Senior Local Trial Manager (Sponsor dedicated)

IQVIA LLC; Buenos Aires; Híbrido; ARS 1.800.000 - 3.000.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Home-based benefits

Office in Buenos Aires

Descripción de la vacante

IQVIA LLC is seeking a Senior Local Trial Manager to lead clinical trial delivery in Argentina. You will work with clinical teams to ensure regulatory compliance, recruitment targets, and quality delivery across projects.

The role requires a Bachelors degree in a health-related field and 5 years of clinical research/monitoring experience, with fluency in Spanish and advanced English. Hybrid work in Buenos Aires is available, with both home-based and office components.

Formación

• Bachelors degree in health care or another scientific discipline is required.
• 5 years of clinical research/monitoring experience or an equivalent combination of education and experience.
• Fluency in the local language (Spanish) and advanced English is required.

Responsabilidades

• Lead and deliver clinical trials in Argentina in accordance with ICH-GCP and SOPs.
• Manage clinical team and project plans to meet recruitment targets and milestones.
• Oversee project finances, risk management, and stakeholder communications.

Conocimientos

Advanced English

Spanish

Clinical trial management

Educación

Bachelors degree in health care or science

Descripción del empleo

**Sponsor dedicated - Senior Local Trial Manager** **Job Overview**Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Clinical Lead is a member of the core project team responsible for the clinical delivery of clinical studies to meet contractual requirements in accordance with Standard Operating Procedures (SOPs), policies and practices. Clinical Leads ensure clinical delivery to customers, lead clinical teams and partner with Project Leaders and other functional teams ensuring projects meet delivery requirements at all times.This is a **local trial management** support position, responsible for clinical delivery in **Argentina**. **Essential Functions**• Ensure clinical delivery of assigned projects in compliance with regulatory requirements (International Conference on Harmonization (ICH)-Good Clinical Practice (GCP), protocol), customer requirements (contract), and internal requirements (policies, Standard Operating Procedures (SOPs), project plans).• Accountable for meeting projects’ recruitment targets and ensuring appropriate recruitment strategies are in place.• Contribute to the development of the project risk mitigation plan and manage clinical risks through the project’s lifecycle.• Ensure clinical quality delivery by identifying quality standards/requirements, planning how compliance will be measured, monitoring and overseeing management of clinical quality issues.• Manage clinical aspects of Project Finances including Estimate at Completion (EAC). Understand the scope of clinical delivery and create plans to deliver. Monitor and manage changes against baseline Estimate at Completion (EAC) and identify additional service opportunities or out of scope work.• Identify clinical stakeholder landscape for the project and manage both internal and external stakeholders through effective communication and resolution management.• Collaborate with the clinical team to support milestone achievements. Report to internal and external stakeholders as per project scope requirements.• Resourcing and Talent Planning of the clinical team. Manage the clinical team at project level to successfully deliver the project through the establishment of high-quality operational plans and guidance and project related trainings.• Conduct regular team meetings and communicate appropriately to achieve objectives.• Support professional development by providing feedback to clinical team line managers on performance relative to project tasks.• May contribute to the development of the clinical delivery strategy for proposals. Participate in bid defense preparations and meetings. Develop and present Clinical Operation plan in partnership with Business Development and Project Leadership.• May mentor and coach new peers as they assimilate into this role.• May work as a primary Clinical Lead alongside other Clinical Leads to deliver large, global trials.• May attend site visits as applicable in support of project delivery. **Qualifications**• Bachelor's Degree in health care or other scientific discipline required (graduated, mandatory).• Requires 5 years clinical research/monitoring experience or equivalent combination of education, training and experience (mandatory).• Fluency in the local country language (spoken and written) and **advanced English** is required, tested during the interview process.• Based in **Buenos Aires, Argentina**. Home based benefits and office requirements in Buenos Aires.• Requires basic knowledge of Project management practices and terminology.• Requires good knowledge of applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.• Requires broad protocol knowledge and therapeutic knowledge.• Requires good understanding of Clinical Research industry (drug/device/technology/etc.) and the relevant environments in which it operates.• Requires understanding of project finances.• Knowledge of clinical trials conduct in addition to skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct.• Communication - Strong written and verbal communication skills including good command of English language.• Problem solving - Problem solving skills.• Organization - Planning, time management and prioritization skills.• Prioritization - Ability to handle conflicting priorities.• Quality - Attention to detail and accuracy in work. Results-oriented approach to work delivery and output.• Leadership - Good influencing and negotiation skills. Good judgment and decision-making skills. Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues.• IT skills - Good software and computer skills, including Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.• Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients.• Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.• Effective communication - Ability to influence without authority.• IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.