Clinical Data Manager II [Contract]

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. Overview The Clinical Data Manager II will be responsible for assisting the lead data manager in end-to-end Data Management activities. He/she will participate as an active member of a multi-disciplinary team to plan, lead and execute the Data Management tasks required for phase 1-4 studies. The candidate must have a broad, fundamental knowledge of the data management process and should be able to perform most required tasks with guidance after receiving instructions and / or training The Clinical Data Manager II should be able to: Essential Functions and Responsibilities Ensure the integrity, accuracy and compliance of clinical trial data Assist during a study database in RAVE to include but not limited to: Review protocols for appropriate data capture including electronic Case Report Form (eCRF) design Assist with the development of data edit check specifications and data listings Perform User Acceptance Testing (UATs) of Electronic Data Capture (EDC) systems according to company processes Assist with the review of migration reports to ensure database build accuracy Perform reconciliation of data from external data sources against the clinical database Perform Serious Adverse Event reconciliation activities according to SOPs and guidelines Execute data cleaning and discrepancy management to ensure compliance with the protocol Track and report study metrics to internal and external stakeholders Create or update Data Management Plan (DMP), Data Review Plan (DRP), eCRF Completion Guidelines (eCCGs) and other Data Management required study documents Perform database lock and freeze activities per company SOPs Required Education, Skills, and Knowledge At a minimum, Bachelor's degree required in the scientific or healthcare field At least 5 years' experience in Data Management for the pharmaceutical / biotechnology industry, or equivalent experience in an FDA-regulated environment including study lead experience Oncology experience is a must RAVE database experience is preferable Must have good time management skills and a proven ability to multitask Possesses a comprehensive understanding of regulatory guidelines and industry standards (e.g., ICH/FDA guidance, CDISC standards, GCDMP, 21 CFR 11, MedDRA, WHO Drug Dictionaries, etc.) and their application to Data Management practice. Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors. Possesses strong English language written and verbal communication skills. Able to travel to off-site meetings or training seminars as needed. Possesses solid computer system and technical skills with a strong ability to learn multiple computer applications. Experience in Coding (MedDRA and WHODrug), Site and User Management and Lab Normal Range (LNR) entry in Rave is a plus Must be able to work collaboratively in a fast-paced environment 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 Required Must be able to remain in a stationary position standing or sitting for prolonged periods of Must be able to move about inside an ... (truncated, view full listing at source)