Senior Clinical Trial Manager

Job description

Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our experienced team delivers high-touch services and technology to ensure the safety of all stakeholders across the clinical research community with an emphasis on ethics, compliance, and innovation. Job Title: Senior Clinical Trial Manager Location: Mississauga, Ontario Function: Clinical Operations ESSENTIAL DUTIES AND RESPONSIBILITIES: The Clinical Trial Manager (CTM) will oversee one or more clinical trials and ensure that project milestones are met on time, within budget, and in compliance with best practices. The CTM will also be responsible for maintaining high-quality standards throughout the project. Designing and executing study plans and protocols Managing study budgets Supervising trial sites and the various teams involved in the clinical trial’s operations. Coordinating trial tasks and timelines, ensuring all teams and tasks are on schedule. Ensuring compliance with regulatory requirements Overseeing patient recruitment Collaborating with Project managers to establish targets. Recruiting staff and participants for studies Coordinating communications with regulatory organizations Ensuring safety of all involved parties Ensuring adherence to all protocols and procedures Lead internal clinical operations calls Lead and support on client calls Oversee vendors in support of ongoing clinical trial projects Train and mentor Clinical Trial Managers, Clinical Research Associates, and Clinical Trial Associates EDUCATION AND EXPERIENCE REQUIRED: Bachelors Degree or 6 years relevant experience with a CRO, Biotech, or Pharma Manufacturer At least 3 years in a clinical trial management role Previous experience CRA experience independently monitoring drug trials is highly preferred COMPENSATION & BENEFITS: Sitero proudly offers an impressive compensation package and benefits, including a competitive salary, Variable pay, paid time off, and healthcare and retirement benefits. EMPLOYMENT TYPE: Full Time, Permanent COMMITMENTS: Standard Hours 40 hours per week, one hour lunch, Monday – Friday. Additional hours as needed. Willing to work in shifts as and when needed. In Office 3x per week. Remote from home 2x per week DISCLAIMER: Sitero is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other factors .