14 дней назад
Clinical Trial Manager II, IQVIA Biotech (Oncology)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Trial Manager II, IQVIA Biotech (Oncology): Delivering global oncology clinical trials in compliance with regulatory, protocol, customer, and internal requirements with an accent on recruitment, clinical quality, risk mitigation, project finances, and stakeholder management. Focus on leading cross-geography clinical teams, building operational plans, managing delivery risks and financial changes, and supporting milestone achievement across the trial lifecycle.
Location: Mexico City, Mexico
Employment type: Full time
Company
Biotech partners with biotech and emerging biopharma companies to support clinical development across phases and therapeutic areas. provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Lead clinical delivery for assigned oncology studies in line with ICH-GCP, protocols, contracts, policies, SOPs, and project plans.
- Manage recruitment targets and strategies, clinical risks, quality standards, compliance monitoring, and issue resolution.
- Oversee clinical project finances, including estimates at completion, baseline changes, scope, and additional service opportunities.
- Lead internal and external stakeholder communication and collaborate with Project Leaders and functional teams to achieve milestones.
- Plan resources, guide clinical teams, conduct meetings and training, and provide feedback supporting professional development.
- Contribute to clinical delivery strategies, bid defenses, proposals, and clinical operations plans; attend site visits when applicable.
Requirements
- Bachelor's degree in healthcare or another scientific discipline.
- At least 5 years of clinical research or monitoring experience, or an equivalent combination of education, training, and experience.
- Knowledge of project management practices, clinical trial conduct, applicable local laws, and ICH-GCP regulatory requirements.
- Broad protocol and therapeutic knowledge, understanding of the clinical research industry, and knowledge of project finances.
- Good command of English, with strong written and verbal communication skills.
- Problem-solving, organization, prioritization, attention to detail, leadership, negotiation, mentoring, collaboration, and Microsoft Office skills.
Culture & Benefits
- Collaborative work with clinical teams, Project Leaders, clients, and cross-functional stakeholders.
- Exposure to global clinical trials and collaboration across geographies and cultures.
- Opportunities to mentor peers and support professional development.
- Work focused on accelerating innovative medical treatments and improving patient outcomes.
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