Company Description

ORIC is a research-driven company dedicated to discovering and developing novel therapies that can Overcome Resistance In Cancer. Our collaborative, empowering culture gives scientists authority, responsibility, and support to do cutting-edge work on therapies for treatment-resistant cancers. Our culture and values support our mission, provide a shared understanding of how we work together as a company and provide a clear sense of what is most important to us as an organization.

We are looking for a Senior Clinical Trail manager who will plan, implement and manage clinical studies from concept to completion. Participate in project teams as the study lead or as an active member. Manage clinical vendors and CROs, including budgets, contracts, and timelines. This is a hybrid position with an expectation of being onsite a minimum of two days per week.

Job Description

Essential duties and responsibilities include the following. Other duties may be assigned.

• Assist in management of global oncology clinical trials (Phase 1-3), ensuring that studies are carried out in accordance with the clinical development plan, GCPs, ICH and FDA requirements

• Participate in the process of site and vendor identification, selection and qualification

• Assist in regulatory document collection and review

• Manage study vendors (e.g., CRO, IRT/IXRS, laboratories)

• Monitor the progress of trials including enrollment and clinical trial material inventory

• Provide progress updates to management, develop protocols, consent forms, IRB/EC materials, and other trial documents

• Assist/lead in developing procedural plans

• Review and identify trends in enrollment and data entry at sites and proactively interface with CRO’s clinical monitoring team

• Verify monthly accruals from vendors and study sites

• Assist in case report form (CRF) development and programming of electronic data capture

• Support project review specifications for IRT/IXRS and other vendors

• Assist in data cleaning and database lock

• Prepare or review and approve study materials such as CRFs, patient diaries, drug accountability forms, study and investigator manuals, monitoring plans, and monitoring trip reports.

• Provide study updates at clinical operations meetings-including updating other clinical staff and upper management on patient recruitment, trial issues, investigator’s feedback, monitoring issues, patient enrollment issues and presenting a plan of action for resolution of issues

• Perform all duties in keeping with the Company’s core values, policies and all applicable regulations

Qualifications

• BA/BS with science major, or an equivalent combination of education and related experience

• At least 8 years of relevant oncology experience in clinical operations in pharmaceutical/biotechnology 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)

• Must be able to thrive in an entrepreneurial, fast-paced, and dynamic work environment

• Must be organized and be able to communicate effectively

• 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/IXRS, laboratories)

Additional Information

The anticipated salary range for candidates who will work in our San Diego location is between $160,000-$190,000 for a senior clinical trial manager. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the title, type and length of experience within the job, type and length of experience within the industry, education, etc.

ORIC Pharmaceuticals, Inc. is an equal opportunity employer. ORIC does not discriminate based on race, color, religion, gender, sexual orientation, gender identity, age, national origin, disability status, protected veteran status, or any other legally protected characteristics.