Clinical Trial Manager

🔥 4 minutes ago

🌐 Spain, Hungary, +5 more countries – Remote

🇪🇸 Spain – Remote 🇭🇺 Hungary – Remote 🇵🇱 Poland – Remote 🇷🇴 Romania – Remote 🇷🇸 Serbia – Remote 🇸🇰 Slovakia – Remote 🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

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Precision For Medicine

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $75M Private Equity Round on 2015-12

Healthcare • Consulting • Logistics

Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.

📋 Description

• Manage and operationally deliver the clinical elements of trials, including site selection, start-up, enrolment management, site engagement and support, monitoring planning and execution, data cleaning, and close-out • Execute assigned trials successfully and ensure completion of trial deliverables • Ensure appropriate communication, regulatory documentation, and ongoing oversight of assigned trials in collaboration with cross-functional team members • Mentor and train team members • Identify challenges to study timelines and deliverables and offer creative action plans to the team and sponsor • Lead CRAs in establishing site relationships and overseeing monitoring, regulatory, investigational product, site payment, and site correspondence activities • Maintain focus on study priorities through cross-functional partnerships and effective communication to achieve client satisfaction • Serve as the central intelligence hub for managed studies and oversee clinical aspects across multiple countries

🎯 Requirements

• Bachelor’s degree or equivalent combination of education/experience in science or health-related field, including experience in the field of oncology • Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, Pharma, or Biotech company in a dedicated clinical lead role • Significant clinical trial management experience in oncology • Experience with CAR-T and Radiopharmaceuticals would be a strong plus • Working knowledge of GCP/ICH guidelines and the clinical development process • Availability for domestic and international travel including overnight stays • Must be able to communicate effectively in the English language • Demonstrated computer skills with MS Office, MS Project, and PowerPoint • Software experience with CTMS, eTMF, EDC, and IXRS • Demonstrated ability to develop positive working relationships with internal and external organizations • Core understanding of medical terminology and clinical trial activities related to executing a clinical development plan • Mastery knowledge of ICH-GCP, Precision SOPs, and regulatory guidance • Must be legally authorized to work in the country of employment without employer sponsorship

🏖️ Benefits

• Remote work arrangement • Opportunities for continued professional growth • Mentoring and training of team members • Domestic and international travel opportunities

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