The Clinical Trial Specialist is responsible for the management and clinical execution of assigned clinical trials within Translational Medicine (TM). Functions as the CTL on the planning and implementation of all operational aspects of assigned TM clinical trials from study concept to reporting according to timelines, budget, operational and quality standards (ICH/GCP/SOPs and procedures). The CTS will be assigned studies (scientific and/or operational complexity) including multi-country / multi-center trials. The main focus will be dependent on department workload and need). The person will be responsible for leading and matrix managing the multidisciplinary CTT and support functions to ensure all trial deliverables are met according to timelines, budget, and quality standards.
Firmenprofil
Global Pharma Company
Arbeitsort
Basel
Arbeitsbeginn
Asap
Motivation
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
Ausbildung
BSc or MSc in life sciences or nursing; PhD level scientist with life sciences background
Salärrahmen
As per Industry
Erfahrungen
The candidate should have relevant experience in clinical trial management (e.g. study management in a multi- national environment using different models for trial execution). The candidate should be able to train and support the CRA(s)/CRO(s) on study protocol and related questions and serve as point of contact for managing/answering questions relating to trial procedures and subjects’ eligibility. He/She should be able to author the clinical study protocol and other study essential documents.
Alter
70 CHF/Hr
Sprachen
Englisch: Sehr gut
Spezielles
If you are interested, please send your resume at v.agarwal@universal-job.ch
Vakanz-Nummer
P-13-7164
Global Pharma Company
Basel
BSc or MSc in life sciences or nursing; PhD level scientist with life sciences background
The candidate should have relevant experience in clinical trial management (e.g. study management in a multi- national environment using different models for trial execution). The candidate should be able to train and support the CRA(s)/CRO(s) on study protocol and related questions and serve as point of contact for managing/answering questions relating to trial procedures and subjects’ eligibility. He/She should be able to author the clinical study protocol and other study essential documents.
Chemie
P-13-7164
Temporär
v.agarwal@universal-job.ch