Clinical Trial Manager

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer.OverviewThe Clinical Trial Manager has operations experience within the biotech/biopharma arena. This individual has a high level of core competencies and technical skills to be applied within the management of clinical programs leading to registrational submissions of Biologic License Applications (BLAs).The Clinical Trial Manager position is an opportunity for an individual to join a cross-functional clinical team having high-visible and dynamic input in a therapeutic indication of unmet medical need and orphan disease status.Essential Functions and ResponsibilitiesSupport the overall operational execution of clinical studies on one or more clinical programs from initial study synopsis through final project deliverables (ie, database hard-lock, final TLFs, CSR, etc.)Manage the implementation, on-time execution and conduct of clinical studies; including the development of budget items, milestones and timelines, in addition to scope and management of resources (including vendor selection). All leading to overall quality, safety, and compliance throughout the duration of the clinical studies and program.Oversight of cross-functional study team members to ensure initiation and execution of the clinical program within approved budget and timelinesRisk management and mitigation including prioritization of competing tasks and issues to ensure program/study objectives are successfully accomplished.Lead role in vendor identification/qualification/selection, systems set-up/management including EDC, IWRS, Central Laboratories, specialty services (ePRO, eDiary, etc.)Understanding of how to support and deliver the trial endgame, which is the data and statistical analysesCritically assess data to detect trends and outliers to efficiently direct resources and attention to correct problems earlyAbility to critically review and supervise a multifunctional vendor groups including clinical operations, data management and biometricsEnsure data integrity through routine data reviews, query and resolution, consistency checks both internally and for independent DMC/DSCEffectively tracks and communicate program/study progress to Senior Management with ability to create and update detailed dashboards and trackersAwareness of competitive landscape, changing regulations and guidance with ability to assess the impact on clinical projects and make modifications as necessaryAbility to creatively approach challenges and problem resolution to optimize the conduct of clinical trialsMust adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.Perform miscellaneous duties as assigned. Required Education, Skills, and KnowledgeBachelor’s degree with 5+ years of pharmaceutical or biotech-related/clinical research, oncology or research experience and at least 1 year as CTMDemonstrated experience in core and technical aspects of designing, initiating and managing phase 1-4 clinical trialsDemonstrated experience in management of CROs, in vendor selectionPossessing excellent interpersonal and communication skills, with demonstrated leadership attributesPositioned as a subject matter expert in application of US and Global Regulations and Guidance (SOPs, ICH-GCP, FDA-CFR, ethical standards)Broad scope experience in data collection, monitoring, cleaning and analysis throughout clinical development (Phase 1-4)The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation.Physical Demands and Activities RequiredMust be able to remain in a stationary position standing or sitting for prolonged periods of time.Must be able to move about inside an office and exert up to 10 pounds of force occasionally or a negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects.Must have visual acuity to perform activities such as: preparing and analyzing data and figures, viewing a computer screen, and extensive reading.This position requires repetitive motion, substantial movements (motions) of the wrist, hands, and/or fingers.Must be able to communicate with others to exchange information.Mental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlinesWork EnvironmentThis job operates in a professional or remote office environment and requires operating standard office equipment and keyboards.#LI-remote