Pae6 - Trainee Clinical Trial Coordinator - 12

Vor 7 Tagen

Lausanne, Schweiz Debiopharm Vollzeit

**_Debiopharm_**_ is an independent biopharmaceutical company based in Switzerland with an ongoing commitment to research in oncology and infectious diseases in order to improve patient outcomes and quality of life. Our main activities include drug development, drug manufacturing and digital health investment. Debiopharm International SA aims to develop innovative therapies that target high unmet medical needs. Our unique “development only” business model allows us to act as a bridge between disruptive discovery products and patient access in international markets. We first identify high-potential compounds for in-licensing, clinically demonstrate their safety and efficacy and then select large pharmaceutical commercialization partners to maximize patient access globally._
- At Debiopharm you will be at the forefront of the fight against cancer and infectious diseases, and you will have the opportunity to work on new innovative medicines for patients. Efficiency is our mode of action, saving lives our collective target._

For our Clinical Operations organization based at our Headquarters in Lausanne, we are looking for a

**Trainee - Pied à l’Etrier - Clinical Trial Coordinator - 12 months**

For our Clinical Operations department based at our Headquarters in Lausanne, we are looking for a Scientific Fellow, Clinical Trial Coordinator (CTC) to support identification of accelerators for clinical trial set up and start up. The Scientific Fellow, Clinical Trial Coordinator (CTC) is involved in the set-up and maintenance of assigned Phase I /II /III clinical trials, and actively supports the Clinical Trial Coordinator (CTC) and the study team in the clinical trial conduct.

**Your responsibilities will be but not limited to**:

- **Identification of clinical trial set up & start up accelerators**
- Identify critical steps of Sponsor related activities during study set up and start up
- Define a method for analyzing performance on past study set up and start up
- Perform analysis for 4 trials, identify trends and recommendations
- **Development of recommendation & Process Improvement**
- Develop tools associated with identified recommendations
- Develop or improve processes associated with these recommendations
- **Recommendation implementation in clinical trials**
- Support the Clinical Trial Coordinator and the Clinical Trial Manager in implementing recommendations for clinical trials in start up
- Under CTC supervision, support the study team in the creation, update, and distribution of study materials, tools and documents.
- Implement and maintain tools associated with identified recommendations
- Assess tool/recommendation effectiveness & facilitate Lessons Learned
- Adjust tools & recommendations according to lessons learned

**Requirements**:
**Your profile**
- Master degree or equivalent in scientific discipline. PhD highly preferred
- Good knowledge of ICH GCP and the drug development regulatory environment
- Language skills: excellent spoken and written English. French is an advantage
- Collaborative skills, ability to coordinate and strong service orientation.
- Strong organizational skills with ability to manage stress, pressure and deadlines.
- Dynamism and pro-activity
- Strong cross-functional communication skills
- Ability to work cross-functionally, to foster a collaborative team environment and to work effectively with others in a matrix organization

**Benefits**

**Debiopharm can offer you**
- Possibility to work from home with weekly visit in the office (Lausanne)
- The opportunity to join a successful company, at the forefront of the most advanced scientific developments in the industry and be exposed to many areas within clinical development and the pharmaceutical industry
- The possibility to be in a company in which innovation, people and entrepreneurship are the fundamentals of its success
- Proud to be an Equal-Pay certified, we ensure offering to all our employees the same opportunities
- Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external staffing agency or recruiter does not create any implied obligation on the part of Debiopharm._

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