EMD Serono
Sr. Director, Compound Operational Lead(m/w/x)
Full-timeWith HomeofficeSenior
Eysins
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SUSUSONITY
Associate Director, Trial Clinical Delivery Lead(m/w/x)
Eysins
Full-timeWith Home OfficeManagement
Nejo AI Summary
Global clinical trial delivery for new medicines and smart devices in oncology, neurology, or fertility. 8-10 years clinical operations project management experience required. High autonomy in trial delivery.
Requirements
- Bachelor’s Degree in Medical or Life Sciences
- 8-10 years clinical operations project management
- Expert knowledge of clinical development regulations
- Oncology, Neurology, or Immunology TA experience
- Clinical operations experience in CRO or pharma
- Strong interpersonal and communication skills
- Strategic thinking and influencing skills
- Ability to work independently
- Aptitude for interpreting analytical tools
- Risk assessment and decision-making ability
- Ability to oversee multiple tasks simultaneously
- Comfortable in fast-paced environments
Tasks
- Lead global clinical trial delivery and site performance
- Oversee site and vendor performance metrics
- Mitigate study risks and resolve operational issues
- Drive innovative methodologies and value-adding solutions
- Execute site and patient engagement strategies
- Coordinate between site leads and global functions
- Provide strategic oversight for Phase I-IIIb studies
- Promote data-driven planning and accountability
- Implement operational excellence strategies across studies
- Escalate trends and risks to senior management
- Onboard and train new clinical team members
- Facilitate regular communication with site stakeholders
- Lead process improvement and best practice initiatives
- Represent site management in clinical trial teams
- Assess data-driven proposals for country and site selection
- Integrate patient and physician insights into study design
- Design country start-up and recruitment strategies
- Implement decentralized clinical trial and digital solutions
- Manage service providers' timelines, budget, and quality
- Develop risk-based monitoring and site oversight plans
- Analyze performance data to ensure study quality
- Participate in investigator and study coordinator meetings
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Career Advancement
- Access and development opportunities
Informal Culture
- Culture of inclusion and belonging
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SUSONITY and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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SUSUSONITY
Associate Director, Trial Clinical Delivery Lead(m/w/x)
Eysins
Full-timeWith Home OfficeManagement
Nejo AI Summary
Global clinical trial delivery for new medicines and smart devices in oncology, neurology, or fertility. 8-10 years clinical operations project management experience required. High autonomy in trial delivery.
Requirements
- Bachelor’s Degree in Medical or Life Sciences
- 8-10 years clinical operations project management
- Expert knowledge of clinical development regulations
- Oncology, Neurology, or Immunology TA experience
- Clinical operations experience in CRO or pharma
- Strong interpersonal and communication skills
- Strategic thinking and influencing skills
- Ability to work independently
- Aptitude for interpreting analytical tools
- Risk assessment and decision-making ability
- Ability to oversee multiple tasks simultaneously
- Comfortable in fast-paced environments
Tasks
- Lead global clinical trial delivery and site performance
- Oversee site and vendor performance metrics
- Mitigate study risks and resolve operational issues
- Drive innovative methodologies and value-adding solutions
- Execute site and patient engagement strategies
- Coordinate between site leads and global functions
- Provide strategic oversight for Phase I-IIIb studies
- Promote data-driven planning and accountability
- Implement operational excellence strategies across studies
- Escalate trends and risks to senior management
- Onboard and train new clinical team members
- Facilitate regular communication with site stakeholders
- Lead process improvement and best practice initiatives
- Represent site management in clinical trial teams
- Assess data-driven proposals for country and site selection
- Integrate patient and physician insights into study design
- Design country start-up and recruitment strategies
- Implement decentralized clinical trial and digital solutions
- Manage service providers' timelines, budget, and quality
- Develop risk-based monitoring and site oversight plans
- Analyze performance data to ensure study quality
- Participate in investigator and study coordinator meetings
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Career Advancement
- Access and development opportunities
Informal Culture
- Culture of inclusion and belonging
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SUSONITY and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
SUSONITY
Industry
Healthcare
Description
Das Unternehmen entwickelt Medikamente, intelligente Geräte und innovative Technologien in Therapiegebieten wie der Onkologie, Neurologie und Fruchtbarkeit.
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