Associate 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.

Position Summary:

Reporting to a Sr. Clinical Project Manager of Clinical Operations the Associate Clinical Trial Manager (aCTM) will assist in the implementation and conduct of clinical research projects and provide support for project teams. The position requires knowledge of clinical trial processes and experience in many aspects of trial execution from study start-up to close-out including assisting in the management of clinical vendors or CROs and assisting in the oversight of resources budgets contracts and timelines. The aCTM will also manage the creation organization maintenance and quality of Trial Master File documents and maintain and support the Clinical Trial Master System (CTMS) platform.

Essential Duties and Responsibilities:

• Manage or assist in the management of large global oncology clinical trials (Phase 1-3) ensuring that studies are carried out in accordance with the protocol ICH GCP and local regulatory requirements.
• Support key study-related activities and deliverables.
• Support implementation of training programs ensuring relevant employees are trained as needed to ensure compliance with the protocol and other study-related documents.
• Track study progress and maintain study status updates (e.g. site selection IRB approvals regulatory document collection enrollment SDV status study drug inventory clinical specimen tracking).
• Provide progress updates to relevant project teams and present a plan of action for resolution of issues (e.g. trial issues investigator/study coordinator feedback monitoring issues patient enrollment issues).
• Maintain and support the eTMF and CTMS platform for clinical studies and operational workflows.
• Manage user accounts permissions roles and eTMF/CTMS access.
• Monitor eTMF/CTMS system performance trouble shoot issues and coordinate resolutions with vendor and/or study team members.
• Support eTMF/CTMS system upgrades patches testing and validation activities.
• Maintain TMF structure and index according to ICH-GCP and Erasca SOPs.
• File classify and index documents into the eTMF.
• Perform ongoing review of trial TMF(s) to assure quality and compliance with relevant SOPs and ICH-GCP.
• Track triage and resolve missing or nonconformant documents. Collaborate with study team members to obtain required documents and ensure timely filing.
• Prepare and support regulatory and sponsor inspections/audits (document retrieval audit trails and corrective actions).
• May conduct (co)monitoring visits (pre-study initiation monitoring and closeout) with contracted monitors/CRO.
• Perform all duties in keeping with the Companys core values policies and all applicable regulations.

Required Education and Experience:

• Preference for undergraduate degree in Biological Sciences or professions (pharmacy medicine nursing or other allied health sciences) with a minimum of 1- 2 years of relevant experience.
• At least 1-2 years of experience in 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).
• 1-2 years experience in TMF/document management or clinical trial support.
• Experience with eTMF systems (e.g. Trial Interactive eTMF Veeva Vault).
• Experience with Clinical Trial Master Systems (CTMS) (e.g. Trial Interactive CTMS Medidata CTMS) preferred.
• Demonstrated track record of successfully supporting multiple projects trials and priorities.
• Experience with managing study vendors (e.g. CRO IRT/IXRS central laboratories eTMF/CTMS) preferred.
• Practical knowledge and implementation of ICH-GCP guidelines and US and ex-US regulations.
• Ability to work well with global multi-disciplinary teams.
• Must be a self-starter able to thrive in an entrepreneurial fast paced and dynamic work environment.
• Must be organized with excellent oral and written communication skills.
• Strong learning orientation curiosity and commitment to science and patients.

The anticipated salary range for this position is $122000 to $137000.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.