30 Ofertas de Kpmg Argentina en Argentina

**CRA 2 - Homebased**
This role is an ideal stepping-stone. You'll have training and development to plan and progress your career in the direction you choose. And you won't do it alone - you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.
Award winning and innovative, we'll give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You'll be building a smart and flexible career with no limits.
While projects vary, your typical responsibilities might include:
+ Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
+ Supporting the development of a subject recruitment plan
+ Establishing regular lines of communication plus administering protocol and related study training to assigned sites
+ Evaluating the quality and integrity of site practices - escalating quality issues as appropriate
+ Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
+ You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.
**REQUIREMENTS**
You should have:
+ A Bachelor's degree in a health care or other scientific discipline or educational equivalent
+ At least 2 years of on-site monitoring experience (Mandatory)
+ Advanced in English.
+ Availability to travel (50% of time)
+ Located in Buenos Aires, Argentina.
+ _Alternatively, you should have an equivalent combination of education, training and experience_
If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team.
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 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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

IQVIA HCPN has an exciting position in Argentina for a freelance CRAs.
**Location: Argentina, travel within Argentina required**
**FTE: 0.6 FTE**
**Contract: Freelance**
**Start: asap**
**Duration: around 6 months**
**Trials: Phase II Ophtalmology**
**Basic Functions:**
Participates in the preparation and execution of Phase II and III clinical trials in Oncology. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements.
**Responsibilities**
+ Participates in the investigator recruitment process, performing site evaluation visits of potential investigators to evaluate the capability of the site to successfully manage and conduct the clinical study.
+ Coordinate activities with the site and internal departments in preparation for the initiation of the study. Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF and EDC system; monitoring activities and study close-out activities.
+ Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISS.
+ Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs.
+ Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory.
+ Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification and works with sites to resolve data queries and produce robust data.
+ May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA.
+ Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.
+ Assists with, and attends, Investigator Meetings for assigned studies.
+ Attends study-related, company, departmental, and external meetings, as required.
+ Ensures all study deliverables are completed per IQVIA Biotech and study timelines
+ Conducts Field Evaluation Visits and field training of CRA Is, IIs and other Sr. CRAs.
+ Serves as mentor for junior CRAs and those new to the company and/or study.
**KNOWLEDGE, SKILLS AND ABILITIES:**
+ Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology.
+ **Minimum of 2 years experience as a CRA and monitoring**
+ Experience in monitoring and/or coordinating clinical trials required.
+ **Ophtalmology experienced needed**
+ **Phase II experience needed**
+ Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
+ Able to form productive professional relationships both internally within own function, cross-functionally and externally with health care professionals.
+ Able to handle several priorities within multiple, complex trials.
+ Able to reason independently and recommend specific solutions in clinical settings.
+ Able to work independently, prioritize, and work within a matrix team environment.
+ Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research.
+ Fluent Spanish language skills
+ Willing to travel exensively within Argentina (Buenos Aires, Salta, Mendoza, Santa Fe, Cordoba)
If this role sounds of interest, please apply today!
\#LI-DNP
\#LI-CES
\#LI-HCPN
\#LI-NS1
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 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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**_IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring in any of the following therapeutics: oncology, cardiovascular or internal medicine:_**
_IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster._
**Job Overview**
We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the successful execution of clinical trials. In this position, you will be responsible for monitoring and managing clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations. Your work will directly contribute to the integrity and quality of clinical research data.
**Key Responsibilities**
+ Conduct all types of site visits-selection, initiation, monitoring, and close-out in alignment with the contracted scope of work, Good Clinical Practice (GCP), and ICH guidelines.
+ Collaborate with site staff to implement and track subject recruitment strategies that align with project timelines and enrollment goals.
+ Deliver protocol and study-specific training to site personnel and maintain consistent communication to manage expectations and resolve issues.
+ Assess site performance and adherence to the protocol, escalating quality concerns as needed to ensure compliance and data integrity.
+ Monitor study progress by tracking regulatory submissions, subject enrollment, case report form (CRF) completion, and resolution of data queries.
+ Ensure that essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site File (ISF) in accordance with regulatory standards.
+ Document site management activities, visit outcomes, and follow-up actions through detailed reports and correspondence.
+ Work closely with cross-functional project teams to support study execution and ensure alignment with project goals.
+ Depending on the project, you may also support site-level recruitment planning and financial management, including invoice collection and budget tracking.
**Qualifications**
+ Bachelor's degree in life sciences or health-related field (or equivalent experience).
+ Requires at least 1 year of on-site monitoring experience.
+ Strong understanding of GCP, ICH guidelines, and regulatory requirements.
+ Ability to travel as required by the project.
