Clinical Research Manager
vor 6 Stunden
The Swiss Tropical and Public Health Institute (Swiss TPH) is a world-leading institute in global health with a particular focus on low
- and middle-income countries. Associated with the University of Basel, Swiss TPH combines research, services, and education and training at the local, national and international level. About 850 people from more than 80 nations work at Swiss TPH focusing on infectious and non-communicable diseases, environment, society and health as well as health systems and interventions.
The Clinical Operations Unit is a well-established Clinical Research Service Provider integrated within the Institute. Through our wide network of collaborators, partners and experience, we understand the barriers to delivering clinical trials in difficult settings. We offer strategic, customized and optimized solutions to deliver high quality, high performing clinical trials and meet populations' needs. This is a unique opportunity to join a multicultural, dedicated team, working in a stimulating academic environment with in-depth scientific expertise in the field of poverty related diseases.
In order to reinforce our team, we are seeking a self-motivated, enthusiastic Clinical Research Manager (80-100%).
The key function of this post would be to support the Head of Unit and the unit team in the suc-cessful management of clinical trials.
**Your position**
- Manage (planning, organisation and budget management) small or medium scale clinical studies or act as Deputy of the Project Leader for complex studies
- Manage Clinical Research Associates (CRAs) and Regional Monitors assigned to the study
- Select and train CRAs and Regional Monitors assigned to the study
- Set up and implement monitoring strategies of clinical trials. This includes remote and centralised monitoring if need be
- Plan and conduct pre-selection, site initiation, monitoring and close-out visits and/or re-mote and centralised monitoring activities
- Develop and maintain tools to successfully track initiation, study conduct, monitoring and close out visits of clinical trials
- Preparation of study documentation for ongoing & upcoming clinical trials
- Contribute to clinical trial administration (tracking, filing, etc.)
- Assist site clinical trial staff with study conduct
- Set-up and preparation of budget proposal and budgets
- Actively contribute to the Quality System. This includes facilitating internal audits and contributing to SOPs.
**Your profile**
- Masters in pharmacy, life or medical science specialty or equivalent
- Sound knowledge of ICH-GCP and clinical research
- Minimum of 3 years working at a Lead CRA level and have demonstrated consistently meeting high standards
- Fluent in English and either fluent in French or German, spoken and written
Flexibility & willingness to travel up to 20% to resource limited countries
- Team player with good communication skills
- Precise working style
- Ability to work independently
- Interest in tropical diseases
- Desirable: experience in TB and/or Eastern European countries
**Application / Contact**
- CV
- Motivational letter
- Reference letters and diploma
- Salary expectationsSwiss TPH is an equal opportunity employer committed to excellence through diversity.
**Job Profile**:
Start Date: as soon as possible or upon agreement
Location: Allschwil, Switzerland
Duration: limited to initially 1 year, with possibility of extension
Percentage: 80-100%
Travel Required? Yes, up to 20% to resource limited countries
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