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Clinical Trial Associate - One Year Contract - Switzerland
Eingestellt von SEC Recruitment Ltd
Gesuchte Skills: Support
Projektbeschreibung
A Global Biopharmaceutical Company committed to patient support is urgently looking for an experienced Clinical Trial Associate for a one year contract in Switzerland.
In collaboration with the Clinical Trial Manager, you will contribute to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/WPs.
Keys information:
*Full time
*12 month contract
*Office-based in Switzerland
The primary responsibilities for this role include:
*Management and maintenance of study deliverables in collaboration with internal and external stakeholders.
*Lead/Participate in monitoring visit report and coordinate study training for study team.
*Risk identification and implementation of actions to avoid it.
*Collaborate closely with vendor.
*Actively contribute to study meeting including meeting minutes and investigator meeting,
*Manage TMF set-up, ongoing quality review, and final reconciliation
*Assist the Clinical Trial Manager with maintenance of study budget.
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
*Demonstrates analytical approach and anticipation of problems
*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) ) and/or call Camille
In collaboration with the Clinical Trial Manager, you will contribute to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/WPs.
Keys information:
*Full time
*12 month contract
*Office-based in Switzerland
The primary responsibilities for this role include:
*Management and maintenance of study deliverables in collaboration with internal and external stakeholders.
*Lead/Participate in monitoring visit report and coordinate study training for study team.
*Risk identification and implementation of actions to avoid it.
*Collaborate closely with vendor.
*Actively contribute to study meeting including meeting minutes and investigator meeting,
*Manage TMF set-up, ongoing quality review, and final reconciliation
*Assist the Clinical Trial Manager with maintenance of study budget.
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
*Demonstrates analytical approach and anticipation of problems
*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) ) and/or call Camille
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Sonstiges