Clinical Research Scientist
1 week ago
Our mission is to Profoundly change the standard of care by creating a tomorrow where clinicians can confidently ablate tissue with precision; a tomorrow where patients have access to safe and effective treatment options, so they can quickly return to their daily lives. Changing the standard of care is part of our fabric. We are a group of energetic, problem-solvers focused on innovation, and looking to change the world. We are changing the paradigm for treating diseases such as prostate cancer by using real-time MR Imaging, thermal ultrasound and close-loop temperature feedback control, to gently ablate the diseased tissue with mínimal side effects.
If you share our values and want to work in a collaborative results focused culture and want to make a Profound impact in healthcare and your career, here is your chance.
**The position is available on a 12-month contract basis with the possibility of transitioning to be a permanent role.**
**General Accountability**:
The Clinical Research Scientist is accountable for a range of responsibilities related to clinical trial recruitment and data analysis. In addition, s/he is primarily responsible for preparing manuscripts for publication based on the findings of the clinical trials. These tasks require to collaborate effectively with cross-functional teams and ensure that all activities are completed accurately and within the timelines provided.
**Duties and Responsibilities**:
- Contribute to and execute the publication strategy for utilization and reimbursement
- Extract, analyze, interpret, and visualize clinical data, developing code as necessary to facilitate these tasks
- Develop analytics to track patient flow in the clinical trials pipeline
- Communicate clinical and technical data for sponsored studies and regulatory filings
- Prepare presentations, manuscripts, abstract and reports and conduct scientific literature searches, data summaries, and systematic reviews as needed
- Execute on the strategy for site engagement to support timely clinical trial recruitment
- Perform quality control for clinical data to ensure accuracy, completeness, and verifiability from source documents, and resolve any discrepancies using query process
- Verify the accuracy of Adverse Event reporting and ensure that it adheres to GCP guidelines and applicable regulatory requirements
- Advise marketing team on TULSA market positioning, and produce competitive assessment reports and briefings as needed
- Fulfill other duties as required to support the Clinical Science team
**Education and Certification**:
- Degree in the field of life sciences, biostatistics, or a related discipline.
- Master’s or PhD degree in science or engineering is strong preferred
**Key Attributes (experience, skills and technical knowledge)**:
- 2 -5 years of experience in clinical research or a related field
- Exceptional analytical skills with strong attention to detail, enabling accurate and precise interpretation of complete data sets.
- Exceptional oral and written communication skills, to effectively convey scientific and technical information
- Knowledge of biostatistical methods and systematic literature reviews
- Strong initiative and problem-solving skills, with the ability to identify issues and proactively develop and implement effective solutions
- Focused and self-motivated and able to work with limited supervision
- Proficiency in Microsoft Office, Visual Basic and R Statistical Software.
- Knowledge of Good Clinical Practice (GCP) guidelines is an asset.
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