Job Details

Payrate: $68.00 - $70.00/hr.

Summary:
In this vital role within the Precision Medicine Unit, the Precision Medicine Program Manager (PM) works closely with the Precision Medicine Lead (PML) to advance the development and execution of Precision Medicine plans. You will serve as the steward of a cross-functional team to develop and execute translational and precision medicine strategies to support asset (and above-asset, as needed) development across the product lifecycle. Additionally, you will partner with cross-functional Sr. Stakeholders and teams across Research & Development to guide the development of translational, reverse translational, and precision medicine strategies.

Responsibilities:

• Serve as the main steward of the PMed Team (PMT) overall program timelines, study pull-through and team efficiency by Driving the strategic planning, development and ensures execution of high quality, integrated cross-functional PMed Plans in support of the overall asset strategy & value
• Apply PM best practices in the planning, development, initiation, execution, QA/QC, and closing of projects while driving trade-off / decision making to ensure flawless execution
• Co-lead with PML content creation in preparation for cross-functional meetings, such as technical reviews (PMAF), Portal Reviews, Governance, etc.
• Conduct critical path analysis (challenging assumptions, hold cross-functional team members accountable); recognize and communicate inflection points w/ mitigation strategies
• Serve as an integrator to the Evidence Generation Teams (EGTs) and Product Teams (PTs) while ensuring connectivity with (inputs to/from) Discovery Bx, platform functions and IVD/Dx activities
• Drive risk management and effective communication plans, to include asset-wide impacts
• Ensure on time delivery; drive adherence to plan (time, budget and scope); challenge delays with ewhy notf and propose mitigations; quickly escalate changes to plan
• Internal Use Only General and Administrative
• Applying best practice project management methodology aligned with fs global commercialization process
• Ability to lead Agile teams and pivot quickly with changes in scientific or strategic assumptions based on internal / external data impacting the program
• Meeting effectiveness, MS Teams/Smartsheet maintenance, proper and timely escalation of issues to PMed TAHs
• What we expect from you
• We are all different, yet we all use our unique contributions to serve patients. The PMed Program Manager professional we seek is experienced, professional, dynamic, goal-oriented and results-driven with these

Basic Qualifications:

• PhD and/or master's degree and 2 years of relevant PM experience OR
• Bachelor's degree and 4 years of relevant PM experience OR
• Associates degree and 6 years of relevant PM experience

Preferred Qualifications:

• Technical / scientific background with 6+ years of industry and/or academic experience
• Prior pharma / consulting and/or drug development experience including deep experience in one or more core drug development and commercialization functions and experience leading teams through governance processes
• Development experience ideally incl. a program that involved one or more of the following: Research, early or late development; Diagnostics; Client biomarkers; Computational Biology; RWE
• Program and project management skills with experience in a healthcare-related environment, operationalizing strategic initiatives, including cross-functional strategic planning, development of integrated plans, monitoring and driving execution to plan
• Emotional intelligence skills include influencing without authority and navigating within a matrix environment.
• Experience using Project Management and AI/ML tools, methodologies, practices and infrastructure, as related to the Biopharmaceutical Industry
• Highly experienced on MS Suite tools (PowerPoint, Excel, etc.) and project management software such as Smartsheet, Planisware, SharePoint, etc.
• Finance and budget management experience
• Business process and systems management, Project planning and management (PMP preferred)
• Knowledge of SOPs, good clinical practices and regulatory requirements
• Proven ability to lead, manage, and motivate others in a complex, multi-functional matrix environment
• Exceptional leadership and team management skills

Must Have Skills:

• Clinical Program Management experience
• Clinical trial operations experience
• Scientific/drug development experience

Pay Transparency: The typical base pay for this role across the U.S. is: $68.00 - $70.00 /hour. Non-exempt positions are eligible for overtime at a rate of 1.5 times the base hourly rate for all hours worked in excess of 40 in a work week, or as required by state or local law. Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education and experience. Full-time employees are eligible to select from different benefits packages. Packages may include medical, denmatch, lifeion benefits, health savings accounts with qualified medical plan enrollment, 10 paid days off, 3 days paid bereavement leave, 401(k) plan participation with employer match, life and disability insurance, commuter benefits, dependent care flexible spending account, accident insurance, critical illness insurance, hospital indemnity insurance, accommodations and reimbursement for work travel, and discretionary performance or recognition bonus. Sick leave and mobile phone reimbursement provided based on state or local law.

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