Feasibility Manager

Posted 7 Days Ago
Be an Early Applicant
Hiring Remotely in România
Remote
Junior
Healthtech • Pharmaceutical
The Role
The Feasibility Manager conducts evidence-based assessments for clinical trials, analyzing protocols, recruitment history, epidemiology, site capabilities, patient pools, and operational risks. They translate findings into country, site, enrollment, and recruitment recommendations; present analyses to clients and internal stakeholders; coordinate site and investigator outreach; support bid defenses; and improve feasibility methods, tools, data sources, and best practices. The role requires cross-functional collaboration across clinical operations, medical, business development, and external partners.
Summary Generated by Built In

Due to our continued growth, Precision for Medicine is looking for a Senior Feasibility Associate/Feasibility Manager to join our European team. This position can be covered fully remotely in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia. The final title, Senior Feasibility Associate or Feasibility Manager, will be determined based on the successful candidate’s experience and demonstrated level of responsibility.

Position Summary:

The Feasibility Manager is a member of Precision for Medicine’s expert Feasibility Department and is responsible for delivering evidence-based feasibility assessments across pre-award, post-award, rescue, and stand-alone engagements.

The role combines clinical and scientific interpretation with operational intelligence and data analysis to develop country, site, patient-pool, and recruitment recommendations. The Feasibility Manager partners with Business Development, Clinical Operations, Medical, and other cross-functional stakeholders to ensure that recommendations are scientifically credible, operationally realistic, and clearly communicated.

The successful candidate will manage assigned feasibility deliverables, present analyses and recommendations to internal stakeholders and clients, and contribute to strategic initiatives that strengthen Precision for Medicine’s feasibility capabilities and competitive position.

Key responsibilities

  • 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.

Required qualifications and experience:

  • 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.

Preferred qualifications and experience

  • Postgraduate degree in life sciences, public health, epidemiology, data science, or a related discipline.
  • Experience supporting global clinical trials.
  • Experience in oncology, rare disease, or other complex clinical-development programs.
  • Experience presenting analyses and recommendations to clients or senior stakeholders.
  • Familiarity with clinical-trial intelligence, epidemiology, site-performance, or claims and real-world-data platforms.

Skills

  • 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.

Precision for Medicine brings together clinical-trial execution, scientific expertise, laboratory capabilities, and advanced data sciences to help life sciences organizations improve the speed, cost, and likelihood of successful clinical development. The organization has a strong focus on oncology and rare diseases and offers the opportunity to contribute to complex programs that seek to bring meaningful therapies to patients.


Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.

Skills Required

  • 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
  • Postgraduate degree in life sciences, public health, epidemiology, data science, or a related discipline
  • Experience supporting global clinical trials
  • Experience in oncology, rare disease, or other complex clinical-development programs
  • Experience presenting analyses and recommendations to clients or senior stakeholders
  • Familiarity with clinical-trial intelligence, epidemiology, site-performance, or claims and real-world-data platforms
  • Advanced proficiency in Microsoft Excel, PowerPoint, and Word
  • Working knowledge of ICH-GCP principles

Precision Medicine Group Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Precision Medicine Group and has not been reviewed or approved by Precision Medicine Group.

  • Healthcare Strength Health coverage includes medical, dental, and vision with HSA/FSA options, plus disability and life insurance, forming a comprehensive core package. The lineup is presented as robust across wellbeing, time off, and financial security categories.
  • Leave & Time Off Breadth Time off includes generous PTO and paid holidays, along with paid parental leave and adoption assistance. These offerings are positioned as part of a well-rounded benefits suite in the U.S. with similar cores noted in Canada.
  • Retirement Support Retirement programs include a 401(k) with employer match in the U.S. and a group retirement plan in Canada. These elements help establish a competitive total rewards foundation.

Precision Medicine Group Insights

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The Company
HQ: Bethesda, MD
396 Employees
Year Founded: 2012

What We Do

We founded Precision Medicine Group in 2012 because we believed there was a transformational opportunity to improve the process of bringing new drugs to market. It involves utilizing technology, data, and human expertise. It is a big challenge that requires diverse talents. Our model involves both nurturing and investing organically and acquiring capabilities that we do not have but critically need. Our core executive team is anchored to this model, building life science services that address fundamental changes in healthcare that are necessary for health and outcomes improvement.

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