
Project Manager, Internal Medicine
Posted Aug 26

Posted Aug 26
This is a fully remote position, open to applicants in United States, +2 more locations.
• Oversee one or multiple assigned Phase I through IV clinical trials with local, regional, or global focus.
• Organize and manage clinical trials from initiation to closure.
• Direct the technical, financial, and operational facets of projects.
• Identify and assess project needs, interpret complex data, and formulate contingency plans and rescue strategies.
• Ensure that project outcomes align with customer expectations regarding time, quality, cost, and contract specifications.
• Lead core project team members and foster leadership within extended or complete project teams.
• Guide internal and external cross-unit coordination, including subcontractors.
• Define and oversee project resource requirements in conjunction with functional heads and establish contingency strategies.
• Design, execute, monitor, and modify project plans as necessary.
• Encourage effective teamwork and address conflicts.
• Maintain appropriate communication with Project Management leadership.
• Bachelor’s degree (preferably in life sciences) or certification in a related allied health profession from an accredited institution, or an equivalent 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 setting along with four (4) years of clinical research experience in the pharmaceutical or CRO sectors, or demonstrated relevant clinical development experience and competencies.
• Experience in managing projects within a multi-office environment.
• Capability to manage multiple competing priorities and effectively utilize resources.
• Ability to inspire teamwork and motivate personnel within a matrix organization.
• Capacity to lead by example and encourage team members to seek solutions.
• Exceptional communication, planning, and organizational abilities.
• Self-driven with strong problem-solving skills.
• Comprehensive understanding of project management processes.
• In-depth knowledge of ICH Guidelines and GCP, including international regulatory standards.
• Willingness to travel domestically and internationally, including overnight stays.
• A valid current passport is required.
• Must possess a valid driver's license and the ability to drive.
• Proficient in the local office language and English, both written and verbal.
• Broad understanding of drug development processes and client requirements.
• Competitive benefits package based on location.
• An inclusive and equitable workplace.
• Transparent compensation and pay equity.
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