Clinical Consultant

The Clinical Consultant coordinates both the clinical teams with any process support for future trial coordination with patients and their medical team. This includes tasks like study set up, participant (patient) recruitment, data collection and management, regulatory compliance and some aspects of data analysis and reporting. Respond to patient requests for compassionate use of Providence’s vaccine products.

Prior industry experience is valuable and relies on strong organizational skills, good attention to detail, and a willingness to follow established procedures while learning about preclinical & clinical workflows in a regulated environment.

How we plan on keeping you busy:

• Protocol preparation:
  • Participates in study design, protocol development and execution of clinical research in the field of cancer and infectious diseases
  • Contributes to the overall medical strategy of the clinical development plan of cancer therapeutics and vaccines. Gives as needed in-depth medical input on potential risk and regulatory compliance.
• Study Setup and management:
  • Assists with the development of case report forms, perform medical monitoring, liaise with investigators and site personnel, perform preliminary and exploratory data analyses on clinical trials, author clinical study reports, provide input on publication materials.
• Data collection and management:
  • Collecting, managing, and documenting study data accurately and efficiently, ensuring data integrity and adherence to protocols
  • Regulatory Compliance Maintaining meticulous records and ensuring compliance with all applicable regulatory requirements, including those of the Institutional Review Board (IRB) and other relevant authorities
• Communication and collaboration:
  • Maintaining clear and consistent communication with principal investigators, sponsors, and other research team members, as well as with any relevant regulatory bodies
• Study monitoring and safety:
  • Monitoring study progress, participant safety, and adherence to the protocol, and reporting any adverse events or protocol deviations promptly. Oversee these activities with stake holders

What will help you get here:

• Minimum 10 years experience overseeing clinical trial(s)
• Have strong knowledge of early clinical development (phase I/II) and clinical trial requirements from First in Human to Phase III studies
• Have the ability to represent Providence in a variety of internal and external settings
• Possess strong interpersonal, analytical and presentation skills
• Demonstrate success in teamwork within a multifunctional organization and ability to inspire trust among colleagues
• Maintain close attention to detail and the ability to anticipate and mitigate problems
• Be innovative, flexible, resilient, and visionary with the ability to seize opportunities
• Can prioritize, respond to directives, and work in a fast-paced and dynamic environment

Working Conditions:

• Role is based in Calgary, Alberta, with a Flexible work schedule
• Hybrid work model, with ability to travel globally to support ongoing trials & patients
• This is a contract / part time position to start to assess long term requirements

What it’s like to work with us:

At Providence Therapeutics, you’ll be working with a clinical Canadian Biotech company that is innovating in the fast-growing mRNA space.   We are focused on helping and healing people around the world. We are looking for culture builders and visionaries to help us make our infectious disease and cancer programs a reality. You truly have an opportunity to have a positive impact on individuals’ lives.

What you can expect working with us:

• Competitive salary
• Flexible and Remote Work