Senior Clinical Operations Manager – Trials & Teams

Premier Research

New York (NY)

Vor Ort

USD 99.000 - 121.000

Vollzeit

Vor 10 Tagen

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Premier Research is seeking a Manager, Clinical Operations to join our Clinical Monitoring, Site Management and SSU team in New York. You will lead clinical operations resources and mentor staff across Phase I–IV trials while ensuring client deliverables and regulatory compliance.

The role requires 6+ years in clinical research and at least 3 years in a supervisory capacity, with travel as needed. We value collaboration and a commitment to quality in a dynamic, matrix environment.

Qualifikationen

  • Recognized undergraduate degree is required.
  • A degree in Pharmacy, Biology, Chemistry, Psychology, Nursing or a related discipline is preferred.

Aufgaben

  • Manages clinical operations employee resources and projections to meet client expectations and obligations.
  • Interfaces with other departments to design cross-functional process efficiencies or develop new approaches to clinical management and monitoring of trials (Phase I-IV).
  • Ensures audit preparedness of Clinical Operations employees, including training records, processes, and SOP compliance.
  • Directs development and management of departmental performance metrics, training and standards for assigned regions.
  • Moves projects forward by sourcing staff and utilizing available tools.
  • Mentors, coaches and trains all employees.

Kenntnisse

People management
Leadership
Cross-functional collaboration
Mentoring
Interpersonal skills

Ausbildung

Undergraduate degree
Preferred fields: Pharmacy, Biology, Chemistry, Psychology, Nursing

Jobbeschreibung

Premier Research is seeking a Manager, Clinical Operations to join our Clinical Monitoring, Site Management and SSU team in New York. You will lead clinical operations resources and mentor staff across Phase I–IV trials while ensuring client deliverables and regulatory compliance.

The role requires 6+ years in clinical research and at least 3 years in a supervisory capacity, with travel as needed. We value collaboration and a commitment to quality in a dynamic, matrix environment.

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