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Senior Clinical Project Scientist(m/w/x)
Scientific partnership with Clinical Project Physician, authoring core trial documents, and engaging external experts. Advanced degree in life/health sciences and extensive pharma/CRO experience required. 4-day work week, company car for private use.
Requirements
- Advanced degree in life or health sciences
- Extensive experience in pharmaceutical company or CRO
- Strong exposure to Phase II–III clinical trials
- Proven experience authoring and reviewing scientific documents
- Proven experience authoring and reviewing clinical trial documents
- Solid understanding of clinical trial design
- Solid understanding of statistics
- Solid understanding of regulatory requirements
- Solid understanding of drug development processes
- Confidence in working within global teams
- Confidence in working within cross-functional teams
- Fluent English (written and spoken)
- Structured working style
- Proactive working style
- Results-oriented working style
Tasks
- Partner scientifically with the Clinical Project Physician
- Lead or contribute to authoring core trial documents
- Provide scientific input for medical monitoring and data review
- Engage with external clinical experts and organize meetings
- Contribute to regulatory interactions
- Support lifecycle management from early to post-approval stages
- Mentor and provide clinical leadership
- Participate in business development and due diligence activities
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Fluent
Benefits
Competitive Pay
- Competitive salaries
Informal Culture
- Inclusive environment
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Senior Clinical Project Scientist(m/w/x)
Scientific partnership with Clinical Project Physician, authoring core trial documents, and engaging external experts. Advanced degree in life/health sciences and extensive pharma/CRO experience required. 4-day work week, company car for private use.
Requirements
- Advanced degree in life or health sciences
- Extensive experience in pharmaceutical company or CRO
- Strong exposure to Phase II–III clinical trials
- Proven experience authoring and reviewing scientific documents
- Proven experience authoring and reviewing clinical trial documents
- Solid understanding of clinical trial design
- Solid understanding of statistics
- Solid understanding of regulatory requirements
- Solid understanding of drug development processes
- Confidence in working within global teams
- Confidence in working within cross-functional teams
- Fluent English (written and spoken)
- Structured working style
- Proactive working style
- Results-oriented working style
Tasks
- Partner scientifically with the Clinical Project Physician
- Lead or contribute to authoring core trial documents
- Provide scientific input for medical monitoring and data review
- Engage with external clinical experts and organize meetings
- Contribute to regulatory interactions
- Support lifecycle management from early to post-approval stages
- Mentor and provide clinical leadership
- Participate in business development and due diligence activities
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Fluent
Benefits
Competitive Pay
- Competitive salaries
Informal Culture
- Inclusive environment
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
VIATRIS INNOVATION GMBH
Industry
Pharmaceuticals
Description
The company empowers people worldwide to live healthier at every stage of life through access to quality medicines and innovative solutions.
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