Description

<div class="content-intro">Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&amp;D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. &nbsp; Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson &amp; Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. &nbsp;</div>Legend Biotech is seeking an Early Stage Drug Development Project Manager as part of the Early-Stage Drug Development team based in Somerset, NJ. Role Overview We are seeking a seasoned Project Manager to support preclinical and early clinical development at Legend. The successful candidate will oversee and coordinate cross-functional efforts related to preclinical research and the advancement of cell therapy products through early clinical stages. This position is responsible for ensuring that all programs progress according to timelines, remain within scope, and comply with regulatory, quality, and scientific standards. The Project Manager will collaborate extensively with Research, Translational Science, CMC, Regulatory Affairs, Clinical Operations, Quality, and external stakeholders to facilitate execution from late-stage discovery through IND-enabling studies and early-phase clinical trials. Legend remains dedicated to developing innovative cell therapy solutions aimed at addressing unmet medical needs. As a member of the Preclinical and Early Clinical Development team, the Project Manager will be integral to fostering effective collaboration and driving efficient advancement of research initiatives. Key Responsibilities Program &amp; Project Management <ul> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Working closely with project lead, develop and maintain integrated project plans for Project team covering preclinical, CMC, regulatory, and early clinical activities.</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Drive execution of program timelines, milestones, budgets, and resource plans.</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Track deliverables, identify risks, and implement mitigation strategies.</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Facilitate governance meetings, project team meetings, and decision-making forums.</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Prepare clear project status updates, dashboards, and executive-level reports.</li> </ul> Preclinical &amp; Translational Development <ul> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Coordinate in vitro and in vivo studies, including pharmacology, toxicology, biodistribution, and tumorigenicity (as applicable).</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Manage interactions with CROs and academic collaborators conducting preclinical studies.</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Ensure studies are conducted in alignment with regulatory expectations for IND submissions.</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Support data integration and readiness for regulatory filings and internal reviews.</li> </ul> Early Clinical Development Support <ul> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Support planning and execution of first-in-human and early-phase (Phase 1/1b) clinical studies.</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Coordinate cross-functional inputs for clinical trial readiness (clinical operations, CMC, QA, regulatory).</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Assist with clinical timelines, site activation planning, and investigational product readiness.</li> </ul> Regulatory &amp; Quality Interface <ul> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Support preparation of IND-enabling documentation and regulatory submissions.</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Track regulatory commitments within EDD.</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Ensure project activities align with GxP and internal quality systems.</li> </ul> Vendor &amp; Stakeholder Management <ul> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Manage external vendors, CROs, and consultants, including scope, timelines, and deliverables.</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Foster effective collaboration across internal teams and external partners.</li> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Serve as a central point of communication for program execution.</li> </ul> Decision Making <ul> <li style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Have the ability to drive project timeline</li> </ul> Requirements <ul> <li class="col-xs-12 no-horiz-padding" style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Bachelor’s degree in life sciences, bioengineering, or related field required.</li> <li class="col-xs-12 no-horiz-padding" style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Advanced degree (MS, PhD) preferred.</li> <li class="col-xs-12 no-horiz-padding" style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">3–7+ years of project management experience in biotechnology or pharmaceutical development.</li> <li class="col-xs-12 no-horiz-padding" style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Hands-on experience supporting preclinical and/or early clinical development programs.</li> <li class="col-xs-12 no-horiz-padding" style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Experience in cell therapy, gene therapy, or other advanced therapies strongly preferred.</li> <li class="col-xs-12 no-horiz-padding" style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Familiarity with IND-enabling studies and early-phase clinical development.</li> <li class="col-xs-12 no-horiz-padding" style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Strong understanding of drug development processes, especially for cell-based therapies.</li> <li class="col-xs-12 no-horiz-padding" style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Proven ability to manage complex, cross-functional programs in a fast-paced environment.</li> <li class="col-xs-12 no-horiz-padding" style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Excellent organizational, communication, and stakeholder-management skills.</li> <li class="col-xs-12 no-horiz-padding" style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Experience with project management tools (e.g., MS Project, Smartsheet, Planisware).</li> <li class="col-xs-12 no-horiz-padding" style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Ability to identify risks early and drive pragmatic solutions.</li> </ul> #Li-JR1 #Li-Hybrid<div class="content-pay-transparency"><div class="pay-input"><div class="description">The base pay range below is what Legend Biotech USA Inc. reasonably expects to offer at the time of posting. Actual compensation may vary based on experience, skills, qualifications, and geographic location. The company reserves the right to modify this range as needed and in accordance with applicable laws. Other Types of Pay: Performance-based bonus and/or equity is available to employees in eligible roles. Benefits and Paid Time Off: Medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer eight (8) weeks of paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays. Additional voluntary benefits include flexible spending and health savings accounts, life and AD&amp;D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.</div><div class="title">Pay Range (Base Pay): </div><div class="pay-range">$93,463&mdash;$122,670 USD</div></div></div><div class="content-conclusion">Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech. &nbsp; EEO Statement It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances. &nbsp; Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. <div>&nbsp;</div> <div>For information related to our privacy policy, please review:&nbsp;<a href="https://legendbiotech.com/privacy-policy-2/" target="_blank">Legend Biotech Privacy Policy.</a></div></div>