2 дня назад
Clinical Research Project Manager - Breast Oncology
76 910 - 85 295$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Clinical Research Project Manager - Breast Oncology (Clinical Trials): Managing multi-center, PI-initiated breast oncology clinical trials across startup, active, and close-out phases with an accent on regulatory compliance, trial documentation, and cross-functional coordination. Focus on maintaining Trial Master Files, developing protocols and consent forms, designing case report forms, and tracking project milestones, safety events, and study databases.
Location: Fully remote from a New England state (ME, VT, NH, MA, CT, or RI) with occasional onsite time in Boston, Massachusetts.
Salary: $76,910–$85,295 per year.
Company
conducts cancer research, provides patient care, and develops treatments through partnerships with Harvard Medical School-affiliated hospitals.
What you will do
- Manage day-to-day operations, budgets, resources, timelines, and milestones for assigned breast oncology clinical trials.
- Coordinate startup, active, and close-out phases of multi-center and PI-initiated trials.
- Develop and maintain Trial Master Files and other essential regulatory documentation in line with GCP standards.
- Assist the Principal Investigator with protocols, consent forms, amendments, reports, and data summaries.
- Design case report forms and maintain study databases with accurate, compliant data.
- Train research staff, coordinate meetings, track safety events, and communicate with stakeholders and regulatory authorities.
Requirements
- Bachelor's degree in a field relevant to clinical research.
- At least three years of experience in clinical research or project management, ideally involving multi-center oncology trials.
- Basic understanding of clinical trial processes, regulatory requirements, and Good Clinical Practice guidelines.
- Familiarity with clinical trial management tools such as EPIC and OnCore.
- Strong organization, communication, documentation, problem-solving, and time-management skills.
- Ability to work remotely only from Maine, Vermont, New Hampshire, Massachusetts, Connecticut, or Rhode Island, with occasional onsite attendance in Boston.
Nice to have
- Experience working in an academic institution.
- Experience coordinating and managing oncology clinical trials.
Culture & Benefits
- Full-time position with a primarily remote work arrangement.
- Work within an innovative, inclusive, and equitable cancer research and patient-care environment.
- Collaborate with faculty, research staff, external partners, and Harvard Medical School-affiliated hospitals.
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