What are the responsibilities and job description for the Clinical Development Scientist position at Phanesthera?
Position : Clinical Development Scientist
Read the overview of this opportunity to understand what skills, including and relevant soft skills and software package proficiencies, are required.
Function : Clinical Development and Operations
Company : Phanes Therapeutics, Inc.
Phanes Therapeutics is a clinical stage biotech company focused on innovative discovery research and clinical development in oncology. We are looking for motivated and passionate people to join us to help discover and develop new medicines and improve healthcare. Our mission is to become a major source of innovation in the biotech and pharma industry.
Job Summary :
The position is on-site full time in the clinical development team located at our R&D site in San Diego, CA. The candidate should have solid training and / or broad experience in a scientific discipline. Under the supervision of the Clinical Development Director, the candidate will provide scientific support in all aspects of the clinical programs, such as literature review, scientific writing, data analysis, presentation, and summary. This candidate will be a resource to teams for guidance of matters related to analysis and communication of clinical data.
Key Responsibilities :
- Clinical Strategy :
- Integrate scientific knowledge and clinical data, in adherence with the Clinical Development Plan, to ensure translation of clinical research plans into high quality studies.
- Provide clinical support and scientific opinion to study teams.
- Provide input on clinical trial documents, milestones and timelines.
- Maintain scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment.
- Data Analysis :
- Analyze, review, and curate key clinical trial data in a timely manner.
- Organize and manage key clinical trial data.
- Presentation and Documentation :
- Review, analyze, evaluate and interpret results of clinical trial data for internal and external presentation.
- Involve in the development of clinical research protocols and regulatory submission documents.
Qualifications :
Our Benefits Include :
The annual base salary we reasonably expect to pay is $110,000.00 - $170,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties / requirements, and relevant experience and skills.
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Salary : $110,000 - $170,000