CRA/CRC I: Grow in Protocols, Data & Patients

Massachusetts General Hospital

Boston (MA)

Vor Ort

USD 28.000 - 40.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Mass General Brigham is seeking a Clinical Research Associate/Clinical Research Coordinator I to enroll eligible patients in cancer studies and manage data collection for multiple protocols. The role liaises with the clinical team, sponsor, and IRB to ensure reporting and compliance.

Training covers institutional and federal regulations for clinical research. The position combines data abstraction, regulatory duties, and patient coordination with direct patient contact, under supervision of the

Qualifikationen

  • Excellent attention to detail and accuracy in data collection and entry.
  • Strong organizational and time-management skills for multiple studies.
  • Ability to follow study protocols and sponsor/IRB requirements.
  • Good communication with clinical teams, sponsors, and IRB.
  • Familiarity with electronic medical records and regulatory documents.

Aufgaben

  • Screen potential study participants for eligibility and enrollment.
  • Coordinate tests, procedures, and appointments with care teams.
  • Collect, verify, and manage study data and regulatory documents.
  • Monitor adverse events and report deviations per sponsor and IRB.
  • Prepare regulatory binders and assist with monitoring visits.

Kenntnisse

Attention to detail
Organizational skills
Follow directions
Communication skills
Computer literacy
Clinical research knowledge

Ausbildung

Bachelor's Degree Related Field

Jobbeschreibung

Mass General Brigham is seeking a Clinical Research Associate/Clinical Research Coordinator I to enroll eligible patients in cancer studies and manage data collection for multiple protocols. The role liaises with the clinical team, sponsor, and IRB to ensure reporting and compliance.

Training covers institutional and federal regulations for clinical research. The position combines data abstraction, regulatory duties, and patient coordination with direct patient contact, under supervision of the

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