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(Senior) Clinical Trial Associate(m/w/x)
Supporting global clinical trial operations for a plasma protein manufacturer, coordinating logistics and managing eTMF. University degree in a medical-pharmaceutical or scientific field required. Company restaurant, meal subsidy, and health promotion.
Requirements
- Medical-pharmaceutical or scientific university degree
- Previous experience as CTA/Assistant, CRA or similar
- Knowledge of pharmaceutical or CRO industry
- Knowledge of global clinical trials environment
- Solid experience with Phase 2 or 3 studies
- Good IT skills
- Proficient in English (written and oral)
- Additional languages beneficial
- Strong interpersonal communication skills
- Strong organizational skills
- Ability to work efficiently in a team
- Ability to work to tight deadlines
Tasks
- Support global clinical trial operations
- Ensure timely and compliant trial activities
- Coordinate study logistics and documentation
- Update and track trial-related systems
- Maintain study records and (e)TMF management
- Ensure archiving readiness of study documents
- Collaborate with cross-functional teams
- Work with external partners for efficient study conduct
- Identify and escalate operational risks
- Address quality issues and delays
- Contribute to process improvements
- Support training and inspections
- Maintain procedural documents
- Perform additional clinical trial administration tasks
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Free or Subsidized Food
- Company restaurant
- Meal subsidy
Learning & Development
- Training and further education
Healthcare & Fitness
- Health promotion
Parking & Commuter Benefits
- Parking spaces
- Good public transport connections
Team Events
- Company and team events
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(Senior) Clinical Trial Associate(m/w/x)
Supporting global clinical trial operations for a plasma protein manufacturer, coordinating logistics and managing eTMF. University degree in a medical-pharmaceutical or scientific field required. Company restaurant, meal subsidy, and health promotion.
Requirements
- Medical-pharmaceutical or scientific university degree
- Previous experience as CTA/Assistant, CRA or similar
- Knowledge of pharmaceutical or CRO industry
- Knowledge of global clinical trials environment
- Solid experience with Phase 2 or 3 studies
- Good IT skills
- Proficient in English (written and oral)
- Additional languages beneficial
- Strong interpersonal communication skills
- Strong organizational skills
- Ability to work efficiently in a team
- Ability to work to tight deadlines
Tasks
- Support global clinical trial operations
- Ensure timely and compliant trial activities
- Coordinate study logistics and documentation
- Update and track trial-related systems
- Maintain study records and (e)TMF management
- Ensure archiving readiness of study documents
- Collaborate with cross-functional teams
- Work with external partners for efficient study conduct
- Identify and escalate operational risks
- Address quality issues and delays
- Contribute to process improvements
- Support training and inspections
- Maintain procedural documents
- Perform additional clinical trial administration tasks
Work Experience
- 5 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
Benefits
Free or Subsidized Food
- Company restaurant
- Meal subsidy
Learning & Development
- Training and further education
Healthcare & Fitness
- Health promotion
Parking & Commuter Benefits
- Parking spaces
- Good public transport connections
Team Events
- Company and team events
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Octapharma
Industry
Pharmaceuticals
Description
Das Unternehmen ist eines der weltweit größten, das humane Proteine aus menschlichem Plasma und humanen Zelllinien entwickelt und herstellt.
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