About this role
Role Overview
- Support Clinical Study Team to ensure quality and integrity of processes and data generated by external clinical research vendors
- Lead study-level vendor set-up and readiness activities for assigned vendor categories
- Provide technical expertise in one or more areas: Central Lab, eCOA, Medical Imaging, ECG, Home Health Care, Patient Recruitment & Retention, Adjudication
- Provide vendor management expertise to Clinical Study Team for study level vendor strategy and selection support
- Translate the protocol requirements into vendor-facing requirements and specifications
- Ensure vendor set-up documentation is controlled and filed appropriately
- Identify gaps and drive continuous improvement of tools, processes and reporting that strengthen and standardize the study team-vendor interface
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 7+ years of relevant experience in clinical trial management
- Broad clinical research experience (e.g. biotech, pharmaceutical or CRO environment) including experience working in Clinical Research Vendors (CROs, central labs, imaging vendors, eCOA providers etc.)
- Understanding of clinical development process and clinical trial operations
- Knowledge of vendor oversight principles in clinical trials (documentation discipline, quality expectations)
Benefits
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways