Remote Clinical Trial Coordinator | Docs & Compliance Lead

Parexel

United States

Remote

USD 65.000 - 90.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Parexel FSP is seeking a Clinical Trial Coordinator to support trial administration, document management, and regulatory tasks from anywhere in the United States. You will work with site staff and internal teams to ensure timely data collection, filing, and study tracking in CTMS.

The role requires 1–2 years in clinical research, proficiency with MS Office, strong communication, and the ability to work independently in a matrix, multicultural environment, while following GCP and Parexel SOPs.

Qualifikationen

  • 1–2 years in Clinical Research or healthcare experience.
  • Understanding of Global/Country/Regional Clinical Research Guidelines.
  • Knowledge of Good Documentation Practices.
  • Strong IT skills and MS Excel proficiency.
  • ICH-GCP knowledge appropriate to role.
  • Strong communication and time-management abilities.
  • Ability to work independently in a matrix multicultural environment.
  • Customer-focused attitude.

Aufgaben

  • Track essential documents and report safety reports.
  • Maintain study tools, documents and CTMS trackers.
  • Coordinate labeling and translation change requests.
  • Prepare Investigator trial file binders and execute eTMF QC.
  • Support IRB/ERC submissions and regulatory filings.
  • Organize investigator meetings and related materials.
  • Adhere to Parexel SOPs and processes.

Kenntnisse

Clinical Research
GCP knowledge
MS Excel
IT skills
Communication skills
Time management
Multicultural teamwork

Ausbildung

B.A./B.S. in Life Sciences

Tools

CTMS
eTMF
MS Office

Jobbeschreibung

Parexel FSP is seeking a Clinical Trial Coordinator to support trial administration, document management, and regulatory tasks from anywhere in the United States. You will work with site staff and internal teams to ensure timely data collection, filing, and study tracking in CTMS.

The role requires 1–2 years in clinical research, proficiency with MS Office, strong communication, and the ability to work independently in a matrix, multicultural environment, while following GCP and Parexel SOPs.

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