Senior Global Clinical Trials Manager

Artech Information System LLC

California City (CA)

Sur place

USD 100 000 - 130 000

Plein temps

14 jours+

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Résumé du poste

A leading IT staffing company is seeking a Clinical Trial Manager to lead clinical trials effectively. This role involves overseeing all aspects of trials, from planning to reporting. Ideal candidates should possess a university degree in Medical Science or a related field and over 9 years of clinical research experience. Strong communication and organizational skills are essential for collaboration within cross-functional teams, and a solid understanding of clinical trial regulations is required. Join us to contribute to groundbreaking clinical studies!

Qualifications

  • 9+ years in clinical research or relevant scientific industry experience.
  • Experience in planning and execution of clinical studies across various phases.
  • Solid understanding of the integrated development process of medical devices or pharmaceuticals.

Responsabilités

  • Lead the Clinical Trial Team in planning and conducting clinical trials.
  • Author protocols while ensuring efficient trial conduct with timely reporting.
  • Forecast trial resource needs and manage trial budgets effectively.
  • Contribute to the development of clinical sections of regulatory documents.
  • Ensure quality execution of clinical trials within timeline and budget.

Connaissances

Excellent people and communication skills
Ability to establish clear directions and set stretch objectives
Organizational awareness to operate in a cross-functional team
Solid understanding of clinical trial regulations
Ability to embrace and communicate change
Experience in running clinical studies independently

Formation

University degree in Medical Science or equivalent education
Advanced degrees (e.g., MD, PhD, O.D., PharmD)

Description du poste

A leading IT staffing company is seeking a Clinical Trial Manager to lead clinical trials effectively. This role involves overseeing all aspects of trials, from planning to reporting. Ideal candidates should possess a university degree in Medical Science or a related field and over 9 years of clinical research experience. Strong communication and organizational skills are essential for collaboration within cross-functional teams, and a solid understanding of clinical trial regulations is required. Join us to contribute to groundbreaking clinical studies!
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