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.)

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

• At least a bachelor’s degree in Biomedical Science, Life Sciences or its equivalent.
• Familiarity with molecular diagnostics techniques, including handling of patient samples, nucleic acid extraction, real-time PCR, genotyping and sequencing etc. would be an advantage
• Willingness to prepare for certification exams, such as for MT(ASCP) certification and California Clinical Laboratory Scientist license.
• Usual working hours would be 9 am-6 pm / 10 am-7 pm / 11 am-8 pm, and half-days on Sat, subject to adjustments. Flexibility in working on weekends would be a plus.
• A high degree of attention to detail and ability to stay focused executing complex laboratory protocols.
• Willingness to ‘roll your sleeves up’ and a ‘can-do’ attitude.
• Strong interpersonal and communication skills, ability to work collaboratively with others.
• Exceptional attention to detail as meticulousness is key when dealing with patient samples.
• Strong self-motivation, resilience, keen interest in learning and the ability to work well under pressure.
• Ability to work independently and complete assigned tasks in a timely manner.
• Fully vaccinated status against COVID-19.
• Willingness to be deployed overseas (USA) for a 1.5-year period upon completion of training (1-year period).

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

• PhD in Molecular Biology, Cancer Biology, Genomics or related field.
• At least 2 years of working experience in the research and development of molecular assays (we may also consider achievements and publications from your PhD course where relevant).
• Strong background in molecular biology knowledge, such as in PCR, RT-PCR, genotyping and NGS.
• Working experience in NGS data analysis. Some experience in developing bioinformatics algorithms independently.
• Proficiency in R or Python.
• The ability to work independently as well as in a team.
• Excellent communication and presentation skills and an ability to write summary reports.
• Strong self-motivation, resilience, adaptability and a keen interest in learning.
• Fully vaccinated status against COVID-19.

The following would be advantageous, but not required:

• Knowledge in genomic medicine and liquid biopsy.
• Experience in validation of NGS assays in a CLIA-compliant manner.
• Fluency in variant annotation and interpretation and use of genome databases such as COSMIC, ClinVar, Varsome, Ensembl and OncoKB.
• Ability to interpret genomic data in patient- and treatment-specific contexts following established procedures.
• Good track record of publications.

Specific title and responsibilities may be calibrated to match a given candidate’s experience.