ICON plc este o organizație globală de cercetare în regim contractual, care deservește industriile din domeniul sănătății și farmaceutic. Activitatea sa cuprinde servicii clinice, de consultanță și comerciale care sprijină dezvoltarea medicamentelor, de la cercetarea timpurie până la activitățile post-comercializare. Compania oferă soluții precum studii clinice descentralizate, evaluarea siguranței cardiace, laboratoare clinice pentru etapele timpurii, imagistică medicală, informații de reglementare și dovezi din lumea reală. ICON plc dispune, de asemenea, de expertiză terapeutică în domenii precum bolile cardiovasculare, oncologia, medicina internă, terapiile celulare și genice și medicamentele biosimilare, combinând analiza datelor cu o abordare axată pe pacienți pentru a contribui la avansarea programelor clinice.
Clinical Trial Manager II at ICON plc – Remote in Argentina
Lead clinical trial operations, data review, and regulatory compliance for ICON plc, a global clinical research organization. Coordinate cross-functional teams and study deliverables in a remote role based in Buenos Aires.
Descriere
- Manage clinical trial workstreams and ensure deliverables meet quality and timeline requirements
- Partner with cross-functional teams to plan and execute effective participant enrollment strategies
- Create and implement comprehensive clinical trial protocols with relevant internal teams
- Direct daily clinical trial operations in accordance with applicable regulatory standards
- Review and interpret trial data, identify trends, and recommend ways to improve study outcomes
- Anticipate execution challenges and implement practical solutions to keep trials on track
- Build effective relationships with internal and external stakeholders to support smooth trial delivery
- Balance competing priorities while supporting team development
Cerințe
- Bachelor's degree in a relevant field
- At least [X] years of experience managing clinical trials
- Demonstrated expertise in clinical trial design and execution
- Strong knowledge of applicable regulatory requirements
- Advanced analytical and problem-solving abilities
- Ability to interpret complex medical data
- Clear and effective communication and interpersonal skills
- Ability to work collaboratively across diverse teams
- Strong attention to detail and organizational skills
- Proven ability to manage multiple tasks and competing priorities successfully
- Willingness to travel as needed, approximately 25%
- Legal authorization to work in the country where the role is based
Beneficii
- Competitive base pay with performance-related incentives
- Health and wellbeing programs, including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programs and wellbeing resources
- Structured training and career development opportunities