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 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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**¿Quiénes somos?**
WSP es una de las principales firmas de consultoría e ingeniería del mundo. Proporcionamos servicios profesionales en las áreas de transporte e infraestructura, edificación, medio ambiente, energía, recursos y sostenibilidad. Nos impulsa una visión clara: convertirnos en líderes globales en nuestro sector, brindando soluciones innovadoras y sostenibles que aporten valor a nuestros clientes y comunidades.
Contamos con una red global de expertos que colaboran para resolver los desafíos más complejos, combinando conocimiento técnico, excelencia operativa y un fuerte compromiso con la seguridad, la ética y la sostenibilidad.
**¿Por qué trabajar en WSP?**
En WSP fomentamos una cultura diversa e inclusiva donde las personas son el centro de nuestro negocio. Promovemos el desarrollo profesional, el aprendizaje continuo y la colaboración en un entorno dinámico y desafiante.
Valoramos el talento, la innovación y el trabajo en equipo, ofreciendo oportunidades para participar en proyectos relevantes a nivel nacional e internacional.
En WSP fomentamos activamente las postulaciones de personas calificadas y elegibles, independientemente de su sexo, raza, discapacidad, edad, orientación sexual, identidad o reasignación de género, religión o creencias, estado civil, embarazo o maternidad/paternidad.
**¿Estás listo para empezar?**
_Con nosotros puedes._
**Sobre esta oportunidad:**
Nos encontramos en búsqueda de un **Prevencionista de Riesgos / HSE** en Terreno para integrarse a nuestro equipo WSP en Argentina.
El cargo tiene base en la Provincia de Río Negro.
El objetivo del cargo es supervisar y controlar el cumplimiento de estándares HSE en obra, asegurando condiciones seguras de operación y el cumplimiento de normativas y exigencias del cliente, con un enfoque fiscalizador en terreno.
**Responsabilidades:**
- Supervisar y controlar el cumplimiento de estándares HSE en obra por parte de contratistas y subcontratistas.
- Verificar en terreno el cumplimiento de normativas legales vigentes y requerimientos del cliente.
- Realizar inspecciones, auditorías en terreno y seguimiento sistemático de condiciones operativas.
- Emitir observaciones, gestionar desvíos y asegurar la implementación de acciones correctivas.
- Intervenir técnicamente ante situaciones de riesgo, incluyendo la detención de trabajos cuando corresponda.
- Gestionar la documentación HSE de contratistas, asegurando trazabilidad y cumplimiento.
- Coordinar con equipo de proyecto, clientes y contratistas para asegurar estándares de seguridad.
- Identificar, evaluar y priorizar riesgos operacionales en terreno.
**Requisitos:**
- Formación mínima como Técnico en Higiene y Seguridad (excluyente).
- Deseable formación universitaria como Licenciado/a en Higiene, Seguridad o carrera afín.
- Experiencia entre 8 a 10 años en proyectos de construcción, minería y/o petróleo.
- Matrícula profesional vigente, o condición necesaria para gestionar su matriculación en la provincia de Río Negro en el corto plazo.
- Experiencia en control de contratistas en terreno.
- Conocimiento en gestión de documentación HSE.
- Experiencia en identificación y evaluación de riesgos (IPER, ATS y permisos de trabajo).
- Manejo de herramientas de Microsoft Office.
- Licencia de conducir vigente y experiencia en conducción en terreno, idealmente en vehículos 4x4.
- Disponibilidad para trabajo en terreno en condiciones geográficas y climáticas variables.
**¿Qué te ofrecemos?**
- Ser parte de una compañía global con proyectos desafiantes y de alto impacto.
- Ambiente de trabajo colaborativo y oportunidades de desarrollo profesional.
- Participación en proyectos relevantes a nivel regional.
- Acceso a capacitación continua y aprendizaje en equipos multidisciplinarios.
\#LI-VVB
\#Argentina
**Title:** *Prevencionista de Riesgos / Terreno Argentina*
**Location:** *ARG-Mendoza*
**Requisition ID:** * *

**Snapshot de la Posición**
Ubicación: Córdoba, Argentina
Área: Ventas
Negocio: Alimentos & Bebidas
Tipo de contratación: Full time permanente
**Resumen de posición**
Serás responsable de contribuir a la planificación e implementación de las principales actividades que son input para el Plan Anual del Cliente y su respectiva contribución a las estrategias de cada uno de las categorías y negocios.
**Un día en la vida de.**
- Desarrollar y expandir el canal Distribuidores exclusivos de Nestle dentro de la región centro (Córdoba, San Luis, La Rioja y Catamarca) brindando soporte a la fuerza de venta de los mismos generando nuevas oportunidades de venta específicamente en: Autoservicios, almacenes y kioscos.
