Job details
Job type full-time
Full job description
For candidates in the uk this will be working monday to friday 12noon to 8pm to cover the us time zones.
Purpose
Experience in cell or gene therapies along with biomarkers is required
Provide scientific and technical advice to guide and make recommendations with key pharma customers for their oncology clinical development programsTo ensure these match with internal capabilities ensuring coordination with technical, scientific support and sales functions across the americas, europe, asia pacific and china labs.
The position would be based in asia, supporting both global and local clinical development programs.
Responsibilities
Main scientific point of contact and provides global scientific oversight for key customers.
Ensures early engagement between biomarker scientists and clinical scientists to provide input in tests, platforms and associated technical aspects of the trials.
Supports feasibility discussions concerning assay transfer and test validation to ensure biomarker methods fit the study requirements including new technology evaluation.
Coordinates scientific activities across q2 solutions lab network and scientific advisors (e.gOncology, anatomic pathology, genomics, immunoassays, flow cytometry and cdx/ivd, regulatory)
Responsible for scientific escalation
Contributes to the scientific governance meetings
Utilize the extended capabilities of our parent organizations, iqvia and quest diagnostics for disease area and other subject matter expertise
Provide scientific/technical support for bid defense prep meetings and capability presentations for oncology trials.
Support scientifically sound approach/proposal forward to bid team for requests for information (rfis), requests for proposals (rfps), and other queries related to oncology clinical trials.
Work with internal functions (e.gMarketing, strategy) to help create scientific client-facing material (e.gSlide decks, webinars, newsletters, web content, etc.) and represent q2 solutions at conferences and other events related to oncology clinical trials.
Utilize sound knowledge and understanding of q2 solutions internal processes, practices and capabilities.
Required knowledge, skills and abilities
Possess a general knowledge of clinical laboratory regulations, ich and gxp guidelines.
Possess effective communication skills, both written and verbal english.
Must be detail oriented with excellent organizational skills.
Must be open to travelling.
Minimum required education and experience
B.scDiploma is a minimal requirement.
A minimum of 5 years of experience in the pharmaceutical or clinical trial environment including experience with biomarkers.
Ph.dDiploma is an asset.
Q² solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutionsHttps://www.q2labsolutions.com/careers
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilitiesHttps://jobs.iqvia.com/q2-solutions-eoe
As the covid-19 virus continues to evolve, q² solutions` ability to operate and provide certain services to customers and partners necessitates q² solutions and its employees meet specific requirements regarding vaccination statusHttps://jobs.iqvia.com/q2-solutions-covid-19-vaccine-status
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Posted 30+ days ago
