Miami Beach, Florida, US
11 hours ago
Clinical Research Coordinator

Research Coordinator - Oncology - On site on Miami Beach

One year grant funded position -  Utilizing navigation and education to improve NCCN guideline-driven care quality for patients with gastric and gastroesophageal junction (GEJ) malignancy in regions of Florida

As Mount Sinai grows, so does our legacy in high-quality health care.

Since 1949, Mount Sinai Medical Center has remained committed to providing access to its diverse community. In delivering an unmatched level of clinical expertise, our medical center is committed to recruiting and training top healthcare workers from across the country. We offer the latest in advanced medicine, technology, and comfort in 12 facilities across Miami-Dade (including our 674-bed main campus facility) and Monroe Counties, with 38 medical services, including cancer care, 24/7 emergency care, orthopedics, cardiovascular care, and more. Mount Sinai takes pride in being South Florida's largest private independent not-for-profit hospital,dedicated to continuing the training of the next generation of medical pioneers.

Culture of Caring: The Sinai Way

Our hardworking, tight-knit community of more than 4,000 dedicated employees fosters an environment of care and compassion. Each member plays a vital role in our collective mission to deliver excellent healthcare through innovation, education, and research. At Mount Sinai, we take pride in our achievements, aiming to be a beacon of quality healthcare in South Florida. We welcome all healthcare professionals to join our thriving community and contribute to our pursuit for clinical excellence.

Position Responsibilities

Performs screening of potential research subjects, verifying eligibility criteriaEnsures documentation of patient’s progress throughout the research processConducts patient research visits in coordination with physiciansAdheres to protocol schedule and facilitates inter-departmental scheduling for procedures/testsExtracts data from patient charts to record and submit information to study sponsors, both electronically and written submissionsEnsures compliance with protocol guidelinesWorking knowledge and adherence to the Code of Federal Regulations and Good Clinical PracticesReports Adverse Events to appropriate agencies and Institutional Review BoardWorks with monitors and sponsors to assure accuracy of subject charts and data collectionResolves data queriesAssists with preparation for National Cancer Institute and FDA auditsParticipates in internal audits and quality compliance as outlined in the Code of Federal Regulation and Good Clinical PracticesCoordinates the collection and shipment of ancillary specimensPrepare study progress reports as needed

Requirements

Related Field Certification / Research Professional preferredBachelors Degree in the respective research related field.Minimum 2 years of medical / research background.Excellent written and oral communication skillsComputer skills required, proficient with all Microsoft applications

Benefits 

We believe in the physical and mental well-being of our employees and are committed to offering comprehensive benefits that fit their personal needs. Our robust employee benefits package includes:

Health benefitsLife insuranceLong-term disability coverageHealthcare spending accountsRetirement planPaid time offPet InsuranceTuition reimbursementWellness program

 

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