Dein persönlicher KI-Karriere-Agent
Clinical Project Manager -Non Interventional Studies - Sponsor Dedicated(m/w/x)
Managing non-interventional dermatology studies for a global CRO. Experience managing observational trials required. Participation in bid defense presentations.
Anforderungen
- Bachelor's Degree in Life sciences or related field
- 5 years relevant experience including > 3 years project management experience or equivalent
- Advanced knowledge of job area and broad knowledge of related job areas
- Experience managing observational/phase IV/non interventional studies
- Experience managing Dermatology chronic inflammatory diseases trials
- Knowledge of clinical trial conduct and regulatory requirements (ICH GCP, local laws)
- Broad protocol knowledge; therapeutic knowledge desired
- Understanding of competitive environment and IQVIA solutions value
- Strong written and verbal communication skills
- Good command of English language
- Strong presentation skills
- Strong problem solving skills
- Ability to work through others to deliver results
- Monitoring/managing performance and providing feedback
- Partnering cross functionally and with customers
- Ability to make decisions and bring clarity to information
- Planning, time management and prioritization skills
- Ability to organize resources, set objectives and provide direction
- Planning activities in advance with changing circumstances
- Ability to handle conflicting priorities
- Attention to detail and accuracy
- Results-oriented approach to work
- Demonstrated learning agility and openness to learning
- Good software and computer skills
- MS Office applications (Word, Excel, PowerPoint)
- Ability to establish and maintain effective working relationships
- Strong customer service skills
- Ability to work across geographies
- High awareness and understanding of cultural differences
- Good understanding of project financials
- Experience managing contractual obligations and implications
- Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, Innovation, Ownership)
Aufgaben
- Participate in bid defense presentations
- Lead presentations for smaller, less complex studies
- Manage delivery of smaller, less complex studies
- Develop integrated study management plans
- Execute clinical studies per contract
- Optimize speed, quality, and cost of delivery
- Ensure consistent use of study tools and training materials
- Comply with standard processes, policies, and procedures
- Set objectives for core project team and sub-teams
- Communicate and assess team performance
- Collaborate with functional groups to achieve milestones
- Manage study issues and obstacles
- Monitor progress against contract
- Prepare and present project information to stakeholders
- Manage project risks and contingencies
- Lead problem-solving and resolution efforts
- Identify and respond to quality risks and issues
- Plan and implement corrective and preventative actions
- Serve as primary or backup project contact with customers
- Communicate with IQVIA business development representatives
- Build and lead cross-functional project teams
- Manage cross-collaboration of core team
- Support milestone achievement and manage study issues
- Ensure financial success of the project
- Forecast and identify revenue acceleration opportunities
- Identify and manage changes in scope
- Identify lessons learned and implement best practices
- Manage project vendor relationships and activities
- Adopt and advocate for corporate initiatives
- Provide performance feedback to line managers
- Support and mentor less experienced team members
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – fortgeschritten
Tools & Technologien
- MS Office
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
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Clinical Project Manager -Non Interventional Studies - Sponsor Dedicated(m/w/x)
Managing non-interventional dermatology studies for a global CRO. Experience managing observational trials required. Participation in bid defense presentations.
Anforderungen
- Bachelor's Degree in Life sciences or related field
- 5 years relevant experience including > 3 years project management experience or equivalent
- Advanced knowledge of job area and broad knowledge of related job areas
- Experience managing observational/phase IV/non interventional studies
- Experience managing Dermatology chronic inflammatory diseases trials
- Knowledge of clinical trial conduct and regulatory requirements (ICH GCP, local laws)
- Broad protocol knowledge; therapeutic knowledge desired
- Understanding of competitive environment and IQVIA solutions value
- Strong written and verbal communication skills
- Good command of English language
- Strong presentation skills
- Strong problem solving skills
- Ability to work through others to deliver results
- Monitoring/managing performance and providing feedback
- Partnering cross functionally and with customers
- Ability to make decisions and bring clarity to information
- Planning, time management and prioritization skills
- Ability to organize resources, set objectives and provide direction
- Planning activities in advance with changing circumstances
- Ability to handle conflicting priorities
- Attention to detail and accuracy
- Results-oriented approach to work
- Demonstrated learning agility and openness to learning
- Good software and computer skills
- MS Office applications (Word, Excel, PowerPoint)
- Ability to establish and maintain effective working relationships
- Strong customer service skills
- Ability to work across geographies
- High awareness and understanding of cultural differences
- Good understanding of project financials
- Experience managing contractual obligations and implications
- Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, Innovation, Ownership)
Aufgaben
- Participate in bid defense presentations
- Lead presentations for smaller, less complex studies
- Manage delivery of smaller, less complex studies
- Develop integrated study management plans
- Execute clinical studies per contract
- Optimize speed, quality, and cost of delivery
- Ensure consistent use of study tools and training materials
- Comply with standard processes, policies, and procedures
- Set objectives for core project team and sub-teams
- Communicate and assess team performance
- Collaborate with functional groups to achieve milestones
- Manage study issues and obstacles
- Monitor progress against contract
- Prepare and present project information to stakeholders
- Manage project risks and contingencies
- Lead problem-solving and resolution efforts
- Identify and respond to quality risks and issues
- Plan and implement corrective and preventative actions
- Serve as primary or backup project contact with customers
- Communicate with IQVIA business development representatives
- Build and lead cross-functional project teams
- Manage cross-collaboration of core team
- Support milestone achievement and manage study issues
- Ensure financial success of the project
- Forecast and identify revenue acceleration opportunities
- Identify and manage changes in scope
- Identify lessons learned and implement best practices
- Manage project vendor relationships and activities
- Adopt and advocate for corporate initiatives
- Provide performance feedback to line managers
- Support and mentor less experienced team members
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – fortgeschritten
Tools & Technologien
- MS Office
- Microsoft Word
- Microsoft Excel
- Microsoft PowerPoint
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
IQVIA
Branche
Healthcare
Beschreibung
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
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