Medical Director, Medical Affairs - Neurology / Psychiatry - Argentina Remote

Worldwide Clinical Trials; Ontario; Remote; CAD 100,000 - 140,000; Full time

Job summary

An established industry player in clinical research is seeking a Medical Director for their Medical Affairs team, specializing in Neurology and Psychiatry. This full-time role offers the opportunity to lead clinical trial initiatives, mentor medical staff, and collaborate on innovative projects that impact patient care. Join a diverse and inclusive environment where your expertise will contribute to groundbreaking research and therapeutic advancements. If you are passionate about improving lives through clinical excellence and have a strong medical background, this role is perfect for you.

Qualifications

• Minimum 2 years of medical monitoring experience in a CRO setting.
• Valid passport and ability to travel as needed.

Responsibilities

• Collaborate on processing Serious Adverse Events (SAEs).
• Contribute to clinical development program design and research documentation.
• Support Business Development through proposal and feasibility assessments.

Skills

Proficiency in Word

Proficiency in Excel

Proficiency in Access

Strong organizational skills

Strong presentation skills

Education

Medical Degree with a focus on Psychiatry or Neurology

Job description

Medical Director, Medical Affairs - Neurology / Psychiatry - Argentina Remote

Join to apply for the Medical Director, Medical Affairs - Neurology / Psychiatry - Argentina Remote role at Worldwide Clinical Trials

Overview

Worldwide Clinical Trials is a global, midsize CRO dedicated to pioneering innovative approaches to cure persistent diseases. We are a team of over 3,500 experts committed to improving lives through our work in clinical research.

Our Culture and Mission

We foster a diverse and inclusive environment that promotes collaboration, creativity, and excellence. Our mission is to work passionately to make a difference for patients and caregivers worldwide.

Role of Medical Affairs

Medical Affairs is integral throughout the clinical trial lifecycle, supporting project teams with scientific and medical expertise. The team collaborates closely with other departments and engages in activities such as protocol development, medical monitoring, pharmacovigilance, and medical writing.

Key Responsibilities

• Collaborate on processing Serious Adverse Events (SAEs)
• Contribute to clinical development program design and research documentation
• Support Business Development through proposal and feasibility assessments
• Review and assist in preparing study reports and documentation
• Maintain knowledge of therapeutic advances and marketplace developments
• Mentor medical staff and uphold high work ethics

Qualifications

• Medical Degree with a focus on Psychiatry or Neurology
• Minimum 2 years of medical monitoring experience in a CRO setting
• Valid passport and ability to travel as needed

Skills

• Proficiency in Word, Excel, Access
• Strong organizational and presentation skills

Additional Information

This is a full-time, mid-senior level position. We value diversity and are committed to equal opportunity employment.