Feasibility Manager

🕒 September 1

🌐 Spain, United Kingdom, +5 more countries – Remote

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

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 35%

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

• Lead or contribute to feasibility assessments for client requests for proposals • Review clinical protocols, study assumptions, client information, and operational plans for United States and global clinical trials • Conduct and synthesise competitive landscape, historical recruitment, standard-of-care, treatment landscape, epidemiology, country, site, and patient-pool analyses • Translate evidence into clear country, site, enrolment, and operational recommendations • Develop logical, transparent rationales for assumptions and identify important data limitations and feasibility risks • Present feasibility methods, findings, recommendations, and supporting rationale to Business Development colleagues, proposal teams, and clients • Collaborate with internal colleagues, external consultants, data partners, investigators, and sites to gather and interpret feasibility information • Plan, coordinate, and analyse targeted site and investigator outreach, as appropriate • Participate in bid-defence meetings and client discussions • Contribute to the continued development of feasibility methods, data sources, tools, templates, and best practices • Share knowledge and support the development of colleagues within the Feasibility team • Work effectively across functions, therapeutic areas, and geographic regions • Contribute to initiatives that strengthen Precision for Medicine’s scientifically driven approach and client offering

🎯 Requirements

• Bachelor’s degree in life sciences or a related discipline • At least two years of relevant experience in clinical trial feasibility, clinical operations, site intelligence, epidemiology, clinical research, or a related area • Experience conducting or contributing to clinical trial feasibility analysis and site or country identification • Ability to interpret clinical, scientific, epidemiological, and operational information and develop clear recommendations • Professional proficiency in written and spoken English • Equivalent combinations of education, qualifications, and relevant experience may be considered • Postgraduate degree in life sciences, public health, epidemiology, data science, or a related discipline preferred • Experience supporting global clinical trials preferred • Experience in oncology, rare disease, or other complex clinical-development programs preferred • Experience presenting analyses and recommendations to clients or senior stakeholders preferred • Familiarity with clinical-trial intelligence, epidemiology, site-performance, or claims and real-world-data platforms preferred • Strong analytical and critical-thinking skills, with the ability to synthesize multiple evidence sources • Ability to develop and communicate a clear rationale for feasibility assumptions and recommendations • Strong attention to detail while maintaining awareness of the overall study strategy • Ability to manage multiple concurrent deliverables, stakeholders, priorities, and deadlines • Excellent written, verbal, and presentation skills • Advanced proficiency in Microsoft Excel, PowerPoint, and Word • Confidence working with web-based data, intelligence, and analytics platforms • Strong ownership of deliverable quality, accuracy, and timeliness • Collaborative working style and ability to operate effectively in a matrix environment • Ability to work independently while seeking input and escalation appropriately • Working knowledge of ICH-GCP principles

🏖️ Benefits

• Fully remote work arrangement • Opportunity to contribute to complex clinical programs in oncology and rare diseases • Opportunity to work with clinical-trial execution, scientific expertise, laboratory capabilities, and advanced data sciences • Equal Opportunity Employer