Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers. Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission. Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust. By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients. It’s our work, our passion, and our legacy. We invite you to join us.
Hybrid
Employee Value Proposition:
At Taiho Oncology, the compassion we practice for our patients extends to our team, empowering and motivating them to do their best work for those who need it most. This is an exciting opportunity to lead clinical studies and experience multiple facets of Clinical Operations in a dynamic, supportive, collaborative and global cross-functional environment.
Position Summary:
Under minimal supervision, leads and manages multiple complex global studies to support the Clinical Development Plan. The Associate Director (AD) is responsible for ensuring assigned clinical studies are delivered within timelines, budget, and quality. A critical component of the position is leading, collaborating with and driving internal cross-functional study teams and managing, contract research organization (CRO) personnel and other study vendors. Performs assigned responsibilities to ensure timely completion of departmental goals and objectives. The AD may represent the department on compound level teams to support the compound development plan and ensure its execution.
Performance Objectives:
Assumes overall responsibility for the planning and execution of one complex Ph3 study or multiple global trials by managing all aspects of trial deliverables, including development of timelines, budget, recruitment and country/site selection strategies, and provision of clinical trial materials.
Serves as main study contact for the cross functional team, CROs, vendors and study sites.
Monitors KPI and performance metrics and drives related discussions and escalations with the cross functional study teams and CROs/vendors. Escalates risks/issues and reports status to clinical operation lead.
Participates in the preparation of protocols and Case Report Forms (eCRFs), data management, monitoring, communication, and other project plans.
Authors and leads the coordination of study specific documents such as Informed Consent.
Works with CROs to develop processes and mitigation strategies for assigned studies.
Collaborates with Clinical Development and CRO on study-specific training for study team and study sites.
Responsible for the financial management of the clinical trial in conjunction with his/her supervisor and finance department, including contracts, change orders and invoices.
Efficiently establishes and monitors trial milestones as well as overall day-to-day operations of clinical studies, ensuring study information and timelines are accurate in internal electronic systems, reports and on government websites (CT.gov, etc).
Ensures the timely recruitment of trial participants with secure randomization processes, if applicable, and subsequent efficient and effective data management.
Ensures compliance with and adherence to the project plan and identifies, evaluates and mitigates potential risks and issues.
Oversees systems to track projects including all study, investigator and ethical review board information, patient recruitment activity, and financial management.
Liaises with the Trials Steering Committee, Data Monitoring, and Ethics Committee as required.
Provides regular and ad hoc information, both written and verbal, to all the trial participants, internal/external teams including reports, updates, guidance, preformed commitments, etc.
If required, conduct co-monitoring visits with CROs or CRAs.
Leads site identification and selection process in collaboration with internal Medical lead and CROs to ensure suitability of study sites. Verifies that all research staff and facilities have adequate qualifications and resources and these remain adequate throughout the study.
Ensures that study sites are set up properly and each has the trial materials, investigational products, and training according to trial specific requirements and industry standards.
Verifies that the investigator follows the approved protocol, training and all GCP procedures and oversees the quality of the data and safety of the patients. Communicates deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements to internal management and the investigator, as applicable.
Provides proper oversight of study CROs and vendor activities by creating and managing the CRO oversight plan and related activities, such as review of various monitoring visits report and follows up on any issues or trends, managing risk/issue/decision logs, etc.
Ensures data is entered and monitored in timely manner and that safety is reported in accordance with the protocol on the CRFs.
Works with internal and external functional teams to ensure drug accountability is managed at study sites and that all used and unused trial supplies are accounted for. Ensures IP release process is followed and associated documentation is complete.
Manages sites and study closeout related activities and trial completion.
Overall responsible for the Trial Master File, including review of the TMF plan, related metrics, and ongoing quality review of the TMF. Oversees TMF related CRO and internal team activities to ensure inspection readiness of trial documentation.
Supports Quality on site audits, CAPA and inspection requests.
Manages and coordinates investigator meetings and internal/external team cross functional study meetings and related agenda/minutes.
Interacts and communicates with Taiho’s partners for both planning and operational execution of day to day activities.
Leads selection, setup and provides oversight to various study vendors such as IRT, ePRO, ECG, Central lab, etc.
Provides support, mentorship, and training for others in Clinical Operations.
Leads various projects such as SOP development or process improvement initiatives.
Acts as a liaison for clinical study activities with parent company in Japan.
Represents Clinical Operations on global product level teams to support clinical development plan strategy and provides timelines and budget scenarios to support team at governance.
Provide training and mentorship to other in Clinical Operations, as needed
Education/Certification Requirements:
Bachelors’ degree in in the biological sciences or equivalent is required.
Knowledge, Skills, and Abilities:
Minimum 5 years of clinical operation trial management experience in the pharmaceutical, biotechnology, CRO and/or healthcare industry
3+ years of managing and leading Ph 3 or complex Ph 2 global trials experience preferred
Has demonstrated the use of excellent communication skills, command of medical terminology and of the application of scientific/medical and clinical concepts used to conduct Phase I-IV clinical trials.
Attention to details and well-organized.
Ability to work independently with minimal management oversight
Solution oriented and exceptional collaboration skills.
Must possess the ability to multi-task and effectively prioritize in order to ensure clinical trial goals.
Recognize potential obstacles and work to resolve them within set timelines.
Delivers work conscientiously and precisely even when under pressure
A team player and able to work in a dynamic, fast-paced environment with attention to high quality results.
Excellent communication skills both verbal and written.
Good proofreading skills.
Takes initiative and utilizes good judgment
Knowledge of, and competence in, application of FDA/GCP/ICH guidelines.
The pay range for this position at commencement of employment is expected to be between $178,500 - $210,000 annually; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as PTO, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.
If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
