Project Manager, Internal Medicine – Metabolic Live Diseases

Posted Aug 19

This is a fully remote position, open to applicants in United States, +2 more locations.

📋 Description

• Oversee one or multiple assigned Phase I through IV clinical trials, which may be conducted locally, regionally, or globally.

• Organize and manage clinical trials from initiation through to closure.

• Direct the technical, financial, and operational components of projects.

• Collaborate with functional area leaders to identify and assess project requirements.

• Analyze data related to complex issues.

• Prepare for contingencies and implement rescue strategies when necessary.

• Ensure that solutions are executed, and project deliverables align with customer expectations for time, quality, and cost.

• Guide core project team members and facilitate the leadership of extended or complete project teams.

• Lead internal and external cross-unit coordination, including subcontractors.

• Define and manage project resource needs alongside functional heads.

• Develop contingency plans for essential resources.

• Ensure effective design, implementation, tracking, and revision of project plans.

• Foster effective teamwork and address conflicts.

• Communicate project-related updates to Project Management leadership.


⛳️ Requirements

• University or college degree (preferably in life sciences) or certification in a related allied health profession from a recognized institution, or a suitable combination of education and experience.

• At least five (5) years of experience in the clinical pharmaceutical industry, including clinical project management responsibilities.

• Alternatively, more than five (5) years of supervisory experience in a healthcare environment and four (4) years of clinical research experience in the pharmaceutical or CRO sectors, or demonstrated relevant clinical development experience and skills.

• In-depth knowledge of project management processes.

• Strong understanding of ICH Guidelines and GCP, including international regulatory standards.

• Willingness to travel domestically and internationally, including overnight stays.

• A valid current passport is required.

• Capability to drive and possess a valid driver’s license.

• Proficiency in the local office language and English, both written and verbal.

• Comprehensive understanding of drug development processes and client needs.

• Experience managing projects in a multi-office environment.

• Ability to manage multiple competing priorities and utilize resources effectively.

• Skill in inspiring teamwork and motivating staff within a matrix system.

• Capacity to lead by example and encourage team members to find solutions.

• Exceptional communication, planning, and organizational abilities.


🏝️ Benefits

• Competitive benefits package based on location.

• Transparent compensation and pay equity.

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