IQVIA
Local Trial Manager - Sponsor Dedicated(m/w/x)
Full-timeRemoteSenior
Wien
from 70,100 / year
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BOBoehringer Ingelheim
Regional Clinical Trial Manager(m/w/x)
Wien
from 81,810 / year
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Coordinating international clinical trials, managing data, quality, timelines, and budgets. Project management experience required. Flexible working hours, home office option.
Requirements
- MD or biological/natural science degree
- Prior clinical research experience
- At least 3 years as on-site monitor (CRA)
- Project/trial management experience
- Leadership potential
- Thorough knowledge of international guidelines
- Thorough knowledge of national/regional guidelines
- Thorough knowledge of regulatory topics
- Familiarity with end-to-end clinical trial process
- Collaboration skills
- Ability to work in cross-functional matrix environment
- Ability to prioritize
- Ability to make decisions
- Excellent interpersonal skills
- Excellent communication skills
- Excellent organization skills
- Excellent coordination skills
- Written English proficiency
- Spoken English proficiency
Tasks
- Manage and coordinate international clinical trial preparation
- Execute clinical trial plans
- Manage trial deliverables including data, quality, timelines, and budget
- Establish and maintain relationships with investigators
- Counsel and guide the regional, cross-functional trial team
- Supervise Clinical Research Associates (CRAs) and CRO staff
- Review and submit trial documents and reports to Ethic Committees and Competent Authorities
- Train and lead trial coordinators and CRAs
- Supervise monitoring activities
- Perform Co-Monitoring visits
- Lead and conduct investigator meetings
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Flexible working time models
- Home office
- Flexible working hours
More Vacation Days
- Additional days off
Free or Subsidized Food
- Subsidized staff restaurant
- Vegetarian and vegan options
Learning & Development
- Learning and development opportunities
Healthcare & Fitness
- Health promotion programs
Public Transport Subsidies
- Public transport ticket coverage
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Boehringer Ingelheim 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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BOBoehringer Ingelheim
Regional Clinical Trial Manager(m/w/x)
Wien
from 81,810 / year
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Coordinating international clinical trials, managing data, quality, timelines, and budgets. Project management experience required. Flexible working hours, home office option.
Requirements
- MD or biological/natural science degree
- Prior clinical research experience
- At least 3 years as on-site monitor (CRA)
- Project/trial management experience
- Leadership potential
- Thorough knowledge of international guidelines
- Thorough knowledge of national/regional guidelines
- Thorough knowledge of regulatory topics
- Familiarity with end-to-end clinical trial process
- Collaboration skills
- Ability to work in cross-functional matrix environment
- Ability to prioritize
- Ability to make decisions
- Excellent interpersonal skills
- Excellent communication skills
- Excellent organization skills
- Excellent coordination skills
- Written English proficiency
- Spoken English proficiency
Tasks
- Manage and coordinate international clinical trial preparation
- Execute clinical trial plans
- Manage trial deliverables including data, quality, timelines, and budget
- Establish and maintain relationships with investigators
- Counsel and guide the regional, cross-functional trial team
- Supervise Clinical Research Associates (CRAs) and CRO staff
- Review and submit trial documents and reports to Ethic Committees and Competent Authorities
- Train and lead trial coordinators and CRAs
- Supervise monitoring activities
- Perform Co-Monitoring visits
- Lead and conduct investigator meetings
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Flexible Working
- Flexible working time models
- Home office
- Flexible working hours
More Vacation Days
- Additional days off
Free or Subsidized Food
- Subsidized staff restaurant
- Vegetarian and vegan options
Learning & Development
- Learning and development opportunities
Healthcare & Fitness
- Health promotion programs
Public Transport Subsidies
- Public transport ticket coverage
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Boehringer Ingelheim 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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Boehringer Ingelheim
Industry
Pharmaceuticals
Description
The company is focused on delivering lasting value to patients through innovative therapies and early clinical development.
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