Associate Director/Director, Clinical Operations

Description Tris Pharma, Inc. ( is a leading privately-owned US biopharmaceutical company focused on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs. We have >150 US and International patents and market several branded ADHD products in the US. We also license our products in the US and ex-US markets. Our robust pipeline of innovative products employing our proprietary science and technology spans neuroscience and other therapeutic categories. Our science and technology make us unique, but our team members set us apart; they're the engine fueling Tris' passion and innovation. Our colleagues understand the criticality of operating a successful business and take pride in the company's success. Equally important is how we interact on a daily basis. We believe in each other and in respectful, open and honest communication to help support individual and team success. We have an immediate opening in our Monmouth Junction, NJ facility for an Associate Director or Director, Clinical Operations. Title and level commensurate with experience. The Associate Director/Director, Clinical Operations is accountable for overseeing and directing the planning, execution and daily operations of an individual company study or portfolio of studies, as well as managing cross-functional teams to ensure delivery in accordance with established timelines, budget, and quality standards. The incumbent provides direction and guidance to Clinical Operations team members and develops program/study operational strategies including, but not limited to scenario models for optimal delivery linked to value drivers and implications for time, quality, risk and budget Responsibilities Oversees operational delivery of one or more complex programs or studies, ensuring program/study deliverables and milestones are met with quality, timeliness and within budget; Serves as key operational point of contact for assigned programs/studies for portfolio leaders; Participates in program strategy meetings and contributes to the operational strategy for assigned programs/studies Leads and collaborates with cross-functional teams to oversee performance of activities required to deliver programs/studies on time; Creates strong strategic partnerships with cross-functional colleagues ensuring consistent approaches to program/study delivery, data collection and reporting across programs Provides direction and support to Clinical Operations team members and develops program/study operational strategies including, but not limited to: scenario models for optimal delivery linked to value drivers and implications for time, quality, risk and budget Reviews and provides expert Clinical Operations input into clinical documents related to the drug development process including study synopsis and protocols, clinical study reports and all project plans Provides regular executive updates to senior management; Oversees delivery quality, ensures inspection readiness and interacts regularly with program/study team members regarding issues, risks and successes related to study delivery Supports study budget negotiations and manages Clinical Operations spending related to study execution; Works closely with Outsourcing Management, Finance and Clinical Operations Leadership to ensure budgets are accurate Participates actively in external service provider selection, including Contract Research Organizations (CROs) and other vendors, as necessary; Ensures appropriate CROs and vendors are identified, vetted and managed throughout the life of the study Works with internal and external teams, as required ensuring programs are initiated and managed in line with company strategy and key clinical and regulatory milestones; Proactively identifies and communicates program/study issues that may impact budget, resources and timelines; escalates, as appropriate Participates in vendor governance committees, as appropriate Leads and/or contributes to department initiatives and assists in the design and implementation of standardized work processes Provides expert and collegiate support to other members of the drug development team to ensure full success of company's portfolio and regulatory milestones Assists in Standard Operating Procedures (SOPs) and working instruction development, review and approval Performs sponsor oversight of monitoring visits, including site qualification, study site initiation, routine monitoring and study site closure visits, including review of monitoring reports and follow-up letters Oversees and manages CRA teams and/or Clinical Trial Assistants, as applicable Requirements Qualifications: Bachelors degree in a scientific or health care field and minimum 7 years clinical development and/or operation experience, including majority of time in clinical study/project management in positions of increasing technical and leadership responsibility in the pharmaceutical, biotechnology, CRO or related industry. Current, hands on experience working in early phase clinical studies/Phase I-III studies Experience supervising or overseeing CROs and other clinical trial related vendors, #J-18808-Ljbffr Tris Pharma, Inc.