Assistant Director for Clinical Trials Operations - 231779
: Job Details :


Assistant Director for Clinical Trials Operations - 231779

Medix™

Location: New Haven,CT, USA

Date: 2024-11-21T15:24:31Z

Job Description:

*RELOCATION PACKAGE OFFERED*

Overview

We are seeking an experienced Clinical Research Operations Manager to oversee and manage clinical trial operations for an oncology-focused clinical trials office. This role requires strong leadership and strategic oversight to ensure operational efficiency, compliance, and quality in clinical trial management. The ideal candidate will have extensive experience in clinical research operations, specifically within oncology, and will work closely with leadership to drive operational improvements and achieve program goals.

Responsibilities

  • Direct and manage clinical trial operations for an oncology-focused clinical trials office, setting strategic goals and developing budgets, policies, and procedures to support operational infrastructure.
  • Provide strategic input on short- and long-term planning for the clinical trials office and develop objectives related to productivity, compliance, communication, and patient satisfaction.
  • Design and implement process improvement initiatives to enhance operational efficiency and meet program goals.
  • Oversee recruiting, hiring, career development, and day-to-day supervision of clinical research professionals, including clinical research managers, project managers, data coordinators, research coordinators, and clinical research nurses.
  • Establish priorities and timelines to ensure efficient and effective trial operations.
  • Collaborate with faculty leaders and deploy resources across teams to support oncology research efforts.
  • Partner with the Quality and Education unit to ensure proper education and training of clinical research staff, develop role-based curricula, and ensure compliance with clinical and regulatory standards.

Required Qualifications

  • Bachelor's degree in a health-related field.
  • Minimum of eight (8) years of experience in clinical research, with at least four (4) years focused on clinical trial operations.
  • Three (3) years of supervisory experience in clinical research.
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