Cardiology Research Coordinator I: Launch Your Impact

Mount Sinai

New York (NY)

Hybrid

USD 59,000 - 74,000

Full time

14 days+
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Job summary

Mount Sinai Health System in the United States is seeking a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study data, and assist in grant preparation and IRB filings.

The role involves maintaining source documents, registering subjects, and handling specimens and monitoring visits as per protocol. Experience is preferred but not required. Based in Kentucky with opportunities across clinical research settings.

Qualifications

  • Bachelor's or Master's degree in Science or closely related field.
  • No experience required. One year of research experience preferred.

Responsibilities

  • Collects and records study data. Inputs all information into database.
  • Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
  • Assists in activities related to clinical research studies including answering calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
  • Assists in preparing grant applications, IRB/ GCO for submission and filings.
  • Maintains source documents and subject files; ensures accurate compilation of subject data via chart reviews.
  • Secures, delivers and ships clinical specimens as required by the protocol.
  • Prepares for monitoring visits.
  • Performs other related duties.

Education

Bachelor's or Master's degree in Science or closely related field

Job description

Mount Sinai Health System in the United States is seeking a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study data, and assist in grant preparation and IRB filings.

The role involves maintaining source documents, registering subjects, and handling specimens and monitoring visits as per protocol. Experience is preferred but not required. Based in Kentucky with opportunities across clinical research settings.

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