What are the responsibilities and job description for the Principal Clinical Scientist position at Lifelancer?
Job Title : Principal Clinical Scientist (Office or Remote)
Job Location : Hayward CA USA
Job Location Type : Remote
Job Contract Type : Fulltime
Job Seniority Level : MidSenior level
Description
The Principal Clinical Scientist will be an essential contributor to the scientific clinical and operational scope of clinical development programs with an emphasis on protocolspecific activities. The Principal Clinical Scientist will help drive the design planning and implementation of study protocols for assigned investigational products and will play a key role in supporting related regulatory activities. This role will work on crossfunctional study management teams for the design execution and monitoring of clinical trials as well as assist with data interpretation and communication to both internal and external stakeholders. This individual may also help support internal process improvement initiatives within the clinical department.
Responsibilities
- Partner with crossfunctional teams with potential oversight from senior team members to conduct clinical studies including operational feasibility data management deliverables preparation of meeting materials communication plans safety and medical monitoring data cleaning preparation of status update reports and study closeout activities.
- Support senior team members with medical monitoring reports safety reviews site interactions and reviewing TFLs.
- May be responsible for analytical support of clinical trial data (safety and efficacy) including gathering analyzing reviewing interpreting and providing preliminary assessments and recommendations.
- Analyze information to assess issues relating to protocol conduct and / or individual subject safety.
- Assist in communicating a clear overview of trial results.
- Provide organizational support for Data Monitoring Committees Safety Review Committees or other applicable data review committees including operationalizing the charter preparing updates and data reviews execution of meetings and adjudications and communication of synthesized data reports.
- Author protocols and contribute to authoring of clinical study reports IBs ICFs training documents and other clinical and regulatory documents.
- Interact with internal and external stakeholders (study sites vendors committees etc.) in support of clinical trial objectives; responds to or triages questions for appropriate escalations.
- Act as recognized clinical expert for assigned studies both within and external to Arcus.
- Write and / or review collaborative abstracts posters and content for scientific meetings conferences and publications.
- Support publication strategy execution including collaboration with investigators KOLs medical affairs and other internal / external stakeholders.
- Present at investigator meetings.
- Conduct literature reviews as needed.
Qualifications
Physical Requirements
Must possess mobility to work in a standard office setting and use standard office equipment including a computer; vision to read printed materials and a computer screen; and hearing and speech to communicate in person before groups and over the telephone. This is primarily a sedentary office classification although standing in work areas and walking between work areas may be required. Finger dexterity is needed to access enter and retrieve data using a computer keyboard mouse or calculator and to operate standard office equipment. Positions in this classification occasionally bend stoop kneel reach push and pull drawers open and closed to retrieve and file information. Employees must possess the ability to lift carry push and pull materials and objects weighing up to 25 pounds.
This role can be based at our Brisbane CA location (preferred) or can be remote based. The anticipated salary range for fully qualified candidates applying for this position is $195000 $205000 USD annually. This salary range is an estimate of what we reasonably expect to pay for this posted position. The actual salary may vary based on various factors including without limitation individual education experience tenure skills and abilities internal equity and alignment with market data. In addition to a competitive marketbased salary Arcus offers the opportunity to participate in stock programs a performancebased bonus and a comprehensive benefits package. Additional information about our total rewards program can be found here : .
Arcus Biosciences is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Arcus is committed to the principle of equal employment opportunity for all employees and does not discriminate based on race religion color sex gender identify sexual orientation age nondisqualifying physical or mental disability national origin veteran status or any other legally protected status. EOE / AA / Vets.
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Key Skills
Machine Learning,Python,Data Science,AI,R,Research Experience,Sensors,Drug Discovery,Research & Development,Natural Language Processing,Data Analysis Skills,Toxicology Experience
Employment Type : Full Time
Vacancy : 1
Salary : $195,000 - $205,000