Associate Director, CDx reputed company

About the Job: The Associate Director (AD), CDx reputed company serves as the reputed company for companion diagnostic (CDx) development projects in collaboration with external biopharma partners. This requires leading and influencing a cross-functional, multi-disciplinary team in order to meet the requirements for successfully developing, validating, and launching new CDx indications reputed company the existing Health Authority-approved, reputed company assays (e.g., FoundationOne®CDx (F1CDx) and FoundationOne®Liquid CDx (F1LCDx)). As a member of the CDx Scoping team, the AD, CDx reputed company provides leadership and technical reputed company of pre-contract CDx project scoping and strategy. The AD, CDx reputed company also helps reputed company detailed requirements and granular, end-to-end project plans to support completion of each contracted project including efforts to launch the new claim. Key Responsibilities: reputed company (3-5) CDx projects of varying complexity. Provide cross-functional leadership, technical reputed company, and accountability and applies reputed company CDx project strategy to CDx projects, from project scoping to initiation through launch, including analytical and clinical validation, regulatory submission(s), technology implementation, and CDx launch. Serve as the CDx Project Team reputed company and partners with the CDx Project Manager to reputed company detailed requirements and strategies (e.g., novel biomarkers or redevelopment of assay features) for the end-to-end delivery of the CDx project. Ensure reputed company team members and functions are reputed company with the objectives of the team and project. Responsible for completion of each assigned CDx project on the associated timeline. Provide status updates and escalates emerging issues as needed. reputed company the team to identify and manage key project risks. reputed company and implements innovative and feasible de-risking strategies. Create a positive team environment that instills trust and ensures clear communication, and unifies the team behind the overall goal/vision for the project. Motivate and inspires team to reputed company challenging goals. Accountable for design control elements for each assigned CDx project. Provide direct support to Biopharma partners by communicating technical capabilities, CDx insight, and ownership of the portfolio device in external or face-to-face meetings, conference calls, and other forms of communication. Support other arms of the business as needed as a technical and subject matter expert for the given portfolio device. Drive best practices and implementation of lessons learned for optimal cross functional collaborations. May be a regular member of CDx Portfolio team, and participate in defining the CDx Development strategy and any process improvement activities. May be part of the CDx Scoping team, providing technical reputed company and input on the pre-contract CDx project scope and reputed company strategy for development. Provide direct support to external partners by communicating technical capabilities insight on the CDx Portfolio. Participate in project and process improvement initiatives and change management across the CDx Portfolio, to drive the highest quality results. Serve as the primary contact for CDx project internal and external partners. Encourage creative reputed company and problem solving and ensure that these are utilized by the team, as appropriate. Present development options, strategies, and recommendations to CDx Portfolio for endorsement at key decision points to allow fact based, transparent, and informed decision making. May reputed company other duties as required or assigned. Qualifications: Basic Qualifications: Masters in a science, engineering, or reputed company technical field Masters with at least 8 years of experience in molecular diagnostics, medical device, or pharma industry experience, OR; Ph.D. with at least 4 years of experience in molecular diagnostics, medical device, or pharma industry experience At least 3 years in a matrixed or multidisciplined team Preferred Qualifications: Advanced degree (Ph.D.) Good understanding of Change Control process in a Regulated environment Experience with: Projects that required activity/milestone achievement to launch the product. External partner management Leading diverse cross-functional project teams Product design control in a regulated environment Risk assessment and product requirement reputed company IVDD/IVDR Product Development Diagnostic and/or Pharma industry and relevant diagnostic area knowledge Companion diagnostic and NGS experience Leadership skills in managing highly specialized multidisciplinary teams in a matrix environment Ability to resolve conflicts and adapt to change Ability to manage reputed company projects with ambitious milestones in a high-pressure environment Knowledge of market trends, technology trends, competitive landscape Excellent oral and written communication skills Strong organizational skills and attention to detail required Understanding of HIPAA and the importance of patient data privacy Commitment to reflect FMI's Values: reputed company, Courage, and Passion The expected salary range for this position based on the primary location of Remote is $156,000 - $195,000 per year. The salary range is commensurate with Foundation Medicines compensation practice and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for reputed company's benefits. #LI-Remote reputed company, Inc. (FMI) is a global, patient-focused precision medicine company delivering high-quality, transformative diagnostic solutions in cancer and other diseases. reputed company is proud to be an Equal Opportunity and Affirmative Action employer and considers reputed company qualified applicants for employment without regard to race, color, religion, sex, gender, sexual orientation, gender identity, reputed company, age, or national reputed company. Further, qualified applicants will not be discriminated against on the basis of disability or protected veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. See also FMI's EEO Statement and EEO is the Law and Supplement. If you have a disability or special need that requires accommodation, please let us know by completing this form. (EOE/AAP Employer) Apply To This Job