Senior Clinical Trial Manager

Sitero LLC

$90K — $120K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree or 6 years of relevant experience in CRO, Biotech, or Pharma
  • Minimum 3 years in a clinical trial management role
  • Preferred previous CRA experience with independent drug trial monitoring

Responsibilities

  • Design and execute clinical study plans and protocols
  • Manage study budgets and oversee trial sites
  • Coordinate timelines and tasks across teams
  • Ensure compliance with regulatory requirements
  • Oversee patient recruitment and study participant selection
  • Facilitate internal and client communications regarding trials
  • Train and mentor junior clinical staff

Benefits

  • Competitive salary
  • Variable pay
  • Paid time off
  • Healthcare benefits
  • Retirement benefits
Full Job Description
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

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