Project Manager

Job Title

Location: 126 E Lincoln Ave, Rahway NJ Rate: $45-$50/HR on W2 Start date: 2/19/24

Qualifications

Education: Required: Bachelor's or Master's degree required in life sciences, business, or related healthcare area. No PhD. Preferred: PMP or CAPM certification

Experience and Skills: REQUIRED • Minimum of three (3) years of experience in project management, in pharmaceutical, clinical research, outcomes research or medical implementation related field • Strong interpersonal, verbal, and written communication skills to work with medical and/or scientific teams • Ability to independently handle multiple projects and priorities simultaneously and function in a fast-paced environment • Experience working effectively both independently and as part of a team • Ability to quickly and comprehensively learn about new subject areas and environments • Self-motivation, flexibility, resourcefulness, and problem-solving capabilities • Passion for science • Outstanding Microsoft Word, PowerPoint, Excel, and Teams skills PREFERRED: • Experience working globally across regions and countries • Prior experience leading large complex multi-stakeholder projects • Prior vendor management and budget-planning experience. ADDITONAL: • 3 days required onsite, Friday remote. • Local candidates only.

Responsibilities

The goal of the Value Medical Cross Team Project Manager is to provide the Value Medical Project Management (VMPM) organization with project management and in-depth knowledge of one or more areas in the execution of the integrated Value and Implementation (V&I) Plans. The Cross Team PM will be a subject matter expert and key contact for one or more specific elements of the V&I plan and provide flex capacity to the Value Team (VT) and Medical Team (MT) at various stages of product or program lifecycle, depending on the specific needs of the VTs and MTs. This role works closely with the Lead PMs in Value Medical Project Management and the global cross-functional leads in Center for Observational and Real World Evidence (CORE), Biostatistics and Research Decision Sciences (BARDs) and Global Medical Scientific Affairs (GMSA) (e.g., EDMA/GDMA) to ensure the seamless coordination and execution of all relevant aspects of the V&I Plans throughout their product and program lifecycles. The Cross Team PM will work with more than one Lead PM across product/programs.

Primary responsibilities may include one or more of the following key areas: Planning and prioritization: • Contribute to aggregation and reporting of internal and external strategic insights (e.g. X-FLY, IRMS, Medical Intelligence Dashboard) to inform the development and execution of V&I plans Therapeutic Area Product/Program Coordination: • Support the Lead PM with the gathering and synthesis of one or more components of the V&I plan (e.g., HTA dossiers, Medical Education, input meetings, etc.) • Support the planning and coordination of V&I team meetings, related communications, and community/team site stewardship • Support Lead PMs across Therapeutic Areas (TAs) for key congresses in collaboration with BARDS/CORE/GMSA stakeholders and other internal and external stakeholders • Ad hoc and special project initiatives requiring collaboration and coordination with other project managers across product/programs,, and cross-functional teams (IT, Operations) • Align external stakeholder engagement activities (e.g. EIFs, SIEs, Scientific Leader Utilization Plan (SUP)) across programs and TAs with key milestones in the V&I plan and collaborate with GEMS (where applicable) Reporting and Tracking: • Support PM Team Leader with developing, maintaining, and monitoring project plans, project schedules, budgets, and expenditures • Track above V&I project progress and provide project updates/summaries • Ensure projects adhere to frameworks and all documentation is maintained appropriately for each project • Team project initiation, budget tracking and vendor activity management Risk Management: • Proactively assess project risks and issues and provide solutions where applicable • Navigate internal processes and procedures, including compliance and finance, to ensure compliant execution of assigned projects • Ensure that all activities are in performed consistent with our company's values, standards, policies and procedures.

Interested; kindly share your updated resume with answers: 1-How many years of exp Project management exp in pharmaceutical, clinical research, outcomes research or medical implementation related field 2-How far you live from 126 E. Lincoln Avenue Rahway and are you open to do Hybrid role