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

Worldwide Clinical Trials; Ontario; Remote; CAD 80,000 - 150,000; Full time

Job summary

An established industry player is seeking a Medical Director for their Medical Affairs team, focusing on Neurology and Psychiatry. This full-time role involves collaborating on clinical trial processes, supporting project teams with scientific expertise, and mentoring medical staff. The ideal candidate will have a Medical Degree and experience in a CRO setting, along with strong communication and organizational skills. Join a diverse and inclusive team dedicated to making a difference for patients and caregivers worldwide.

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

Excellent English communication skills

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

1. Collaborate on processing Serious Adverse Events (SAEs)
2. Contribute to clinical development program design and research documentation
3. Support Business Development through proposal and feasibility assessments
4. Review and assist in preparing study reports and documentation
5. Maintain knowledge of therapeutic advances and marketplace developments
6. 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
• Excellent English communication skills
• 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.