Allucent
Allucent
Allucent is a consulting and healthcare partner that helps small and mid-sized biotech companies advance therapies through the drug development process. Its services span clinical development, clinical pharmacology, regulatory strategy, drug safety, and pharmacovigilance, supporting programs from early research and clinical trials through post-marketing surveillance. With more than 30 years of experience and expertise across areas including oncology, infectious disease, neurology, autoimmune conditions, and rare diseases, Allucent works with biotech teams to address the scientific, regulatory, and operational challenges of bringing new treatments to market.

Strategic Feasibility Manager II — Allucent, Belgrade Hybrid

Lead clinical-trial feasibility analyses covering country and site selection, enrollment forecasting, and patient recruitment strategy. Support Allucent’s business development proposals and client feasibility discussions with evidence-based recommendations.

Description

  • Develop and oversee country and site selection recommendations, enrollment forecasts, and patient recruitment strategies
  • Validate data integrity and accurately interpret findings used in feasibility strategies and reports
  • Partner with Business Development and Allucent Centers of Expertise
  • Contribute to proposals and business development materials, including assumptions, budgets, timelines, countries, sites, and patient projections
  • Identify regions with significant disease prevalence and build initial country pools
  • Assess disease or syndrome incidence and prevalence
  • Evaluate competing clinical-trial activity to identify feasibility constraints and enrollment barriers
  • Use public and proprietary databases to assess comparable patient populations and therapeutic areas
  • Assess comparator-drug availability and reimbursement conditions in proposed countries
  • Communicate Allucent’s global and regional capabilities and study footprint
  • Present feasibility findings to Business Development teams and clients, including at bid-defense meetings
  • Maintain internal feasibility resources, libraries, and databases
  • Collaborate effectively with Centers of Expertise and Business Development teams
  • Keep current with applicable guidelines and relevant technologies
  • Report to the GSSU Site & Patient Engagement department

Requirements

  • Bachelor’s degree in life sciences or a related field
  • At least five years of experience in drug development, clinical research, or an equivalent combination of education, training, and experience
  • Proven experience analyzing large datasets
  • Experience with pre-award feasibility is advantageous
  • Willingness to travel approximately 15–20% for Business Development meetings may be required
  • Strong written and verbal communication skills, with good command of English
  • Working knowledge of government, international, open-source, and proprietary databases such as PubMed/Medline, ClinicalTrials.gov, and Citeline
  • Ability to interpret data sources and turn findings into clear, practical recommendations
  • Ability to perform effectively in a fast-paced, demanding environment within a growing company
  • Proficiency with computer applications including Word, Excel, and PowerPoint

Benefits

  • Comprehensive benefits package tailored to the employee’s location
  • Competitive compensation based on location
  • Departmental study and training budget to support professional development
  • Reasonably flexible working hours
  • Participation in the Buddy Program as a new or existing employee
  • Internal development opportunities and career progression
  • Financial rewards through the internal employee referral program
  • Eligibility for the Spot Bonus Award Program recognizing exceptional project contributions
  • Eligibility for the Loyalty Award Program recognizing long-term commitment

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