Senior Research Scientist

ICON plc • Portland, OR

23h • Onsite

About The Position

Senior Research Scientist - Portland OR- on site ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development 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. 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

Requirements

• 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
• 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.
• 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
• 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

Responsibilities

• Oversee the scientific aspects of an assay development/validation project
• 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
• Attend and present results at client facing meetings
• Serve as a scientific leader within the department

Benefits

• 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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree