{"id":4210374,"url":"https://alion.io/job/grail-associate-scientist-2-assay-rd","title":"Associate Scientist 2 - Assay R&D","company":{"id":3593,"name":"GRAIL","domain":"grail.com","url":"https://alion.io/company/grail","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Lever","truth_index":null},"role":"Science & Research","role_family":"Science & Research","seniority":"junior","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Durham, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"21 CFR Part 11","optional":false},{"name":"GMP","optional":false},{"name":"ISO 13485","optional":false},{"name":"IVDR","optional":false}],"status":"live","first_seen_at":"2026-11-12T18:29:36Z","employer_posted_date":"2026-11-12","last_verified_at":"2026-11-13T00:49:57Z","board_verified":true,"closed_at":null,"days_open":0,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":0},"description":"The Associate Scientist 2 is a developing professional role that applies growing scientific expertise to independently execute standard laboratory procedures and contribute to more complex research activities. This position performs molecular biology, protein expression, purification, and related analytical techniques with increasing autonomy, ensuring accuracy, compliance, and high-quality documentation. The Associate Scientist 2 advances research objectives by applying professional judgment within established scientific and operational frameworks, supporting data interpretation, and contributing to the overall effectiveness of the laboratory environment.\nThis role is based in Durham, North Carolina, and requires full-time on-site attendance at GRAIL's Research Triangle Park (RTP) laboratory (4001 E NC 54 HW Assembly Suite 1100, Durham, NC 27709).\nResponsibilities:\nPerform a range of established laboratory experiments using professional methods in molecular biology, including RNA isolation, genomic DNA isolation, cDNA preparation, cloning, fermentation, protein expression, and purification with increasing independence and accuracy.\nPrepare, process, and analyze samples, reagents, buffers, and media for experimental workflows while applying professional judgment to ensure precision, proper documentation, and procedural compliance.\nCollect, interpret, and document experimental data in laboratory notebooks or electronic systems using professional data management practices that support reproducibility and scientific integrity.\nOperate, maintain, and perform routine troubleshooting on laboratory equipment, identifying issues that require escalation and ensuring continuous readiness of instruments used in scientific work.\nAssist in refining laboratory protocols or methods by providing professional observations on workflow efficiency, data quality, and opportunities for procedural improvement.\nContribute to the preparation of technical reports, data summaries, protocol drafts, and quantitative analyses to support scientific communication and project decision-making.\nEnsure adherence to safety, regulatory, and quality standards in the handling of chemical and biological materials, demonstrating accountability for maintaining a professional laboratory environment.\nSupport laboratory operations through inventory oversight, organization of materials, coordination of supply needs, and contributions to continuous process improvements.\nProvide informal guidance and technical support to junior laboratory staff by sharing professional knowledge, reinforcing documentation standards, and modeling effective laboratory practices.\nThese job duties are a summary of the primary duties and responsibilities of the job and position. It is not intended to be a comprehensive or all-inclusive listing of duties and responsibilities. Contents are subject to change at the company's discretion. \nAdaptability and Growth Expectation:\nAs our organization continues to evolve and grow, this role may require flexibility in responsibilities and duties. Employees should expect that their role may expand, shift, or be modified to meet changing business needs, strategic priorities, and organizational objectives.\nThis may include:\nTaking on additional responsibilities.\nParticipating in cross functional projects and initiatives. \nAdapting to new technologies, processes, or methodologies.\nSupporting other departments or teams during periods of high demand.\nContributing to special projects or temporary assignments as needed.\nRequired Qualifications:\nBachelor’s degree in Biology, Chemistry, Biochemistry, or related scientific discipline with 2-5 years of relevant experience; OR Master’s degree in a related field with 0-2 years of relevant experience.\nDemonstrated level of knowledge regarding applicable regulatory standards commensurate with the position's complexity and scope, contributing to organizational regulatory compliance. Minimal applicable standards for this position include:\nGMP quality management systems (e.g. ISO 13485)\nOperations within the regulated medical device environment (e.g. IVDD, IVDR, FDA 21 CFR 800 series, FDA 21 CFR Part 11)\nPreferred Qualifications:\nSolid technical proficiency in standard laboratory techniques and equipment operation.\nAbility to analyze data, identify issues, and communicate findings clearly.\nStrong organizational and problem-solving skills with attention to detail.\nEffective communication skills, both written and verbal.\nAbility to work both independently and collaboratively within a team environment.\nFamiliarity with laboratory documentation systems, data management tools, and reporting processes.\nKnowledge of laboratory safety practices, compliance requirements, and quality standards.\nPhysical Demands and Environment:\nWork is primarily performed in a laboratory environment with exposure to biological, chemical, or hazardous materials.\nRoutine use of PPE including lab coats, gloves, and safety glasses is required.\nInvolves prolonged periods of standing, pipetting, and handling laboratory materials.\nMay occasionally require evening or weekend work to meet project demands.\nOperates under moderate supervision with periodic review of work products and outcomes.","description_format":"text","description_chars":5253,"description_truncated":false,"requirements":{"experience_years_min":2,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Diagnostic Tests & IVD","Molecular Diagnostics","Precision Medicine"],"lifecycle":[{"event":"open","at":"2026-11-13T00:49:57Z"}],"visa":[{"country":"US","licensed_sponsor":true,"adverts_offering_sponsorship_24m":0,"sanctioned_now":false,"evidence":"H-1B filings in 12 months: 15 · green card 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