Job Information
ICON Clinical Research Senior Research Associate in Portland, Oregon
Senior Research Associate- Portland, OR (onsite)
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 Associate- Portland, OR- on site
We are currently seeking an Senior Research Associate to join our diverse and dynamic team.
What you will be doing
Accurately follow detailed instructions for the production of biological reagents and kits as outlined in controlled documentation and manufacturing policies, procedures, and work instructions
Utilize existing production protocols to generate products within specifications
Provide peer review on Production related document revisions. Initiate such revisions as appropriate
Create and accurately maintain production-related documents and records for production and quality assurance
Monitor supplies of raw materials related to production activities, and report inventory needs to Production management, as appropriate
Perform material qualification and in-process laboratory tests as assigned
Assist research and development in the testing of new products as assigned
The SRA is responsible for adhering to Production protocols as well as all QMS related procedures.
Formulate, culture, evaluate, aliquot, label, package, and test specialty reagents for clinical lab use
Maintain supply and reagent inventory for the Production Department
Develop knowledge and experience with all clinical reagents and assays
Assist in document writing and tech transfer of new clinical test
Laboratory cleaning
Interactions with Enterprise systems as appropriate, including physical inventory support
Provide review of controlled documentation and Production records
Your profile
Proficient in use of standard lab equipment and Microsoft Office
PCR, NanoDrop, ddPCR, cell culture experience all highly beneficial/required
Minimum 3 years hands on/lab bench experience along with a bachelor’s degree
Demonstrated ability to closely follow written instructions and communicate clearly with others
Ability to take direction, and carry out instructions with little oversight; complete tasks accurately, reproducibly, and on time; and accurately document activity
Exceptional organization skills, attention to detail, and analytical ability
Effective communicator (orally, written, and formal presentations)
Ability to work well with others
Efficient, task driven work ethic, with an eye for process improvement
Ability to accept responsibility with accountability and integrity
Experience with GMP, ISO, IVD/IDE requirements a plus
#LI-FL1
#onsite
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.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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)
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply
ICON Clinical Research
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