Clinical Trial Manager

🔥 8 minutes ago

🌐 Serbia, Hungary, +3 more countries – Remote

🇷🇸 Serbia – Remote 🇭🇺 Hungary – Remote 🇵🇱 Poland – Remote 🇷🇴 Romania – Remote 🇸🇰 Slovakia – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 21%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Manage and operationally deliver clinical elements within trials, including site selection, start-up, enrollment 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 • Collaborate closely with cross-functional team members • Mentor and train team members • Identify challenges to study timelines and deliverables and provide creative action plans to the team and sponsor • Lead CRAs in site relationships and oversight of monitoring, regulatory, IP, site payment, and site correspondence activities • Maintain focus on study priorities through cross-functional partnerships and effective communication • 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 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 • 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 English • 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 clinical development plan execution • Mastery of ICH-GCP, relevant Precision SOPs, and regulatory guidance • Candidates must be legally authorized to work in the country of employment without employer sponsorship

🏖️ Benefits

• Remote work option • Mentoring and training of team members • Equal Opportunity Employer • Reasonable accommodation available during the application process