Senior Feasibility Associate / Feasibility Manager

3 months, 2 weeks ago
Full-time
Senior
Project and Program Management
Precision For Medicine

Precision For Medicine

Precision for Medicine is a specialized scientific services company that helps pharmaceutical and life sciences clients innovate, develop, and commercialize next-generation medical products. With a diverse team of experts, they offer comprehensive serv...

Pharmaceuticals
1K-5K
Founded 2012
$225M raised

Description

  • Provide pre-award feasibility analysis for RFPs, including competitive, recruitment, standards of care, drug, epidemiology, site, and country analysis.
  • Review clinical protocols, study assumptions, client information, and study plans for US and global trials.
  • Present feasibility analyses to business development teams and clients, including recommendations and rationale.
  • Collaborate with internal and external stakeholders, consultants, and partners 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 where appropriate to support feasibility, recruitment, and delivery.
  • Analyze collected site data to support site identification, enrollment modeling, and study strategy.
  • Participate in business development and client calls.
  • Contribute to projects that support innovation and competitive positioning.

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 formal education requirements.
  • Relevant experience in feasibility analysis and site identification.
  • Professional-level English communication skills, both verbal and written.
  • Postgraduate degree preferred.
  • Strong management and organizational skills.
  • Excellent oral and written communication skills in English.
  • Strong analytical thinking and rationale development skills.
  • Strong IT platform and data analysis skills, including advanced use of MS Word, Excel, PowerPoint, and web/data-based platforms.
  • Strong presentation abilities.
  • Demonstrated knowledge of ICH-GCP.
  • Ability to work independently and in a matrix environment as part of a team.
  • Strong attention to detail with the ability to see the big picture.

Benefits

  • Fully remote work location across the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia.
  • Opportunity to work on clinical trial feasibility across biotech and pharma programs.
  • Exposure to innovative, scientifically driven work in oncology and rare disease.
  • Employment with Precision for Medicine, part of Precision Medicine Group.
  • Equal Opportunity Employer status.
  • Reasonable accommodation support during the application process.

Interested in this position?

Apply directly on the company website

Apply Now

Similar Roles

Enterprise Risk Analyst

Monzo 1K-5K Banks

Monzo is hiring an Enterprise Risk Analyst in London or remotely in the UK to support strategic risk oversight, macroeconomic analysis, and enterprise risk frameworks for its Group Risk team.

1 day, 5 hours ago

Responsible Gaming Analyst

Super Technologies Pvt Ltd 1-10 aviation & aerospace

Super Technologies is hiring a Responsible Gaming Analyst to help protect players and the business by monitoring gambling-related risk and supporting compliance across its international iGaming operations.

2 days, 5 hours ago

Finance & Operation Analyst

Really Great Reading 11-50 Diversified Consumer Services

Really Great Reading is hiring a Finance and Operations Analyst to support financial planning, reporting, forecasting, and operational analysis for a mission-driven education company.

NetSuite Power BI Tableau
3 days, 6 hours ago

Central Monitor II

Precision Medicine Group 251-1K Pharmaceuticals

Precision Medicine Group is seeking a Central Monitor II to oversee centralized monitoring and risk management for clinical trials, ensuring data quality and issue escalation across studies and portfolios.

4 days, 5 hours ago

You're on a roll! Sign up now to keep applying.

Sign Up

Already have an account? Log in

Used by 14,729+ remote workers