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Site Management Associate(m/w/x)
Coordinating clinical trial monitoring activities and ensuring protocol adherence at a global healthcare intelligence organization. Bachelor's degree in life sciences or related field required. Annual leave entitlements, health insurance, and retirement planning.
Requirements
- Bachelor’s degree in life sciences, healthcare administration, or clinical research
- Clinical research, site management, or monitoring experience
- Solid understanding of clinical trial processes and GCP guidelines
- Strong organizational and project management skills
- Ability to handle multiple priorities and deadlines
- Excellent analytical skills and attention to detail
- Focus on maintaining high-quality standards
- Exceptional communication and interpersonal skills
- Ability to build and maintain effective relationships
- Fluent German language skills
- Ability to commute to Munich office 3 times per week
- Encouraged to apply even if not meeting all requirements
Tasks
- Coordinate monitoring activities
- Ensure protocol adherence
- Resolve site-related issues
- Prepare regulatory documents
- Review regulatory documents
- Ensure GCP compliance
- Collaborate with cross-functional teams
- Facilitate effective communication
- Support trial sites
- Track site performance metrics
- Analyze data
- Provide performance reports
- Participate in training
- Mentor junior staff
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
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Site Management Associate(m/w/x)
Coordinating clinical trial monitoring activities and ensuring protocol adherence at a global healthcare intelligence organization. Bachelor's degree in life sciences or related field required. Annual leave entitlements, health insurance, and retirement planning.
Requirements
- Bachelor’s degree in life sciences, healthcare administration, or clinical research
- Clinical research, site management, or monitoring experience
- Solid understanding of clinical trial processes and GCP guidelines
- Strong organizational and project management skills
- Ability to handle multiple priorities and deadlines
- Excellent analytical skills and attention to detail
- Focus on maintaining high-quality standards
- Exceptional communication and interpersonal skills
- Ability to build and maintain effective relationships
- Fluent German language skills
- Ability to commute to Munich office 3 times per week
- Encouraged to apply even if not meeting all requirements
Tasks
- Coordinate monitoring activities
- Ensure protocol adherence
- Resolve site-related issues
- Prepare regulatory documents
- Review regulatory documents
- Ensure GCP compliance
- Collaborate with cross-functional teams
- Facilitate effective communication
- Support trial sites
- Track site performance metrics
- Analyze data
- Provide performance reports
- Participate in training
- Mentor junior staff
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degree
Languages
- German – Fluent
Benefits
More Vacation Days
- Various annual leave entitlements
Healthcare & Fitness
- Health insurance offerings
- Health assessments
Retirement Plans
- Retirement planning offerings
Mental Health Support
- Global Employee Assistance Programme
Other Benefits
- Life assurance
Additional Allowances
- Childcare vouchers
Company Bike
- Bike purchase schemes
Corporate Discounts
- Discounted gym memberships
Public Transport Subsidies
- Subsidised travel passes
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
ICON plc
Industry
Healthcare
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization.
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