Associate Study Manager (SLV/MST)
- Experience Level
- Experienced (non-manager)
For one of our client, a multinational biopharmaceutical company located in North Switzerland, we are looking for an Associate (Clinical) Study Manager for a permanent position. In this role, you will be responsible to ensure that clinical trials are completed on time, within budget and in compliance with the protocol, ICH/GCP and applicable regulatory requirements. You will have to maintain a high level of professionalism within the company and in interactions with external stakeholders.
If you are a motivated, eager-to-learn and passionate young professional, you are the right person for this job!
- Co-monitoring investigative sites to ensure protocol compliance, field monitor performance and appropriate study conduce;
- Reviewing monitoring visit reports and track all items to resolution;
- Supporting and interacting with CROs, vendors and study sites as needed to respond to issues;
- Assisting in preparation of study specific documents, reports and materials as appropriate;
- Cooperating with the team as appropriate in the preparation of regulatory documents and submissions;
- Participating in the review of CRF and clinical database listings for completeness and accuracy;
- Planning investigator and other relevant meetings;
- Coordinating and reviewing regulatory documents from study sites, to ensure completeness and accuracy;
- Developing knowledge of the investigator contract, budget and payment process;
- Flexibility necessary for travelling and working hours/working schedule.
- University Degree or equivalent required in a scientific field;
- At least 2 years Pharma-related/clinical research related experience;
- Previous experience as Senior/Lead Clinical Research Associate or site monitor at global level;
- Relevant working/residency permit or Swiss/EU-Citizenship.
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