Senior Global Clinical Trials Manager

Artech Information System LLC; California City (CA); Presencial; USD 100.000 - 130.000; Jornada completa

Descripción de la vacante

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!

Formación

• 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.

Responsabilidades

• 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.

Conocimientos

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

Educación

University degree in Medical Science or equivalent education

Advanced degrees (e.g., MD, PhD, O.D., PharmD)

Descripción del empleo

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!