Sr Clinical Scientist (contract)
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Job Location:
San Diego, CA - USA
Monthly Salary:
Not Disclosed
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
Erascais a clinical-stage precision oncology company focused on discovering developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancersmost commonly mutated signaling cascades the RAS/MAPK pathway which affects approximately 5.5 million lives each year worldwide. The name Erasca has an important embedded meaning: it is a contraction of our audacious hope to erase cancer that drives our mission and everything that we do on behalf of patients with cancer.
PositionSummary:
The contract Sr Clinical Scientist will support the clinical aspects of one or more clinical studies and will work closely with cross-functional teams to ensure the successful execution and completion of clinical trials. This is a 12-month contract renewable and will require 20-30 hours per week. Some flexibility with working hours will be essential to respond to sites.
Essential Duties and Responsibilities:
- Key clinical deliverables include:
- timely screening of patient enrollment packages from sites
- addressing site inquiries
- data review and cleaning
- medical and scientific input into the development of deliverables required for study activation and conduct (CRFs SAP data listings etc.)
- document development (INDs Protocols IBs applicable regulatory documents etc.)
- other support and deliverables as needed
- In collaboration with other functions and stakeholders develop responses to Health Authorities and IRBs on clinical or medical questions.
- Perform all duties in keeping with the Companys core values policies and all applicable regulations.
Required Education and Experience:
- Undergraduate degree required; PhD PharmD or other relevant advanced degree in a health science field preferred.
- At least 10 years of biotech or pharmaceutical industry experience as a clinical scientist or in a closely related clinical development function.
- Experience in oncology clinical trials required early development experience a plus.
- Demonstrated ability to evaluate interpret and present complex scientific data.
- Knowledge of biostatistics GCP and regulatory requirements for clinical studies; extensive experience with data analysis and interpretation; understanding of principles of safety and pharmacovigilance.
- Strong verbal and written communication and presentation skills.
- This person must be flexible responsive and self-sufficient.
- Demonstrated ability to meet deadlines in a fast-paced environment; a collaborative team player with a can-do attitude and the ability to identify and implement creative solutions to complex problems.
Along with our casual collaborative and fun work and the chance to make your mark in our mission to erase cancer Erasca offers a comprehensive and competitive benefits package that includes: Paid Time Off Holiday and Sick Leave Medical Dental and Vision Plans Short- and Long-Term Disability Basic and Voluntary Life/AD&D Coverage Flexible Spending Accounts (FSA HSA and Commute) Critical Illness and Accident Coverage Pet Insurance Employee Assistance Program 401(k) Plan with Erasca contribution and the opportunity to participate in an Employee Stock Purchase Program.
Erasca Inc. is an Equal Opportunity Employer and takes pride in maintaining a diverse and inclusive environment. We do not discriminate in recruitment hiring training promotion or other employment practices for reasons of sex race religion national origin ancestry physical or mental disability protected medical condition genetic information marital status registered domestic partner status age sexual orientation military and veteran status or any other basis protected by federal state or local law or ordinance or regulation.
Required Experience:
Senior IC
Key Skills
About Company
Erasca is a clinical-stage precision oncology company driven by a bold mission—to erase cancer. We are on a journey to shut down one of cancer’s most commonly mutated signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide. Our promi ... View more
