CLINICAL PROJECT MANAGER II – IMMUNOLOGY (Sponsor Dedicated/ Remote- US)

Job Responsibilities: CLINICAL PROJECT MANAGER II – IMMUNOLOGY Sponsor Dedicated | Remote – United States. Are you passionate about advancing innovative therapies for patients living with autoimmune and inflammatory diseases? We are seeking experienced Clinical Project Managers with strong global immunology clinical trial experience to join a high-performing sponsor-dedicated team supporting a diverse portfolio of immunology studies across multiple indications and phases of development. This is a fully remote, US-based opportunity, with up to 25% travel, where you will play a critical role in the operational leadership and execution of global clinical trials. We are specifically seeking professionals with 3+ years of hands‑on Clinical Project Management experience leading global immunology studies and collaborating with cross‑functional teams, vendors, and international stakeholders.

WHAT YOU'LL DO: As a Clinical Project Manager II, you will help drive the operational execution and delivery of global immunology clinical trials, ensuring studies are conducted efficiently, compliantly, and according to established timelines. Support and partner with Clinical Study Leads and cross‑functional study teams on global immunology trials Lead day‑to‑day study management activities across study startup, conduct, maintenance, and closeout Manage study timelines, deliverables, risks, and issue resolution Oversee external vendors, CROs, central laboratories, specialty providers, and other study partners Coordinate Clinical Team meetings and drive action item follow‑up Support study‑level planning, forecasting, and operational strategy execution Monitor study performance metrics and proactively identify areas requiring intervention Ensure inspection readiness and compliance with applicable regulations and sponsor requirements Collaborate with stakeholders across Clinical Operations, Data Management, Biostatistics, Medical Monitoring, Regulatory Affairs, Safety, Supply Chain, and Quality Contribute to study status reporting and executive‑level communications Support achievement of study milestones, enrollment targets, database locks, and study closeout activities Travel up to 25% WHAT YOU WILL BRINGRequired Qualifications Bachelor's degree in a scientific, healthcare, or related field 3+ years of Clinical Project Management experience supporting global immunology clinical trials Experience managing studies across multiple countries and regions (North America, Europe, Asia‑Pacific, Latin America, or other global regions) Vendor management experience required Strong understanding of clinical trial operations and study lifecycle management Experience supporting Phase I, Phase II, Phase III, and/or Phase IV immunology studies Strong working knowledge of ICH‑GCP guidelines and clinical research regulations Proficiency with Microsoft Office Suite Ability to work effectively within global, cross‑functional matrix organizations IMMUNOLOGY THERAPEUTIC AREA EXPERIENCECandidates should have direct clinical trial experience supporting one or more immunology indications, including but not limited to: Gastroenterology / Inflammatory Bowel Disease (IBD) Ulcerative Colitis (UC) Crohn's Disease (CD) Autoimmune and Inflammatory Diseases Rheumatoid Arthritis (RA) Psoriatic Arthritis (PsA) Ankylosing Spondylitis (AS) Axial Spondyloarthritis (axSpA) Systemic Lupus Erythematosus (SLE) Sjögren's Syndrome Vasculitis Other Autoimmune Disorders Dermatology Plaque Psoriasis Atopic Dermatitis (Eczema) Hidradenitis Suppurativa Vitiligo Other Immune‑Medicated Dermatologic Diseases Respiratory and Allergy Severe Asthma Eosinophilic Disorders Chronic Rhinosinus