Oversee the clinical portion of the budget to ensure efficient resource allocation.
Develop monitoring plans and tools, ensuring effective study oversight.
Train and mentor Clinical Research Associates (CRAs) to optimize their performance.
Drive enrollment and lead study start-up activities, adhering to timelines.
Review trip reports and implement corrective and preventative action plans when necessary.
Foster productive relationships with Sponsors, vendors, and cross-functional teams.
Requirements
A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.
Bachelor's degree in health, life sciences, or other relevant fields of study.
At least 10+ years of relevant experience in clinical trial management.
Preferred: 2+ years of monitoring experience.
Experience in managing complex or global trials is advantageous.
Preferred: Experience in managing all trial components from start-up to database lock.
Preferred: Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives.
Fluency in English (reading, writing, speaking).
Benefits
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
Clinical Research Nurse Coordinator overseeing complex oncology clinical trials within Duke Cancer Institute. Managing study operations, collaborating with multidisciplinary teams, and maintaining regulatory compliance.
Clinical Research Scientist developing innovative breast cancer therapies at Lilly. Collaborating with cross - functional partners in clinical trial design and execution.
Clinical Research Professional II coordinating research activities at UC College of Medicine. Engaging in patient recruitment and maintaining compliance with research protocols.
Clinical Trial Manager overseeing planning, execution, and completion of clinical trials for ICON PLC. Collaborating with teams and managing site relationships to ensure compliance and successful delivery.
Senior Manager overseeing clinical trials in Late - stage Oncology at Pfizer. Providing scientific oversight and collaborating with clinical operations for successful trial execution.
Senior Manager in Late Stage Oncology ensuring quality and integrity of clinical trial processes at Pfizer. Collaborating with cross - functional teams to support drug development and regulatory submissions.
Principal Scientist at Merck managing clinical research activities in Immunology with focus on late - stage development. Overseeing clinical trials and collaborating with cross - functional teams.
Sr Clinical Trial Manager managing clinical trial oversight and ensuring compliance in Poland. Collaborating across teams to meet project milestones and patient safety standards with a hybrid work model.
Senior Clinical Trial Manager at Genmab managing clinical trials and ensuring compliance with regulatory standards. Developing operational plans and coordinating with stakeholders for successful trial execution.
Senior Manager managing clinical science projects within Regeneron Genetics Medicine. Overseeing clinical trials and contributing to regulatory documentation and compliance.