Feasibility Manager
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Feasibility Manager delivering evidence-based clinical-trial feasibility assessments for Precision for Medicine. Translating clinical, scientific, and operational data into country, site, patient-pool, and recruitment recommendations.
Responsibilities:
- Deliver evidence-based feasibility assessments across pre-award, post-award, rescue, and stand-alone engagements
- Combine clinical and scientific interpretation with operational intelligence and data analysis
- Develop country, site, patient-pool, and recruitment recommendations
- Partner with Business Development, Clinical Operations, Medical, and other cross-functional stakeholders
- Manage assigned feasibility deliverables
- Present analyses and recommendations to internal stakeholders and clients
- 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 country, site, enrolment, and operational recommendations
- Develop rationales for assumptions and identify 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
- Plan, coordinate, and analyse targeted site and investigator outreach
- Participate in bid-defence meetings and client discussions
- Contribute to feasibility methods, data sources, tools, templates, and best practices
- Share knowledge and support development of colleagues within the Feasibility team
- Work across functions, therapeutic areas, and geographic regions
- Contribute to initiatives strengthening Precision for Medicine’s scientifically driven approach and client offering
Requirements:
- 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
- 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
- Postgraduate degree in life sciences, public health, epidemiology, data science, or a related discipline (preferred)
- Experience supporting global clinical trials (preferred)
- Experience in oncology, rare disease, or other complex clinical-development programs (preferred)
- Experience presenting analyses and recommendations to clients or senior stakeholders (preferred)
- Familiarity with clinical-trial intelligence, epidemiology, site-performance, or claims and real-world-data platforms (preferred)
Benefits:
- Fully remote work arrangement
- Opportunity to contribute to complex oncology and rare-disease clinical development programs
- Work with clinical-trial execution, scientific expertise, laboratory capabilities, and advanced data sciences
- Equal Opportunity Employer
- Reasonable accommodation available during the application process
Similar Jobs
Lead Clinical Research Associate
Lead CRA overseeing regional clinical trial quality for PSI CRO, a global contract research organization. Mentoring monitors and coordinating compliance, data integrity, and study operations remotely.
Senior Clinical Research Associate – CNS/Oncology
Senior Clinical Research Associate managing CNS/Oncology clinical studies for Worldwide Clinical Trials, a global CRO. Overseeing site start-up, maintenance, compliance, and study closeout across the UK.
Senior Clinical Research Associate – CNS/Oncology
Senior Clinical Research Associate managing UK CNS/Oncology clinical research sites for global CRO Worldwide Clinical Trials. Overseeing study start-up, site maintenance, safety reporting, and closeout.
Senior Clinical Research Associate
Senior Clinical Research Associate advancing AbbVie’s oncology medicines through clinical site oversight in China. Ensuring trial compliance, data integrity, patient safety, recruitment and investigator partnerships.
Clinical Trial Manager
Clinical Trial Manager coordinating clinical research project delivery at ICON. Leading teams, managing timelines and budgets, and ensuring quality outcomes for faster patient access to medicines.
Clinical Research Associate I
Clinical Research Associate conducting onsite monitoring, site management, and regulatory support for a global medical research company. Ensuring participant safety, data quality, and study timelines across therapeutic indications.
Clinical Research Associate
Clinical Research Associate monitoring oncology and hematology clinical trials for BeOne Medicines. Managing sites, compliance, recruitment, data quality, and study milestones across Spain.
Experienced Global Study Manager – Clinical Research, Central Labs Services
Global Study Manager overseeing complex clinical trials for Labcorp’s central laboratory services. Managing client relationships, budgets, risks, milestones, and cross-functional study delivery.
Senior Clinical Research Associate
Senior Clinical Research Associate monitoring AbbVie oncology trials and supporting investigative sites in China. Driving site engagement, recruitment, compliance, risk management, and CRA mentorship.
Clinical Research Associate
Clinical Research Associate advancing AbbVie’s innovative oncology medicines pipeline. Monitoring investigative sites, ensuring compliance, data integrity, patient safety, and recruitment performance.
Clinical Research Associate II
Clinical Research Associate II advancing AbbVie’s oncology medicine pipeline through investigative-site monitoring. Supporting recruitment, compliance, data integrity and patient safety across clinical trials.
Clinical Research Associate II
Clinical Research Associate II advancing AbbVie’s oncology clinical trials in China. Monitoring investigative sites, ensuring data integrity, compliance, recruitment, and patient safety.
Clinical Research Associate II
Clinical Research Associate II advancing AbbVie’s oncology medicines through investigator partnerships and clinical site monitoring in China. Ensuring protocol compliance, patient safety, data integrity and study performance.
Clinical Research Associate II
Clinical Research Associate II advancing AbbVie’s innovative medicines through immunology trials. Managing investigative sites, monitoring compliance, data integrity, recruitment and patient safety.
Senior Clinical Research Associate
Senior Clinical Research Associate advancing AbbVie’s oncology clinical trials at AbbVie. Monitoring sites, protecting data integrity, ensuring compliance, and mentoring junior CRAs.
Senior Clinical Research Associate – FSP
Senior Clinical Research Associate monitoring clinical trials for Thermo Fisher Scientific’s global life-science solutions. Ensuring protocol compliance, data quality, site management and audit readiness.
Feasibility Manager
Feasibility Manager delivering evidence-based clinical-trial feasibility assessments for Precision for Medicine. Developing country, site, patient-pool, and recruitment recommendations for life sciences organizations.
Feasibility Manager
Feasibility Manager assessing clinical-trial feasibility for Precision for Medicine. Analyzing recruitment, site, country, epidemiology, and patient-pool data for life sciences clients.
Feasibility Manager
Feasibility Manager assessing clinical-trial recruitment, sites, and patient pools for life sciences organizations. Translating clinical and epidemiological data into evidence-based recommendations.
Feasibility Manager
Feasibility Manager assessing clinical-trial recruitment, sites, countries, and patient pools for Precision for Medicine. Presenting evidence-based recommendations supporting life sciences clinical development.