Senior Feasibility Associate / Feasibility Manager

4 months, 1 week ago
Full-time
Senior
Project and Program Management
Precision Medicine Group

Precision Medicine Group

Precision Medicine Group specializes in precision medicine, utilizing targeted expertise and data insights to accelerate drug development and enhance the commercialization of next-generation medical products for the pharmaceutical and life sciences ind...

Pharmaceuticals
251-1K
Founded 2012

Description

  • Provide pre-award feasibility analysis for RFPs, including competitive, recruitment, standards of care, drug, epidemiology, site, and country analyses.
  • Review clinical protocols, study assumptions, client information, and study plans for US and global trials.
  • Present feasibility findings, recommendations, and rationale to business development teams and clients.
  • Collaborate with internal colleagues, consultants, partners, and external sources to gather and share feasibility information.
  • Conduct feasibility site outreach for pre-award opportunities.
  • Support post-award, rescue, and standalone feasibility deliverables in line with study and client requirements.
  • Engage with patient advocacy groups and site networks when appropriate to support feasibility, recruitment, and study delivery.
  • Analyze site data to support site identification, enrollment modeling, and study strategy.
  • Participate in business development and client calls.
  • Support newly awarded and ongoing projects with feasibility input and site identification.

Requirements

  • Bachelor’s degree in a life sciences discipline.
  • Minimum of 5 years of related experience.
  • Relevant experience in feasibility analysis and site identification.
  • Ability to communicate professionally in English, both verbally and in writing.
  • Postgraduate degree preferred.
  • Combination of qualifications and equivalent relevant experience may be accepted.
  • Strong management and organizational skills.
  • Strong analytical thinking and rationale development skills.
  • Strong IT platform and data analysis skills.
  • Advanced computer skills with MS Word, Excel, PowerPoint, and web/data-based platforms.
  • Demonstrated knowledge of ICH-GCP.
  • Ability to work independently and as part of a matrixed, dynamic team.

Benefits

  • Fully remote role available in the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia.
  • Opportunity to work on pre-award, post-award, rescue, and standalone feasibility projects.
  • Exposure to innovative clinical trial work across oncology and rare disease.
  • Work within a scientifically driven team supporting biotech and pharma clients.
  • Equal opportunity employer policies and reasonable accommodation support for applicants.

Interested in this position?

Apply directly on the company website

Apply Now

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