IQVIA
Local Trial Manager - Sponsor Dedicated(m/w/x)
Full-timeRemoteSenior
Wien
from 70,100 / year
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End-to-end protocol implementation and budget management for global therapeutic studies at a clinical research organization with 41,000+ employees. Prior monitoring experience and therapeutic area expertise preferred. Travel up to 20%, global employee assistance program.
Requirements
- Degree in medicine, science, or equivalent
- Ability to drive clinical study deliverables
- Expertise in designated therapeutic area
- Prior monitoring experience preferred
- Ability to travel up to 20%
Tasks
- Plan and manage all clinical trial aspects
- Ensure adherence to timelines and budgets
- Maintain high quality standards
- Collaborate with cross-functional teams
- Establish and implement trial protocols
- Build relationships with investigators and stakeholders
- Ensure compliance with international and local regulations
- Adhere to ethical guidelines
- Make critical decisions on trial design
- Manage vendor selection and risk assessment
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc 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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End-to-end protocol implementation and budget management for global therapeutic studies at a clinical research organization with 41,000+ employees. Prior monitoring experience and therapeutic area expertise preferred. Travel up to 20%, global employee assistance program.
Requirements
- Degree in medicine, science, or equivalent
- Ability to drive clinical study deliverables
- Expertise in designated therapeutic area
- Prior monitoring experience preferred
- Ability to travel up to 20%
Tasks
- Plan and manage all clinical trial aspects
- Ensure adherence to timelines and budgets
- Maintain high quality standards
- Collaborate with cross-functional teams
- Establish and implement trial protocols
- Build relationships with investigators and stakeholders
- Ensure compliance with international and local regulations
- Adhere to ethical guidelines
- Make critical decisions on trial design
- Manage vendor selection and risk assessment
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Childcare
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of ICON plc 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
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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