Clinical Research Coordinator: Launch Your Research Career

Mount Sinai Morningside

New York (NY)

Vor Ort

USD 60.000 - 90.000

Vollzeit

Vor 8 Tagen

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily study activities, obtain informed consent, collect and organize data, and assist with grant applications and IRB/Grants submissions. This role involves data entry, chart reviews, and coordinating with study teams.

Responsibilities include maintaining study documents and specimens, preparing for monitoring visits, screening participants, and ensuring regulatory filings are complete.

Qualifikationen

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

Aufgaben

  • Collects and records study data and inputs information into a database.
  • Obtains informed consent under minimal supervision and educates participants regarding study requirements.
  • Assists in activities related to clinical research including screening participants, registering subjects, and collecting data.
  • Assists in preparing grant applications, IRB/GCO submissions, and related filings.
  • Maintains source documents and subject files; ensures complete data through chart reviews.
  • Secures, delivers and ships clinical specimens as required by the protocol.
  • Prepares for monitoring visits.
  • Performs other related duties.

Ausbildung

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

Jobbeschreibung

Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily study activities, obtain informed consent, collect and organize data, and assist with grant applications and IRB/Grants submissions. This role involves data entry, chart reviews, and coordinating with study teams.

Responsibilities include maintaining study documents and specimens, preparing for monitoring visits, screening participants, and ensuring regulatory filings are complete.

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