8 years experience.
• Experience with medical device design/manufacturing or ISO 13485 is preferred.
• Strong interpersonal and communication skills; able to work independently and efficiently.

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, cross-functional interactions.
• Attend and present results at client meetings.
• Maintain high quality and meet deadlines across multiple projects.
• Provide scientific leadership within the department.

Skills

Genomic assays

Scientific leadership

RT-PCR/qPCR/ddPCR

Communication

Project management

Education

PhD in science related field

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

Job description

Senior Research Scientist- onsite- Portland OR

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Senior Research Scientist

This is an On-Site role located in Portland, OR

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. The primary role of the Senior Research Scientist is to oversee the scientific aspects of an assay development/validation project. Experience with medical device design manufacturing following ISO 13485 standards preferred.

• Independently direct development and validation of new genomic assays
• Exhibit scientific leadership related to the testing of clinical trial samples for RT-PCR, qPCR, and ddPCR assays
• Independently manage all aspects of R&D assay validations; experiments, data analysis, sponsor updates, interact with: Scientific Affairs, IT, operational labs, business development, and project management teams
• Experienced multi-tasker with the ability to work independently with a high degree of quality
• Attend and present results at client facing meetings
• Excellent oral and written communication skills
• Proven track record in delivering focused customer service and client satisfaction
• Experience in managing multiple projects and meeting deadlines
• Excellent presentation skills
• Serve as a scientific leader within the department
• Ability to remain composed and even keeled in stressful situations, performing effectively in spite of shifting priorities, workload and external pressures
• Knowledge of basic computer programs

To be successful in this role, you will have:

• Minimum 6 years of experience in genomic assays
• PhD in science related field preferred, Bachelors or master's with 6 to 8 years of experience
• Experience with medical device design or manufacturing following ISO 13485 standards preferred.
• Strong interpersonal and communication skills, good laboratory, and organizational skills, including the ability to work independently and efficiently.
• Ability to multitask, along with an orientation toward teamwork and leadership, and strong creative thinking and problem-solving skills.

#LI-FL-1

What ICON can offer you:

Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)