Senior Feasibility Associate / Feasibility Manager

4 months, 1 week ago
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 assessments.
  • 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 business development and client calls related to feasibility.
  • Deliver post-award, rescue, and standalone feasibility work in line with study and client requirements.
  • Engage with patient advocacy groups and site networks when needed to support feasibility and recruitment.
  • Analyze site data to support site identification, enrollment modeling, and study strategy.

Requirements

  • Bachelor’s degree in a life sciences discipline.
  • Minimum of 5 years of related experience.
  • Equivalent relevant qualifications and experience may be accepted in place of the stated degree and experience.
  • Relevant hands-on experience in feasibility analysis and site identification.
  • Professional-level English communication skills, both written and verbal.
  • Postgraduate degree preferred.
  • Strong management and organizational skills.
  • Strong analytical thinking and rationale development skills.
  • Strong IT, data analysis, and presentation skills.
  • Advanced computer skills in MS Word, Excel, PowerPoint, and web/data-based platforms.
  • Knowledge of ICH-GCP.
  • Ability to work independently and in a matrix environment as part of a dynamic team.

Benefits

  • Fully remote work option in the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia.
  • Opportunity to work on projects for biotech and pharma clients.
  • Exposure to innovative clinical trial execution, scientific expertise, laboratory expertise, and advanced data science.
  • Focus on oncology and rare disease programs.
  • Equal Opportunity Employer status.

Interested in this position?

Apply directly on the company website

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