Clinical Research Coordinator — Patient-Centric Trials

Mount Sinai Medical Center of Florida, Inc.

Miami Beach, Northern (FL, KY)

Ibrido

USD 55.000 - 75.000

Tempo pieno

3 giorni fa
Candidati tra i primi
Generatore di candidature

Trasforma questa posizione in un colloquio — un curriculum e una lettera di presentazione creati in base a ciò questo datore di lavoro sta cercando.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Health benefits
Life insurance
Long-term disability coverage
Retirement plan
Paid time off
Tuition reimbursement
Wellness program
Employee assistance program
On-site housing for select positions
Pet Insurance

Descrizione del lavoro

Mount Sinai Medical Center of Florida, Inc. in Miami Beach seeks a Clinical Research Coordinator to screen participants, document progress, and support protocol adherence across trials.

You will interact with patients and families, coordinate data entry, and assist with regulatory documentation, monitoring study visits, and communicating findings to the study team. The role requires a Bachelor's degree (preferred) and at least one year in medical or research settings; certification is a plus.

Competenze

  • Bachelor's degree preferred in a research-related field.
  • Minimum 1 year of medical/research background preferred.
  • Related Field Certification preferred.

Mansioni

  • Screen participant patients and document progress per protocol.
  • Inform physicians of patient responses and protocol adherence.
  • Coordinate data entry and regulatory documentation for studies.
  • Monitor patients during treatments and ensure required tests are performed.
  • Communicate with monitors/auditors and study staff to ensure compliance.

Conoscenze

Communication
Empathy
Attention to detail
Data entry

Formazione

Bachelor's degree preferred

Descrizione del lavoro

Mount Sinai Medical Center of Florida, Inc. in Miami Beach seeks a Clinical Research Coordinator to screen participants, document progress, and support protocol adherence across trials.

You will interact with patients and families, coordinate data entry, and assist with regulatory documentation, monitoring study visits, and communicating findings to the study team. The role requires a Bachelor's degree (preferred) and at least one year in medical or research settings; certification is a plus.

Ottieni la revisione del curriculum gratis e riservata.

o trascina qui il file.

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