1 день назад
Senior Clinical Trial Associate (Oncology)
110 000 - 115 000$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Senior Clinical Trial Associate (Oncology): Supporting the execution of in-house and outsourced oncology clinical trials with an accent on study documentation, vendor coordination, investigator-site communication, and Trial Master File quality. Focus on overseeing sample logistics, reconciling study processes, managing operational risks, and coordinating contracts, budgets, invoices, and payments.
Location: Based out of the San Francisco or Cambridge office; approximately 10% travel required
Salary: $110,000–$115,000 annually, plus equity, bonus, and benefits.
Company
is a clinical-stage biopharmaceutical company developing therapies for breast cancer, including palazestrant and OP-3136.
What you will do
- Provide administrative and operational support to Clinical Trial Leads and Study Execution Teams across study start-up, maintenance, and closeout.
- Coordinate clinical trial activities with internal teams, investigator sites, CROs, contract laboratories, and other vendors.
- Manage study documentation, correspondence, materials, trackers, financial records, and Trial Master File activities.
- Oversee sample collection, shipment, and analysis, while reconciling study processes and escalating issues.
- Support vendor management plans, study metrics, contracts, budgets, invoices, payments, central IRB submissions, and site-specific informed consent forms.
- Contribute to Clinical Operations initiatives, SOPs, quality control reviews, meeting coordination, and departmental administration.
Requirements
- Bachelor’s degree.
- At least 3 years of related industry experience, including 2 years working as a Clinical Trial Associate.
- Working knowledge of clinical protocols and proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.
- Experience leading small-group meetings and/or managing vendor relationships.
- Strong organization, attention to detail, teamwork, collaboration, and written and verbal communication skills.
- Ability to accommodate a flexible work schedule according to clinical trial priorities.
Nice to have
- Familiarity with FDA and EMA regulatory requirements and ICH/GCP guidelines.
Culture & Benefits
- Competitive compensation and benefits package.
- Equity and bonus opportunities.
- Open, flexible, and friendly work environment.
- Support for long-term career development.
- Culture focused on excellence, adaptability, collaboration, and improving patient outcomes.
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