Clinical Research Coordinator I (Multiple Myeloma) - Hematology & Medical Oncology
Clinical Research Coordinator I (Multiple Myeloma) - Hematology & Medical Oncology
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1 Vacancy
Job Description
A Clinical Research Coordinator (CRC) I position is currently available to support our Multiple Myeloma division within the Tisch Cancer Institute. Duties will include activities such as but no limited to data collection obtaining informed consent and maintaining and organizing study information.
We are looking for highly motivated confident and personable individuals who have excellent communication and organizational skills. The ideal candidate should be comfortable and capable of working with a large multicultural and ethnic demographic of people. Because of the nature of the work we require an individual who has an open and good-natured disposition who could also show empathy understanding and patience.
The Tisch Cancer Institute is a vital component of the Icahn School of Medicine at Mount Sinai Hospital and plays a key role in the Mount Sinai Health System which is one of the largest health care systems in the nation. We are a National Cancer Institute (NCI)-designated center and provide a multidisciplinary approach to cancer treatments and clinical breakthroughs that may one day put an end to cancer.
Responsibilities
- Collects and records study data; inputs all information into database.
- Under direct supervision of the Principle Investigator(s) obtains informed consent and educates participants regarding study requirements.
- Assists in the activities related to clinical research studies including but not limited to: answering phone calls screening participants for eligibility registering subjects with sponsoring agency and administering lifestyle questionnaires.
- Maintains source documents and subject files in accordance with hospital procedures; helps to ensure accurate and complete compilation of subject data through chart reviews.
- Secures delivers and ships clinical specimens as required by the protocol.
- Responsible for organizing and preparing for monitoring visits.
- Assists with coordination and management of clinical trials including communication with Sponsors.
- Performs other related duties as assigned.
Qualifications
- Bachelors or Masters degree in Science or closely related field.
- 1-2 years of research experience
Required Experience:
IC
Employment Type
Full-Time
