Senior Project Manager – Oncology

🕒 vor 26 Tagen

🇺🇸 Vereinigte Staaten – Remote

💵 $147.300 - $220.900 / Jahr

⏰ Vollzeit

🟠 Senior

👷‍♀️ Projektmanager

🦅 H1B-Visum-Sponsor

Dieses Unternehmen hat in der Vergangenheit H1B-Visa gesponsert.

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Precision Medicine Group

WebsiteLinkedInAlle Stellen

1001 - 5000 Mitarbeiter

Gegründet 2012

🧬 Biotechnologie

⚕️ Krankenversicherung

💊 Pharmazie

💰 €35.200.000 Venture Round im 2021-03

Biotechnology • Healthcare Insurance • Pharmaceuticals

Precision Medicine Group ist ein globales Expertenteam, das sich auf Präzisionsmedizin spezialisiert – eine Disziplin, die fortgeschrittene Laborwissenschaften, translationale Informatik, Regulatory Affairs, Payer Insights und Marketingkommunikation verbindet. Das Unternehmen konzentriert sich darauf, Herausforderungen in der Produktentwicklung und Kommerzialisierung für Kunden aus der Pharma- und Life-Sciences-Branche zu bewältigen. Die Services umfassen biomarkergetriebene Forschung und Entwicklung sowie Unterstützung bei der Kommerzialisierung für Life-Science-Organisationen – vom Launch bis zur Produktreife. Die Precision Medicine Group agiert über zwei Hauptgeschäftsbereiche: Precision for Medicine und Precision AQ, die jeweils auf klinische bzw. kommerzielle Lösungen spezialisiert sind.

Beschreibung

• The Senior Project Manager plans, directs, coordinates, and delivers activities for designated clinical study projects to ensure that project objectives of quality, scope, cost, and time are accomplished. • Serve as primary point-of-contact and primary escalation point to the client • Coordinate and oversees all functional services including external vendors to the established timeline and budget • Manage the study budget, ensuring project remains within scope and that any out of scope activities are identified early and handled as appropriate. • Maintain integrated collaboration with clinical operations in the delivery and participates in clinical activities as appropriate. • Develop robust and comprehensive project plans, including timelines and proactive risk management and mitigation, to guide all parameters of trial execution with consistency and quality • Ensure Quality management for assigned projects, including eTMF Inspection readiness, implementation of quality notification incident forms and / or corrective and preventative action plans to address any quality findings. • Maintain integrated collaboration with all functional operations in the delivery of the program and review as necessary of other study documentation • Establish tracking metrics to monitor trial and team progress towards project goals • Prepare project status updates and report on progress to clients and senior management, including reporting on key performance indicators, offering solutions and opportunities as they arise • Leads both internal and client meetings and set expectations for the project team • Communicate effectively with client and Precision management to relay protocol/study issues including any deviations and implements necessary actions in response to those issues • Ability to conduct formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients including Bid Defenses with proficiency • Ensure study specific training is implemented in collaboration with functional areas and ensure study specific training compliance for the duration of the project • Support business development and marketing activities as appropriate, including travel to Bid Defense meetings as required • Perform other duties as assigned by management • Remain compliant with organizational training, time-reporting and any other administrative duties as required • Provides on-going feedback, for functional team members including annual performance reviews

🎯 Anforderungen

• North America: Bachelor’s degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred • EU: Degree or equivalent combination of education/experience in science or health-related field. Advanced degree preferred • Minimum of 7 years of clinical research experience or proven competencies for this position and a minimum of 4 years of direct project management experience • Experience in managing complex and global trials • Ability to travel domestically and internationally including overnight stays • Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint) Microsoft Project, eTMF, EDC and CTMS • Proven communication and interpersonal skills to effectively interface with others in a team setting • Proven organizational skills, attention to detail, and a customer service demeanor

🏖️ Vorteile

• Health insurance • Retirement savings benefits • Life insurance • Disability benefits • Parental leave • Paid time off for sick leave and vacation