Senior Clinical Trials Manager

🕒 il y a 19 jours

🏄 California – Distant

🏄 California – Remote

💵 $143 000 - $165 000 / an

⏰ Temps Plein

🟠 Senior

👔 Manager

👻 Score fantôme 0%

Ce que ça veut dire : la probabilité que cette offre reste ouverte sans recrutement actif.Comment le lire : 60 % ou plus, on pense que c'est une offre fantôme. Un score plus bas est moins inquiétant.Comment on la calcule : ancienneté, republications, postes ouverts vs taille de l'équipe, rapidité de clôture, et si le salaire est indiqué.À noter : une estimation à partir de données publiques, pas un jugement sur l'entreprise. De vraies offres peuvent avoir un score élevé, alors prenez-le comme un indice, pas comme un fait.

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ImmunityBio, Inc.

Site WebLinkedInTous les Emplois

501 - 1000 employés

🏥 Santé

💼 Conseil

🏭 Fabrication

Healthcare • Consulting • Manufacturing

ImmunityBio, Inc. est une entreprise de biotechnologie axée sur le développement d'immunothérapies innovantes pour renforcer la capacité du système immunitaire à combattre le cancer et les maladies infectieuses. En exploitant la puissance de la réponse immunitaire de l'organisme, ImmunityBio vise à fournir des traitements révolutionnaires qui peuvent améliorer les résultats et la longévité des patients atteints de maladies difficiles.

Description

• Manage activities of several global clinical studies • Assist the Clinical Project Manager in developing and managing company-sponsored global clinical trials • Review completed assignments by members of the clinical development group • Develop and manage revisions to informed consents, laboratory manuals, pharmacy manuals, CRFs, and other study execution tools • Support site recruitment, site initiation, site payments, and site close-out • Oversee training of new clinical site staff and training for protocol amendments • Liaise with the in-house team to collect updated regulatory documents • Provide daily guidance to clinical sites on protocol interpretation and safety compliance • Train clinical development group staff • Prepare and update clinical trial updates for the Clinical Development team • Summarize and maintain patient treatment, response, and survival data for active studies • Create, edit, and adhere to SOPs, process improvements, and standardized templates • Perform ad-hoc and cross-functional duties and projects as assigned

🎯 Exigences

• Bachelor’s degree with 7+ years of relevant experience in clinical research required • Proficiency in MS Word, Excel, PowerPoint, Outlook • Excellent written/oral communication skills • Strong organizational and multi-tasking skills • Understand and adhere to job-specific systems, processes, and company SOP requirements • Maintain corporate confidentiality at all times • Ability to work in a standard office setting and use standard office equipment, including a computer • Ability to lift and carry materials weighing up to 20 pounds • Ability to travel approximately 20% of the time

🏖️ Avantages

• Opportunity to join a publicly traded biopharmaceutical company • Collaborative team with ability to work across different areas of the company • Professional development opportunities • Discretionary bonus • Equity award • Medical, Dental and Vision Plan Options • Health and Financial Wellness Programs • Employer Assistance Program (EAP) • Company Paid and Voluntary Life/AD&D • Short-Term and Long-Term Disability • Healthcare and Dependent Care Flexible Spending Accounts • 401(k) Retirement Plan with Company Match • 529 Education Savings Program • Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks • Paid Time Off (PTO), including 11 Holidays • Unlimited PTO for Exempt Employees • 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day for Non-Exempt Employees • Tools and resources to optimize Health and Wellness