Clinical Trial ManagerSr Clinical Trial Manager

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.

The Clinical Trial Manager or Senior Clinical Trial Manager assists in the planning implementation and management of clinical studies from concept to completion. The position requires knowledge of clinical trial processes and prior experience in many aspects of trial execution from study start-up to study close-out including assisting in the management of clinical vendors/CROs and assisting in the oversight of resources budgets contracts and timelines.

Essential Duties and Responsibilities:

• Manage global clinical trials (Phase 1-3) in oncology indications ensuring that studies are carried out in accordance with the clinical development plan ICH-GCP and FDA/other regulatory agency requirements.
• Recruit global study sites and foster relationships with study investigators.
• Participate in the process of site and vendor selection qualification and activation.
• Develop Requests-for-Proposals and assist in vendor selection efforts.
• Assist in review and negotiation of vendor contracts and study site clinical trial agreements.
• Manage study vendors (e.g. CRO IRT laboratories core ECG/imaging).
• Monitor the progress of trials including enrollment and clinical trial material inventory.
• Review monitoring visit reports for completeness and adherence to the annotations.
• Assist in packaging/labeling/distribution of clinical trial material.
• Monitor and track biological samples for applicable analyses.
• Provide progress updates to management and during program team meetings.
• Assist in departmental budgeting including accruals and projections.
• Assist in development of protocols consent forms IRB/EC materials and other trial documents.
• Assist in development of Clinical SOPs.
• Prepare/review/approve study materials such as CRFs patient diaries drug accountability forms study and investigator manuals project plans and monitoring reports.
• Assist in electronic case report form design and development.
• Assist in IRT design and development.
• Participate in data cleaning activities and developing appropriate data outputs.
• Understand and help fulfill the needs of other Erasca departments (e.g. Finance Research).
• Provide leadership and mentoring of other Clinical team members.
• Perform all duties in keeping with the Companys core values policies and all applicable regulations.

Required Education Experience and Attributes:

• Preferred undergraduate degree in life sciences or professions (pharmacy medicine nursing or other allied health sciences).
• For Clinical Trial Manager at least 5 years of relevant experience in oncology clinical operations in pharmaceutical company or CRO including trial set-up monitoring and close-out of US and non-US trials at all phases of pre-NDA clinical research (Phases 1-3). For Senior Clinical Trial Manager at least 7 years of relevant experience required.
• Demonstrated excellence in trial management skills with track record of successfully managing multiple projects trials and priorities.
• Experience with managing study vendors (e.g. CRO IRT laboratories core ECG/imaging).
• Ability to work well with global multi-disciplinary teams.
• Experience in practical knowledge and implementation of ICH-GCP guidelines and US and ex-US regulations.
• Experience with electronic data capture and data management software.
• Experience in the management of Clinical Research Associates.
• Excellent oral and written communication skills.
• Experience with reviewing monitoring trip reports
• Must be able to thrive in an entrepreneurial fast-paced and dynamic work environment.
• Must be organized and be able to communicate effectively.
• Must be a self-starter.
• Strong learning orientation curiosity and commitment to science and patients.

The anticipated salary range for this position is $145000 to $190000.The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job type and length of experience within the industry education etcetera. In addition to base salary the hired applicant will be eligible to receive an annual bonus and an equity grant at hire and annually in the form of the option to purchase stock in the future for a specified price.

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.