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Stony Brook University · 13 hours ago

Cancer Clinical Trials Study Coordinator

Stony Brook, NY

Full-time

Onsite

Mid Level

$65K/yr - $80K/yr

3+ years exp

Stony Brook University is seeking a Cancer Clinical Trials Study Coordinator who will provide administrative support and interface with management throughout the hospital. The role involves recruiting and enrolling research subjects, coordinating multiple Oncology Cancer Clinical Trials, and educating patients and staff on the research process.

Higher Education

No H1B

Responsibilities

Recruit and enroll research subjects and schedule patients

Attend Tumor Board conferences, participate in hospital rounds and staff meetings and review surgical and pathology reports of cancer patients for protocol candidates

Review present protocol patients on therapy to assure toxicity and response to treatment

Follow and maintain records on protocol patients for the duration of the study

Coordinate multiple Oncology Cancer Clinical Trials from inception to closure under the direction of Principal Investigator/Cancer Clinical Trials Administrative Director

Includes screening, eligibility, data collection, adverse event reporting, completion of CRF's and all regulatory requirements per protocol

Plan and coordinate industry-sponsored, cooperative group and investigator initiated clinical research projects including meeting with industry representatives, contract coordination and budget negotiation

Acts as a resource between outside sponsors, industries and SUNY

Draft informed consent forms, assent forms, and other documentation for submission to the IRB

Patient/Staff Education – Educate patients and families as well as oncology staff on the research process and investigational cancer drugs

Other duties as assigned

Qualification

Clinical research experienceOncology clinical trialsIRB/regulatory knowledgeMicrosoft Office proficiencyMedical terminology knowledgeCommunication skillsOrganizational skills

Required

Bachelor's degree (foreign equivalent or higher). In lieu of a Bachelor's degree, a combination of clinical/healthcare, medical type industry setting and/or human research experience totaling four (4) years may be considered

Three (3) years of full-time experience in a clinical/healthcare or medical type industry setting

One (1) year of human research experience

Knowledge of medical terminology