Senior Project Manager – Oncology

This is a fully remote position, open to applicants in North Carolina.

📋 Description

• Oversee both core and extended cross-functional project teams throughout assigned clinical trials

• Facilitate coordination among internal partners, clients, vendors, and subcontractors

• Manage clinical trials from Phase I to IV, from initiation to closure

• Ensure accountability for project scope, timelines, quality, costs, and deliverables

• Create and maintain project plans, resource strategies, and contingency plans

• Oversee project budgets and strive to meet established financial objectives

• Assess complex project challenges and implement effective solutions

• Foster strong client relationships as a primary project liaison

• Maintain open communication to ensure client expectations are fulfilled

• Address project and team challenges through effective communication, negotiation, prioritization, and conflict resolution

• Enhance project delivery efficiency and quality

• Ensure teams adhere to clinical research standards and standard operating procedures (SOPs)

⛳️ Requirements

• A university or college degree, ideally in life sciences, or certification in a relevant allied health profession such as nursing, medical technology, or laboratory technology

• An equivalent combination of education and experience that provides the necessary knowledge and skills will also be accepted

• Minimum of 7 years of experience in the clinical pharmaceutical industry, showcasing clinical project management capabilities; alternatively, more than 5 years of supervisory experience in a healthcare environment combined with 6 years of clinical research experience in the pharmaceutical or CRO sectors

• Proven track record in managing or leading multidisciplinary project teams

• Comprehensive understanding of project management processes and experience with project management software

• Strong financial insight, including knowledge of project budgets

• Effective negotiation and commercial skills

• In-depth knowledge of ICH Guidelines and Good Clinical Practice (GCP)

• Familiarity with international regulatory requirements for clinical development programs

• Extensive knowledge of the drug development lifecycle

• Strong leadership, communication, organizational, prioritization, and relationship-building abilities

• Capability to work independently and effectively across diverse cultures

• Proficiency in English, both written and verbal, as well as fluency in the local office language

• Willingness to travel domestically and internationally, including overnight stays

• Valid and current passport

• Valid driver's license

🏝️ Benefits

• Competitive benefits package based on location

• An inclusive and equitable work environment

• Transparent compensation structures

• Equal employment opportunities