Salary Range:
CHF122,500.00 – CHF227,500.00
Job Description Summary Location: Basel, Switzerland Internal Title: Strategic Feasibility Expert (SFE) Novartis is unable to offer relocation support for this role; please apply only if you can work in Basel.
The Strategic Feasibility Expert is accountable for the clinical feasibility strategy for Biomedical Research therapeutic areas (TAs) and patient trials managed by Translational Medicine. The role is a TA-aligned single point of contact to ensure study timelines and enrolment plans reflect indication footprint and site landscaping enabling successful trial execution. The Expert will lead early medical and operational feasibility, proactively identify high-quality academic and commercial sites, and engage key strategic investigators, sites and networks.
Key Responsibilities
Lead strategic identification, selection of countries and sites for given therapeutic area and clinical trials.
Provide early strategic feasibility input (medical and operational) using relevant tools, databases, and metrics.
Accountable within the Clinical Trial Team (CTT) for appropriate site identification and for anticipating and relaying hurdles and delays for consideration in selection and timelines.
Consolidate feasibility feedback and potential site list for CTT decision making; act as point of escalation when a site selection or sourcing challenge impacting trial timelines is identified.
Engage internally and externally to identify new investigators/sites; maintain knowledge of investigator/site mapping in alignment with TA/indication strategy.
Maintain awareness of site performance data such as recruitment.
Identify and maintain relationships with key strategic investigators, sites, and networks; establish strategic partnerships as appropriate.
Work closely with CTT during protocol development to understand site specifications and provide robust input into the operational plan.
Collaborate with Clinical Finance Manager on early strategic planning, site budget, timelines, and TTG impact.
Collaborate with global stakeholders, including TA Heads, Clinical Scientists, TMEs, Country Organizations, Global Clinical Operations.
Essential Requirements
At least 8 to 10 years’ experience in pharmaceutical/bio‑tech/CRO drug development environments.
Excellent understanding of the drug development process; early clinical development preferred.
Superior knowledge of clinical trials site selection, global/country specific requirements, timelines, and challenges.
Demonstrated ability to work effectively in a global, matrix organization and build strong positive relationships.
Ability to work independently, demonstrate willingness to make decisions and take responsibility.
Desirable Requirements
Advanced computer literacy.
Excellent organizational skills; ability to adjust to multiple demands, shifting priorities and unexpected events while maintaining a positive work attitude.
Benefits & Rewards Expected Annual Base Salary Range: 122,500.00 – 227,500.00 CHF. In addition to base salary, you may be eligible for a performance-based bonus and, depending on role, long‑term equity awards at the group level. Flexible and hybrid working options are available when possible. Minimum 14 weeks paid parental leave. Other benefits include insurance plans, retirement plans, wellbeing resources, and global recognition programs.
Commitment to Diversity and Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams that represent the patients and communities we serve. Pay equity is a fundamental principle of our employment policy and reflects our commitment to a diverse, equitable and inclusive environment that treats all employees with dignity and respect.
Accessibility and Accommodation Novartis is committed to providing reasonable accommodation to all individuals. If you need accommodation for any part of the recruitment process or to receive more detailed information about the essential functions of the role, please contact diversity.inclusion_ch@novartis.com and include the job requisition number.
Skills Desired
Budget Management
Clinical Research
Clinical Trial Protocols
Clinical Trials
Coaching
Cross-Functional Teamwork
Data Analysis
Learning Design
Lifesciences (Inactive)
Risk Management
Risk Monitoring
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CHF122,500.00 – CHF227,500.00
Job Description Summary Location: Basel, Switzerland Internal Title: Strategic Feasibility Expert (SFE) Novartis is unable to offer relocation support for this role; please apply only if you can work in Basel.
The Strategic Feasibility Expert is accountable for the clinical feasibility strategy for Biomedical Research therapeutic areas (TAs) and patient trials managed by Translational Medicine. The role is a TA-aligned single point of contact to ensure study timelines and enrolment plans reflect indication footprint and site landscaping enabling successful trial execution. The Expert will lead early medical and operational feasibility, proactively identify high-quality academic and commercial sites, and engage key strategic investigators, sites and networks.
Key Responsibilities
Lead strategic identification, selection of countries and sites for given therapeutic area and clinical trials.
Provide early strategic feasibility input (medical and operational) using relevant tools, databases, and metrics.
Accountable within the Clinical Trial Team (CTT) for appropriate site identification and for anticipating and relaying hurdles and delays for consideration in selection and timelines.
Consolidate feasibility feedback and potential site list for CTT decision making; act as point of escalation when a site selection or sourcing challenge impacting trial timelines is identified.
Engage internally and externally to identify new investigators/sites; maintain knowledge of investigator/site mapping in alignment with TA/indication strategy.
Maintain awareness of site performance data such as recruitment.
Identify and maintain relationships with key strategic investigators, sites, and networks; establish strategic partnerships as appropriate.
Work closely with CTT during protocol development to understand site specifications and provide robust input into the operational plan.
Collaborate with Clinical Finance Manager on early strategic planning, site budget, timelines, and TTG impact.
Collaborate with global stakeholders, including TA Heads, Clinical Scientists, TMEs, Country Organizations, Global Clinical Operations.
Essential Requirements
At least 8 to 10 years’ experience in pharmaceutical/bio‑tech/CRO drug development environments.
Excellent understanding of the drug development process; early clinical development preferred.
Superior knowledge of clinical trials site selection, global/country specific requirements, timelines, and challenges.
Demonstrated ability to work effectively in a global, matrix organization and build strong positive relationships.
Ability to work independently, demonstrate willingness to make decisions and take responsibility.
Desirable Requirements
Advanced computer literacy.
Excellent organizational skills; ability to adjust to multiple demands, shifting priorities and unexpected events while maintaining a positive work attitude.
Benefits & Rewards Expected Annual Base Salary Range: 122,500.00 – 227,500.00 CHF. In addition to base salary, you may be eligible for a performance-based bonus and, depending on role, long‑term equity awards at the group level. Flexible and hybrid working options are available when possible. Minimum 14 weeks paid parental leave. Other benefits include insurance plans, retirement plans, wellbeing resources, and global recognition programs.
Commitment to Diversity and Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams that represent the patients and communities we serve. Pay equity is a fundamental principle of our employment policy and reflects our commitment to a diverse, equitable and inclusive environment that treats all employees with dignity and respect.
Accessibility and Accommodation Novartis is committed to providing reasonable accommodation to all individuals. If you need accommodation for any part of the recruitment process or to receive more detailed information about the essential functions of the role, please contact diversity.inclusion_ch@novartis.com and include the job requisition number.
Skills Desired
Budget Management
Clinical Research
Clinical Trial Protocols
Clinical Trials
Coaching
Cross-Functional Teamwork
Data Analysis
Learning Design
Lifesciences (Inactive)
Risk Management
Risk Monitoring
#J-18808-Ljbffr
Kontaktdaten:
Healthcare Businesswomen’s Association Recruiting-Team
