Hybrid Oncology Clinical Research Coordinator

Actalent

Newark (NJ)

Ibrido

USD 48.000 - 52.000

Tempo pieno

10 giorni fa

Generatore di candidature

Aumenta le possibilità di ricevere una risposta da questo datore di lavoro — un curriculum e una lettera di presentazione personalizzati, che corrispondono esattamente a ciò che sta cercando.

Supera i filtri ATS

Descrizione del lavoro

Actalent in Newark, NJ is seeking a dedicated Clinical Research Coordinator to manage the initiation and activation of oncology trial protocols, coordinate study activities, ensure regulatory compliance, and maintain meticulous research records across multiple sites.

Responsibilities include verifying IRB/HRSC approvals, preparing study tools, developing documents in Excel/Word/Access, obtaining informed consent, and collaborating with the RNC and physicians to monitor adverse events and report

Competenze

2–4 years of clinical research coordinator experience.
Experience in oncology clinical research.
Proficiency in recruitment, screening, enrolling and consenting patients.
Lab processing and handling experience.
Proficiency with Excel, Word and Access.

Mansioni

Verify SRB/IRB/HROC approvals before study activation.
Coordinate preparation of study tools and binders.
Develop study tools using Excel and Word; confirm eligibility via charts/history.
Ensure informed consent is obtained and registered with sponsors.
Maintain comprehensive research records across trial sites.
Collaborate with RNC and physicians to grade adverse events and SAEs.
Provide regular study progress reports to tumor study group and PI.
Liaise with sponsors; schedule monitoring visits and calls.
Ensure compliance with treatment plans and GCP.