[Hiring] Senior Clinical Project Manager @Ora

Role Description

Ora’s Senior Clinical Project Managers (Sr. CPM) are critical in driving clinical ophthalmic projects forward utilizing best practices in order to ensure budgets, timelines, and clinical trial requirements are being met on behalf of the sponsor. This role will work independently to manage cross functional project teams as well as overseeing other projects they are not directly managing, as a senior member of the clinical operations team, to provide support to more junior team members. Sr. CPM’s have active involvement in each assigned project in order to meet milestones, resolve issues and/or conflicts in addition to frequent interactions with the study team including but not limited to clinical trial associates, monitoring, clinical research coordinators, investigators and senior management. They are responsible for creating project plans and provide weekly budget and progress reviews for each study in addition to preparing high-quality reports.

What You’ll Do

• May manage department Clinical Project Managers, Assistant Project Managers, Clinical Trial Associates and other supporting staff.
• Manages cross functional project teams derived from the groups within clinical development to deliver a high-quality clinical trial(s) in compliance with all regulations and SOPs.
• Works with functional areas on initiating, planning, executing, controlling, closing and resourcing clinical trial projects.
• Acts as an operational nexus or focal point for interdepartmental and intradepartmental groups (e.g. stats, data management, safety, manufacturing, regulatory, vendors).
• Reviews protocol, source documents and CRFs and tracks them to completion.
• Responsible for creating and maintaining project timelines for each project and uses these timelines to track and manage a project’s progress.
• Responsible for creating Project Plans (Roles and Responsibility Tables and Communication Plans) and weekly project budget and progress reviews for each study.
• Reviews study metrics for performance and quality with the team and management.
• Prepares high-quality reports (financial, project, etc.) for management on program status and issues.
• Ensures review of clinical electronic Trial Master File (eTMF) for completeness.
• Manages and coordinates all vendors involved in the clinical trials (e.g. central labs, IVRS, reading centers).
• May represent Ora at professional meetings or seminars.
• Participates in preparing new study budgets, proposal documents and participating in bid defenses.
• Active role in department and company-wide process improvement initiatives.
• Travel of up to 15% is required (mainly domestic, overnight).
• Adhere to all aspects of Ora’s quality system.
• Adhere to all essential systems and processes that are required at Ora to maintain compliance to Ora’s data integrity & business ethics and regulatory requirements.
• Clear and sustained demonstration of Ora’s values -- prioritizing kindness, operational excellence, cultivating joy and scientific rigor.
• Responsibilities may differ from the above based on the specific needs of the business.

Qualifications

• Bachelors’ degree in Life Science with at least 7 years of clinical trial experience. Years of experience may be considered in lieu of education.
• Minimum of 3 years of clinical project management experience.

Requirements

• Ophthalmology experience preferred.
• Understanding of multi-center drug and/or device trials.
• Experience with Veeva TMF and CTMS systems.
• Ability to establish and maintain effective professional relationships with co-workers, managers and clients.
• Highly effective organizational and communication skills.
• Ability to plan, identify risks, anticipate issues and outcomes and respond strategically, tactically and operationally while balancing short-term and long-term company objectives.
• Demonstrated expertise of applicable regulatory requirements and GCP.
• Demonstrated leadership skills and the ability to multitask and to solve problems proactively.
• Proficiency with Excel, PowerPoint and vendor management.
• Multi-lingual communication is a plus.

Benefits

• Competitive salaries along with a structured pension plan.
• Offering private medical insurance healthcare beginning day 1 provided by Vitality and SimplyHealth.
• Company Paid Life & Disability Insurance through Canada Life.
• 25 days of annual leave + Birthday PTO + bank holidays.
• Remote & Wellness Reimbursement for workspace and wellness purchases.
• Continued opportunities to grow and develop your career journey.
• Opportunities to work with colleagues across the globe.
• A chance to research new ophthalmic therapies that will impact patients across the globe.