To be a good fit for this role, you would have:

• At least an Associate degree in computer science, information technology/systems, software engineering or a related field.
• The ability to think creatively for novel solutions to day-to-day challenges.
• The ability to think ahead and implement measures to mitigate any potential risks.
• A roll-up-your-sleeves attitude to tackle issues if they arise.
• Flexibility to troubleshoot issues outside of fixed working hours if urgent unforeseen issues arise and flexibility to (occasionally) cover other US time zones on a rotational basis with other team members if needed.
• The ability to lead and work with others in a positive and collaborative manner to set and meet organizational goals.
• Exceptional attention to detail.
• Fully vaccinated and boosted status against COVID-19. (Vaccination is a requirement unless medical or religious accommodation is requested and approved.)

To be a good fit for this role, you would have:

• At least a diploma in accounting, finance or a related field.
• Working experience as a finance officer or in a related role is preferred. Fresh graduates with a strong motivation to learn are welcome.
• Exceptional attention to detail with a high degree of meticulousness.
• The ability to work efficiently and accurately to meet deadlines.
• A high level of professionalism and integrity in handling confidential information.
• Fully vaccinated and boosted status against COVID-19. (Vaccination is a requirement unless medical or religious accommodation is requested and approved.)

To be a good fit for this role, you would have:

• MD, PhD or the equivalent in a relevant field. Board certification in oncology or oncology subspecialty would be an advantage.
• Experience planning, designing and executing clinical trials in the molecular diagnostics or oncology therapeutics space.
• Experience interacting with public payers and relevant regulatory agencies to drive the development and subsequent approval of IVD (or therapeutic agent).
• An established professional network in the oncology community with KOLs, industry and regulatory personnel.
• Thorough understanding of good clinical practice (GCP), FDA and EMA regulations and ICH guidelines.
• Strong leadership skills and the ability to lead cross-functional teams across R&D, Software, Bioinformatics, Clinical Laboratory, Regulatory, Quality and Commercial to spearhead the company’s development pipeline.
• Excellent oral and written communication skills, with the ability to discuss scientific/technical data and regulatory requirements with key stakeholders both internally and externally.
• The ability to work collaboratively and independently as a self-motivated team player, and balance multiple priorities in a fast-paced culturally diverse start-up environment.
• Fully vaccinated status against COVID-19. (Vaccination is a requirement unless medical or religious accommodation is requested and approved.)

To be a good fit for this role, you would have:

• At least a Bachelor’s degree in Biological Sciences, Life Sciences or a relevant field.
• An active California Clinical Laboratory Scientist license (generalist/CGMBS) in good standing.
• At least 2 years of experience working in a regulated laboratory environment.
• Familiarity with molecular diagnostic techniques, especially next generation sequencing.
• Experience in liquid biopsy is advantageous.
• Familiarity with laboratory information management systems.
• Experience in setting up and using laboratory automation and associated programming would be highly advantageous.
• A high degree of attention to detail.
• Willingness to ‘roll your sleeves up’ and ability to work collaboratively with others.
• The ability to commit full-time to this role. Usual working hours would be 9am-6pm / 10am-7pm / 11am-8pm, subject to adjustments. Flexibility in working weekends would be a plus.
• Fully vaccinated status against COVID-19. (Vaccination is a requirement unless a medical or religious accommodation is requested and approved.)

To be a good fit for this role, you would have:

• At least an associate degree in an area relevant to the laboratory. Experience working in a clinical laboratory would be a plus.
• Flexibility in being rostered on weekends would be a plus. (Usual working hours would be 8am-5pm / 9am-6pm, subject to adjustments.)
• Exceptional attention to detail, being highly meticulous and organized. This is an administrative role that is a crucial part of our workflow.
• The ability to work with others in a positive and collaborative manner to meet organizational goals.
• Fully vaccinated status against COVID-19. (Vaccination is a requirement unless a medical or religious accommodation is requested and approved.)

To be a good fit for this role, you would have:

• A PhD in a relevant field Science or Engineering or Master’s with 3 years of relevant work experience.
• Relevant working experience with NGS assays and liquid handling robotics platforms.
• Strong technical understanding of genetic analysis tools, workflows, and chemistry in NGS assays.
• Experience working within regulated environments (e.g. IVD, LDT).
• Experience developing laboratory processes from conceptualization to process validation and implementation.
• Strong interpersonal and communication skills.
• A positive mindset and the ability to lead and work with others even when the going gets tough.
• Exceptional attention to detail in the monitoring of quality data and troubleshooting of issues.
• Excellent organizational skills, including the ability to efficiently evaluate, prioritize and handle multiple priorities and timelines.
• Fully vaccinated status against COVID-19. (Vaccination is a requirement unless medical or religious accommodation is requested and approved.)

To be a good fit for this role, you would have:

• At least a Bachelor’s degree in a relevant field of Science or Engineering.
• Relevant working experience with next generation sequencing (NGS) assays and liquid handling robotics platforms (requiredhighly preferred).
• Strong technical understanding of laboratory automation tools used and operation concepts in NGS.
• Experience working within regulated environments (e.g. IVD, LDT).
• Experience developing laboratory processes from conceptualization to process validation and implementation.
• Strong interpersonal and communication skills.
• A positive mindset and the ability to lead and work with others even when the going gets tough.
• Exceptional attention to detail in the monitoring of quality data and troubleshooting of issues.
• Fully vaccinated status against COVID-19. (Vaccination is a requirement unless medical or religious accommodation is requested and approved.)

To be a good fit for this role, you would have:

• An MD, PhD, PA-C, NP or RN with Clinical Oncology experience. Genetic counseling qualifications are a plus.
• 2 years’ experience as MSL/clinical science liaison (CSL) in Oncology preferred. Product launch and/or start-up experience is a plus.
• Experience working with experts at academic medical centers to build consensus around new products and/or services.
• Experience in establishing strong, collaborative working relationships with internal stakeholder functions (e.g. Sales, Marketing, Regulatory, R&D) and external customers.
• Excellent written and oral communication with strong interpersonal and organizational skills.
• Ability to understand and effectively communicate scientific and medical information to both internal and external stakeholders.
• Strong problem-solving skills, good attention to detail, time management skills and personal initiative.
• Positive can-do attitude with an ability and want to thrive in a start-up environment. This includes being able to embrace change and multi-task in a fast-paced environment.
• Ability to work both independently and collaboratively with the Field Commercial Team.
• Ability to travel to meet with KOLs, attend physician education talks and conferences (including specialty society scientific meetings) as required.
• Fully vaccinated status against COVID-19. (Vaccination is a requirement unless a medical or religious accommodation is requested and approved.)