At a Glance
- Tasks: Support clinical evidence generation and collaborate on oncology diagnostics projects.
- Company: Join a leading medical diagnostics organisation with a focus on innovation.
- Benefits: Competitive salary, remote work options, and comprehensive benefits package.
- Other info: Inclusive workplace culture with opportunities for professional growth.
- Why this job: Make a real impact in the field of oncology and advance your career in clinical science.
- Qualifications: 4+ years in clinical research or IVD product development; strong scientific writing skills.
Job DescriptionWe are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer (OCMO) Global Clinical Affairs team. The CAS' main responsibilities will be to support clinical evidence generation, in conjunction with cross-functional teams as part of the co-development process of companion diagnostics in the field of oncology. This position will support clinical trial study designs and execution, regulatory applications, and scientific marketing deliverables. The ideal candidate will have a strong background in clinical science/research and experience working in pharmaceutical, biomarker, and/or in vitro diagnostic clinical development. The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and external requirements. This position reports to the Manager of Clinical Affairs Sciences and has no direct reports. Generation of content to support external validation studies including study design and authoring of study protocols and reports. Design and develop databases, Electronic Data Capture (EDC) systems, and case report forms. Contribute to risk analyses, study quality control activities, and instream data monitoring in clinical trials. Ensure scientific validity of reported results including statistical analysis, tabulation, and presentation of data. Collaborate with regulatory and development teams during the submission process including authoring of clinical performance information and other documentation such as Instructions for Use (IFU).Provide clinical and scientific oversight of local marketing and commercial materials. Serve as the clinical science subject matter expert in cross-functional internal meetings as well as meetings with pharmaceutical partners and regulatory bodies. Support audits and inspections as a clinical subject matter expert. in pharmaceutical, medical or relevant biomedical science fields. 4+ years of experience in IVD product development, clinical research, medical writing, and/or clinical science in the medical device and/or pharmaceutical industry. Ability to interpret regulatory standards, guidance, and laws. Strong scientific, medical writing, and presentation skillsExceptional ability to manage multiple projects in a fast-paced environment with changing priorities. Must be able to work and make independent decisions, understand complex scientific and clinical data information, and be able to take the initiative to lead projects and assignments. Experience working with external partners and/or regulatory bodies including the FDA.Knowledge in oncology, immunology, and/or pathology preferred. Additional DetailsThis job has a full time weekly schedule. It includes the option to work remotely. The full-time equivalent pay range for this position is $105,280.00 - $197,400.00/yr plus eligibility for bonus, stock and benefits. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.For more information about equal employment opportunity protections, please visit Required: NoShift: DayDuration: No End DateJob Function: Medical/ClinicalSummaryLocation: US-CA-Carpinteria; US-NY-Remote Location; US-NJ-Remote Location; US-NH-Remote Location; US-DC-Remote Location; US-NC-Remote Location; US-PA-Remote Location-Philadelphia Area; US-MD-Remote Location; US-VA-Remote Location; US-TX-Remote Location; US-RI-Remote Location; US-IN-Remote Location; US-IL-Remote Location-Wood Dale Area; US-NC-Remote Location-Durham Area; US-MA-Remote Location-Lexington Area; US-IL-Remote Location; US-GA-Remote Location; US-DE-Remote Location; US-FL-Remote Location; US-DE-Remote Location-Wilmington/Newport Area; US-CA-Remote Location; US-MA-Remote Location-Boston City Limits; US-NY-Remote Location-Manhattan City Limits; US-MA-Remote Location; US-VA-Remote Location-Reston Area; US-TX-Remote Location-Houston Area; US-CT-Remote LocationType: Full time
Clinical Scientist - Genetics employer: Agilent Technologies
Agilent is an exceptional employer that fosters a culture of innovation and collaboration, making it an ideal place for sales professionals in the scientific field. With a commitment to employee growth, competitive compensation, and a supportive work environment, Agilent empowers its team members to excel in their careers while contributing to meaningful advancements in life sciences. Located in the UK South and Midlands, this role offers the unique opportunity to engage with diverse sectors, ensuring that employees can make a significant impact in their communities.
