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Clinical Trial Associate
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Support, Client
Projektbeschreibung
You're an outstanding professional with experience in the pharmaceutical area? Your profession is your passion? You're a problem solver who is looking for a new challenge? Great!
Our client, an international pharmaceutical company, is looking for you!
As Clinical Trial Associate you assist in the operational and logistical aspects of clinical trials according to ICH-GCP and internal procedures. You also assist in delegated tasks to support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study
As well you are responsible for:
- Providing support to the Clinical Trial Leader (CTL) with many of the tasks involved with the smooth running of clinical trials in compliance with internal processes. You collaborate with the CTL in taking action to address issues as they arise
- Helping manage clinical, regulatory and study-related essential documents such as study protocols, Case Report Forms, Informed Consent Forms etc.; reviewing documents for completeness, accuracy and compliance with protocol and appropriate regulations. Identifying issues and taking appropriate corrective action as necessary.
- Liaising with contract organisations, vendors and other suppliers of project support services to ensure study deliverables are met eg contribute to documentation, processes and set-up activities to facilitate efficient working and effective partnerships with external groups.
- For setting up and maintaining Trial Master Files and ensuring all relevant study documents are filed and archived based on the appropriate guidelines in collaboration with the Trial Document Specialist.
- Auditing existing Paper Trial Master Files, collecting outstanding documents and archive after study is completed
Ideal Background:
- A bachelor's degree or equivalent qualification or work experience in life sciences or nursing
- Experience in working with Trial Master Files
- Previous experience in clinical trials (eg clinical trial design, execution and operations) is preferred but not required
- Good organizational and interpersonal skills
- Ability to work in a team as well as independently if required and to manage multiple priorities with support
- Computer literate
- Fluent in English oral and written
We offer you a competitive salary and an interesting challenge in a well named company which will benefit your career.
If you are the person we're looking for please submit your application. We're looking forward to getting to know you.
Our client, an international pharmaceutical company, is looking for you!
As Clinical Trial Associate you assist in the operational and logistical aspects of clinical trials according to ICH-GCP and internal procedures. You also assist in delegated tasks to support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study
As well you are responsible for:
- Providing support to the Clinical Trial Leader (CTL) with many of the tasks involved with the smooth running of clinical trials in compliance with internal processes. You collaborate with the CTL in taking action to address issues as they arise
- Helping manage clinical, regulatory and study-related essential documents such as study protocols, Case Report Forms, Informed Consent Forms etc.; reviewing documents for completeness, accuracy and compliance with protocol and appropriate regulations. Identifying issues and taking appropriate corrective action as necessary.
- Liaising with contract organisations, vendors and other suppliers of project support services to ensure study deliverables are met eg contribute to documentation, processes and set-up activities to facilitate efficient working and effective partnerships with external groups.
- For setting up and maintaining Trial Master Files and ensuring all relevant study documents are filed and archived based on the appropriate guidelines in collaboration with the Trial Document Specialist.
- Auditing existing Paper Trial Master Files, collecting outstanding documents and archive after study is completed
Ideal Background:
- A bachelor's degree or equivalent qualification or work experience in life sciences or nursing
- Experience in working with Trial Master Files
- Previous experience in clinical trials (eg clinical trial design, execution and operations) is preferred but not required
- Good organizational and interpersonal skills
- Ability to work in a team as well as independently if required and to manage multiple priorities with support
- Computer literate
- Fluent in English oral and written
We offer you a competitive salary and an interesting challenge in a well named company which will benefit your career.
If you are the person we're looking for please submit your application. We're looking forward to getting to know you.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Sonstiges