10 часов назад
Senior Clinical Trial Manager (Oncology)
143 000 - 173 250$
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Описание вакансии
Текст:
TL;DR
Senior Clinical Trial Manager (Oncology) (Clinical Operations): Leading global oncology clinical trials from planning through closeout with an accent on regulatory compliance, patient recruitment, data integrity, and cross-functional execution. Focus on overseeing trial teams and vendors, managing clinical supplies and documentation, and delivering studies within timelines, budgets, and ICH-GCP requirements.
Location: Hybrid, with a minimum of 3 days per week onsite at either the Millbrae, CA or Jersey City, NJ office; additional onsite presence may be required based on business needs.
Salary: $143,000–$173,250 per year, plus bonus and equity compensation.
Company
Therapeutics is a biopharmaceutical company developing novel treatments through a platform combining chemistry, engineering, computation, biology, and molecular-resolution live-cell microscopy.
What you will do
- Develop and execute strategic plans for global clinical trials, including planning, monitoring, execution, and closeout.
- Lead and mentor clinical trial associates, coordinators, and specialists.
- Coordinate clinical and ancillary supplies, import and export requirements, filing, archiving, retention, and insurance processes.
- Ensure studies follow approved protocols, ICH-GCP, EMEA, PMDA, and other applicable regulations and SOPs.
- Oversee patient recruitment, data collection and validation, quality control, documentation, and country information in clinical, regulatory, safety, and finance systems.
- Collaborate with investigators, study coordinators, vendors, and cross-functional stakeholders while managing trial budgets and resources.
Requirements
- Postgraduate degree with 6+ years of relevant experience or bachelor's degree with 8+ years of relevant experience in life sciences, healthcare, or a related field.
- Substantial clinical trial management experience, including leadership responsibilities.
- In-depth knowledge of clinical trial processes, regulations, and industry best practices.
- Strong organizational skills, meticulous attention to detail, and exceptional communication and leadership capabilities.
- Proficiency with Microsoft Office Suite and clinical trial management software.
- Ability to work onsite at least 3 days per week in Millbrae, California, or Jersey City, New Jersey.
Culture & Benefits
- Collaborative, fast-paced, and evolving work environment focused on advancing patient care.
- 401(k) plan with company matching.
- Medical, dental, vision, mental health, and wellness benefits.
- Generous paid time off, holiday policies, and weeklong summer and winter holiday shutdowns.
- Enhanced parental leave and life/AD&D insurance benefits.
- Daily subsidized lunch when working onsite.
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