This role reports through the Clinical function which provides scientific expertise necessary to design, implement and interpret data from clinical studies.
The role provides scientific input and oversight, as well as leadership and management of cross-functional execution of clinical studies in collaboration with Clinical Operations and Chief Medical Officer.
This role will be responsible for the scientific aspects global clinical trial delivery including protocol design and writing, analysis of data, management and reporting of trials in accordance with company plans/objectives, ICH-GCP, country requirements and company standard operating procedures.
Specifically, this includes writing and/or reviewing protocols, interacting with sites for feasibility assessment, supporting site selection, data review and writing/reviewing the clinical study report, for one or more clinical trials.
Other important tasks will be supporting the Chief Medical Officer and Chief Operating Officer planning, publication strategy and other tasks.

Minimum of a BA/BS in Life Sciences Degree with 7+ years of experience or an advanced clinical/science degree e.g. MA + 5 years of clinical or PharmD/PhD +3 years.
Significant experience working in early and late phase oncology is required to ensure proficiency in knowledge of the disease area(s), KOLs, indication(s), compound(s) under study (including MOA, PK/PD, biomarker & safety profile)
A thorough understanding of the drug development process from pre-IND through registration and post-registration and a broad understanding of functional areas of drug development, including (preclinical, regulatory, pharmacology, translational medicine, pharmacovigilance, data sciences (data management, biostatistics, programming), and clinical operations is required
Strong verbal and written communications skills, including an understanding of medical and scientific terminology and the ability to summarize information effectively
An ability to work collaboratively with team members and stakeholders from different functions.
Proficient in Microsoft Word, Excel, PowerPoint, Electronic Data Capture (e.g., Veeva), J-Review or similar data reporting tools
Adaptable / Flexible
willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism.

Temporary Clinical Scientist

Key skills