Clinical Trial Manager/Sr Clinical Trial Manager

Essential Duties and Responsibilities

• Manage global clinical trials (Phase 1-3) in oncology indications, ensuring compliance with clinical development plans, 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.
• Absorb and negotiate vendor contracts and study site clinical trial agreements.
• Manage study vendors (e.g., CRO, IRT, laboratories, core ECG/imaging).
• Maintain progress of trials, including enrollment and clinical trial material inventory.
• Review monitoring visit reports for completeness and adherence to annotations.
• Assist in packaging/labeling/distribution of clinical trial material.
• Maintain and track biological samples for applicable analyses.
• Provide progress updates to management and during program team meetings.
• Absorb departmental budgeting, including accruals and projections.
• Absorb the development of protocols, consent forms, IRB/EC materials, and other trial documents.
• Absorb the development of Clinical SOPs.
• Absorb the preparation/review/approval of study materials such as CRFs, patient diaries, drug accountability forms, study and investigator manuals, project plans, and monitoring reports.
• Absorb the electronic case report form design and development.
• Absorb the IRT design and development.
• Absorb 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 Company's 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.

Pay

The anticipated salary range for this position is $145,000 to $190,000. 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.

Benefits

• 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
• Opportunity to participate in an Employee Stock Purchase Program

About the Role

Erasca is 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 cancer's most 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.

Qualifications

None provided in the job posting.

Skills

None provided in the job posting.

Benefits

None provided in the job posting.

Schedule

None provided in the job posting.