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Clinical Operations Manager / Lead - PSICRO

  • חברה: PSICRO
  • מיקום: Ra'anana

תיאור המשרה

Office-Based in Ra'anana, Israel

We're on the lookout for a knowledgeable, proactive and dedicated person to support and develop our Clinical Operations team in Israel.

The scope of responsibilities will include:

  • Support line management of Clinical Operations staff
  • Management of multiple aspects of clinical research from business development to project execution
  • Coordination of resource allocation to projects and utilization monitoring
  • Oversight of the staff workload, support performance appraisal and career development
  • Training, coaching and mentoring the team
  • Involved in hiring, onboarding and integrating of new Clinical Operations’ employees
  • Ensuring compliance with GCP standards and internal/external procedures
  • Development and implementation of quality control
  • Regional project oversight
  • Maintenance, revision and establishment of processes on the regional level
  • Ensuring smooth operation from Study Startup to Study Close out stages
  • Communication point to investigators, regulatory and ethics authorities, clients and vendors for various project-related matters 

על התפקיד

We offer:

  • Excellent working conditions
  • Extensive training and friendly team
  • Competitive salary and benefits package
  • Opportunities for personal and professional growth

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

תחומי אחריות

Support line management of Clinical Operations staff Management of multiple aspects of clinical research from business development to project execution Coordination of resource allocation to projects and utilization monitoring Oversight of the staff workload, support performance appraisal and career development Training, coaching and mentoring the team Involved in hiring, onboarding and integrating of new Clinical Operations’ employees Ensuring compliance with GCP standards and internal/external procedures Development and implementation of quality control Regional project oversight Maintenance, revision and establishment of processes on the regional level Ensuring smooth operation from Study Startup to Study Close out stages Communication point to investigators, regulatory and ethics authorities, clients and vendors for various project-related matters

דרישות

  • College or University degree in Life Sciences
  • Demonstrated operations experience in a CRO (preferable), or a pharma company
  • Experience with clinical research sites, study logistics, legal, regulatory and ethics in Israel
  • Experience in all study phases in Israel (preferable)
  • At least 2 years’ experience in clinical team supervision including Remote team staff
  • Excellent English and Hebrew
  • Ability to travel internationally
  • Strong time management, organizational, leadership, planning and presentation skills, result-oriented approach

Company Description

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.