3 дня назад
Assistant Clinical Research Manager - Center of Early Detection & Intervention Blood Cancers Interventional Clinical Trials (Clinical Research)
70 000 - 85 300$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Assistant Clinical Research Manager (Clinical Trials): Supporting the management and oversight of interventional cancer clinical trials, including study start-up, active operations, closeout, regulatory compliance, data management, and staff supervision with an accent on Good Clinical Practice and audit-ready trial execution. Focus on tracking protocol milestones, maintaining essential documents, monitoring enrollment and data compliance, and coordinating corrective actions across clinical research stakeholders.
Location: Hybrid in Boston, Massachusetts, with 2–3 onsite days per week; remote workdays are limited to Maine, Vermont, New Hampshire, Massachusetts, Connecticut, or Rhode Island.
Salary: $70,000–$85,300 per year
Company
conducts cancer research, clinical trials, patient care, and medical education in partnership with Harvard Medical School-affiliated hospitals.
What you will do
- Support oversight of the Blood Cancers interventional clinical trial portfolio and related regulatory and compliance activities.
- Coordinate study start-up, active trial operations, and closeout activities, including protocol development and milestone tracking.
- Support patient enrollment, protocol treatment, follow-up care, registration, and interaction with study registrars and pharmaceutical sponsors.
- Maintain essential regulatory documents and clinical trial reporting, including safety events, annual approvals, and deviations.
- Monitor data collection, compliance status, progress reports, and corrective actions with investigators, sponsors, and clinical trial operations stakeholders.
- Support recruitment, onboarding, training, competency assessments, and day-to-day supervision of clinical research staff.
Requirements
- Bachelor’s degree required.
- 3+ years of related experience preferred.
- Understanding of clinical research, cancer treatment modalities, clinical trial start-up, active, and closeout phases.
- Knowledge of local policy and federal and state research regulations, with the ability to identify issues requiring regulatory consultation.
- Experience with protocol development, data compilation and analysis, tracking systems, and Microsoft Office.
- Ability to work independently, think critically, exercise professional judgment, and communicate effectively.
Culture & Benefits
- Inclusive, diverse, and equitable environment focused on compassionate patient care.
- Work on research advancing cancer treatment and public health.
- Patient contact may include individuals of all ages and populations.
- Hybrid work arrangement with regular onsite collaboration in Boston.
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