Associate Director Companion Diagnostics Project Manager

Posted 9 days 8 hours ago by Daiichi Sankyo, Inc.

Permanent
Full Time
Science & Technology
New Jersey, Basking Ridge, United States, 07920
Job Description

Job Summary:

The Associate Director, Companion Diagnostics Project Manager will be responsible for ensuring that objectives of projects are set in alignment with the therapeutic and diagnostic team needs, are implemented and are accomplished within the defined time-frame and budget. The CDx Project Manager will in partnership with the CDx Leader serve as the main facilitator of interactions between the external Diagnostic Partners and the internal Daiichi Sankyo stakeholders.

Responsibilities:
Creating and executing enterprise wide CDx project work plans with Diagnostic partner and internal teams, and modifying as appropriate to meet changing needs and requirements
Tracking project scope, costs, expenses, budgets against defined metrics in active alignment with CDx lead and key functional stakeholders
Providing complete tracking of all project phases and activities - communication of timelines, milestones and goals to project team and department leadership
Ensuring that project documents are complete, current, and available to team in a centralized location
Participating in preparation of slides and alignment of communications and decision processes in partnership with CDx Lead
Communicating issues and minimizing risks as well as creating associated mitigation strategies for all ongoing CDx projects
Organizing and facilitating global CDx team meetings and interactions with Dx partner
Qualifications
Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation.

Education/Experience:
Qualified candidates must have a Bachelor's degree from an accredited college or university; Candidate will have a degree in biological sciences or a related discipline. A BS or MS degree, or PhD.
Experience in Companion Diagnostics strongly preferred.
Completion of Project Management Training is a plus.
Minimum 7 years (w/BS), 5+ years (w/MS), 3+ (w/PhD) relevant experience in pharmaceutical/diagnostics setting and managing complex development projects
Demonstrated track record of success working on a multidisciplinary pharma/diagnostic development team.
Knowledge of design control, market and product requirements management, and the IVD development process is a plus.
Knowledge of molecular diagnostics technology, competitors, and market space is preferred.
Established expertise and hands-on experience with Microsoft Project, Word, Excel, PowerPoint, Outlook, Sharepoint and remote meeting tools such as WebEx, Live Meeting
Expert planning and tracking skills, with the ability to capture details and summarize in an integrated cross-functional plan
Well- organized, focused on results, capable of managing multiple projects, excellent time management skills.
Ability to work in a highly collaborative environment globally with stakeholders from multiple functional areas
Solid interpersonal and verbal and written communication skills

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