Clinical Scientist (m/f)

- Preparation, writing and review of clinical study scientific documents such as investigator's brochures, study protocols, study reports, publications, laboratory documentation, ICF, statistical plans
- Search and summarize relevant scientific literature that supports the development of clinical study documents
- Provide necessary scientific support to the CROs / Sites and Clinical Study Team during study execution phase (review of inclusion / exclusion criteria, AE handling, queries on scientific issues etc.)
- Maintenance of up-to-date GCP knowledge and active contribution to continuous improvement in clinical processes
- Active contribution to the medical team activities (e.g, assessment plans, presentations, publications) and interactions with other functions and with external stakeholders / 3rd parties
- Advanced degree (or clinically relevant degree) in life sciences/healthcare is required
- PharmD, PhD preferable
- Fluent English (oral and written)
- Solid, proven technical and operational experience in planning, executing, reporting and publishing clinical studies
- Strong interpersonal skills
- Strong team player
- Ability to deliver in tight timelines
- Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes and clinical development process
- Demonstrates excellent scientific writing skills
- Capability to interpret, discuss and represent study or program level data
- Demonstrates knowledge and application of statistical analysis methodology and can identify trends and interpret / report data effectively

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