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Clinical Scientist
vor 3 Wochen
**Clinical Scientist**
We are looking for a clinical scientist with experience in conducting on ongoing trials,
collaboration with the operations team, vendor, site management.The position
supports the overall planning, evaluation and documentation for assigned global
Phase II studies focused on Neuroscience and Rare diseases, in close cooperation
with other functions including Clinical Operations and Medical Directors.
**Responsibilities**:
- Development and writing of study documentation including protocols, informed
consent forms, clinical study reports, as well as clinical science input for study-specific
operational and regulatory documents.
- Responsible for ongoing monitoring of clinical activities and study conduct,
coordination of data collection, data cleaning and review, analysis, and interpretation
as well as preparation and presentation of results for informed decision-making.
- Participate in study management as clinical science representative to ensure trial
deliverables are met according to timelines, budget, quality standards and
operational procedures, within a global multidisciplinary cross-functional Study
Management Team (SMT)
- Provide training and science input to operation colleagues and study site staff, as
agreed with clinical operations.
- Monitor study progress on a regular basis to identify any problems or issues that
could affect the results or completion of the study; you will investigate and employ
problem-solving strategies.
- Collaborate with internal experts, leading academics, and external industry-based
authorities and providers regarding experimental medicine and translational medicine
studies
- Stay at the forefront of scientific and technical excellence by collaborating with the
scientific community, contributing to presenting and publishing high-quality scientific
abstracts, posters, articles and participating in key conferences
Contribute to experimental medicine studies and/or projects in collaboration with
internal or external Partner
**Your profile**:
- Doctoral degree in a relevant scientific field (e.g. Neuroscience, Pharmacology,
Psychology // PhD, Pharma D or MD)
- +5 years in Clinical Science (experience in conducting on ongoing trials,
collaboration with the operations team, vendor, site management)
- Experience in drug development and clinical trials methodology and execution
(Phase 0-2 preferable)
- Familiar with ICH-GCP regulation and regulatory guidance documents about clinical
trials
- Strong project-management skills and ability to prioritize tasks in a dynamic
environment
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