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Clinical Trial Assistant - 12 Month Contract
Eingestellt von SEC Recruitment Ltd
Projektbeschreibung
Clinical Trial Assistant/CTA in Switzerland 12 month contract
*Full time
*12 month contract
*Office-based in Switzerland
One of the Global Biopharmaceutical Company is looking for an experienced and ambitious Clinical Trial Assistant to join their organisation in Switzerland.
The primary responsibilities for this role include:
*Collaborate with the Clinical Trial Manager to ensure all operational trial deliverable are met according to timelines, budget, operational procedures and quality standards.
*Management and collaboration with vendors regarding study specific issues.
*Actively contribute to study meeting including meeting minutes and investigator meeting,
*Ensure full compliance (completeness & accuracy) of the required data in study management tools including CTMS, patient enrolment forecasting, etc.
*Contribute to oversight of the required country regulatory (eg CTA, MoH) and country/site IRB/IEC approvals/notifications.
Requirements:
*University Degree or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities
*Fluency in English
*Knowledge of ICH/GCP and regulatory guideline
*Excellent computer skills, proficient in MS Project, Word, Excel, PowerPoint
*Basic understanding of project management including management of budget and vendors.
*Knowledge of drug development process
If you are interested to this opportunity please drop me an email with your updated CV ( (see below) ) or call Camille.
*Full time
*12 month contract
*Office-based in Switzerland
One of the Global Biopharmaceutical Company is looking for an experienced and ambitious Clinical Trial Assistant to join their organisation in Switzerland.
The primary responsibilities for this role include:
*Collaborate with the Clinical Trial Manager to ensure all operational trial deliverable are met according to timelines, budget, operational procedures and quality standards.
*Management and collaboration with vendors regarding study specific issues.
*Actively contribute to study meeting including meeting minutes and investigator meeting,
*Ensure full compliance (completeness & accuracy) of the required data in study management tools including CTMS, patient enrolment forecasting, etc.
*Contribute to oversight of the required country regulatory (eg CTA, MoH) and country/site IRB/IEC approvals/notifications.
Requirements:
*University Degree or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities
*Fluency in English
*Knowledge of ICH/GCP and regulatory guideline
*Excellent computer skills, proficient in MS Project, Word, Excel, PowerPoint
*Basic understanding of project management including management of budget and vendors.
*Knowledge of drug development process
If you are interested to this opportunity please drop me an email with your updated CV ( (see below) ) or call Camille.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges