2 дня назад
Clinical Research Project Manager I
76 910 - 85 295$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Research Project Manager I (Clinical Trials/Oncology): Managing multi-center, PI-initiated 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, managing case report forms and databases, and tracking milestones, safety events, and project variances.
Location: Boston, Massachusetts, United States; hybrid with 2–3 days onsite per week
Salary: $76,910–$85,295 per year
Company
conducts cancer research and provides comprehensive patient care while advancing treatments and educating physician-researchers.
What you will do
- Manage the daily operations, budgets, resources, timelines, and milestones of assigned clinical trials.
- Coordinate startup, active, and close-out phases for primarily PI-initiated and multi-center studies.
- Develop and maintain Trial Master Files in accordance with Good Clinical Practice standards and institutional policies.
- Assist Principal Investigators with protocols, consent forms, amendments, case report forms, reports, and data summaries.
- Maintain study databases and support data integrity, regulatory submissions, safety-event tracking, and communication with regulatory authorities.
- Coordinate research meetings, conference calls, mailings, training, and collaboration with internal and external stakeholders.
Requirements
- Bachelor's degree relevant to clinical research.
- 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 organizational, time-management, documentation, communication, and problem-solving skills.
- Ability to work onsite in Boston 2–3 days per week and collaborate effectively with research staff, regulatory authorities, cross-functional teams, and external partners.
Nice to have
- Experience working in an academic institution.
- Experience coordinating and managing clinical research operations.
Culture & Benefits
- Inclusive, diverse, and equitable environment focused on compassionate patient care.
- Work supporting cancer research, treatment advances, and public health programs.
- Collaboration with Harvard Medical School-affiliated hospitals and external research partners.
- Commitment to ethical clinical research and patient confidentiality.
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