- Ejecutar las estrategias y planes para el cliente alineados con los requisitos de los diferentes negocios (A&B, NIN, NHS).
- Ejecutar en tiempo y forma las promociones y actividades tanto del cliente como al consumidor. Gestionar con los interlocutores indicados para que los procesos fluyan.
- Colaborar con las diferentes áreas asegurando la correcta alineación y mayor eficiencia en la operación.
- Ejecutar las actividades definidas para la mejora continua en aquellos procesos en que participa el cliente. Involucrarse y aportar inputs en el proceso de búsqueda de eficiencias.
- Analizar las principales variables comerciales.
- Diseño y evaluación de la red de distribuidores optimizando ruteos y mapas.
- Armado de forecast y seguimiento del plan anual.
- Capacitación de fuerza de ventas y acciones en PDV. Participación de matinales.
- Activar y desarrollar la cartera de clientes. Crecer en Clientes con Compra.
- Realizar las cobranzas en tiempo y forma.
**Lo que te hará exitoso.**
- Estudios universitarios finalizados o en curso en carreras de Administración de Empresas, Comercialización, Marketing o afines.
- Mínimo 3 años de experiencia en posiciones similares como ejecutivo de cuenta. Idealmente en empresas de consumo masivo y con recorrido en canal distribuidores.
- Perfil con habilidades fuertes en negociación, manejo interpersonal asertivo, marcada planificación y excluyente haber trabajado por objetivos.
- Manejo de Paquete Office ( PPT, Excel avanzado). Ideal contar con experiencia en herramientas digitales comerciales.
- EXCLUYENTE vivir en Córdoba, Argentina.
- Movilidad propia EXCLUYENTE.
- Nivel intermedio de inglés.
**Beneficios**
Importantes descuentos en productos Nestlé y beneficios Purina (descuento y asesoramiento veterinario).
Viernes Flexible: disfrutá de tu semana con un viernes más corto.
Licencias extendidas: creemos que el balance de vida es importante, por eso queremos que estes con tu familia en los momentos más importantes.
Día de cumpleaños
Cobertura médica para vos y tu grupo familiar
Plataforma interna con multiplicidad de capacitaciones para que puedas seguir con tu formación (Grow).
Y muchos beneficios más para que sigas creciendo en Nestlé.

**¿Quiénes somos?**
WSP es una de las principales firmas de consultoría y servicios profesionales del mundo, dedicada a la ingeniería y el diseño, con presencia global. Trabajamos junto a nuestros clientes para desarrollar soluciones sostenibles que contribuyan al crecimiento de las comunidades y la protección del medio ambiente.
**¿Por qué trabajar en WSP?**
En WSP fomentamos una cultura de colaboración e inclusión, donde valoramos la diversidad de pensamientos, experiencias y perspectivas. Promovemos un entorno de trabajo respetuoso, seguro y desafiante, donde cada persona puede desarrollarse profesionalmente y aportar con su talento.
En WSP fomentamos activamente las postulaciones de personas calificadas y elegibles, independientemente de su sexo, raza, discapacidad, edad, orientación sexual, identidad o reasignación de género, religión o creencias, estado civil, embarazo o maternidad/paternidad.
**¿Estás listo para empezar?**
_Con nosotros puedes._
**Sobre esta oportunidad:**
Para WSP en Latinoamérica, nos encontramos en búsqueda de un **Hidrogeólogo Senior** para integrarse al equipo de Aguas, participando en proyectos mineros de alta complejidad a nivel regional, con fuerte foco en Argentina.
El rol tendrá énfasis en análisis en gabinete, interpretación hidrogeológica avanzada y desarrollo de modelos conceptuales y numéricos, apoyando estudios ambientales, operacionales y de cierre de faenas.
**Responsabilidades:**
- Desarrollo e interpretación de modelos hidrogeológicos conceptuales y numéricos.
- Análisis técnico e integración de información hidrogeológica compleja.
- Elaboración de informes técnicos para clientes y procesos regulatorios.
- Evaluación de interacción mina-acuífero y gestión de aguas subterráneas.
- Participación en estudios de drenaje de rajos, relaves y botaderos.
**Requisitos:**
- Formación profesional en Geología, Hidrogeología o carrera afín.
- Experiencia senior en hidrogeología aplicada.
- Alta capacidad analítica y de interpretación técnica.
- Experiencia comprobable en modelación hidrogeológica aplicada a minería.
- Desarrollo o validación de modelos numéricos (MODFLOW, FEFLOW u otros).
- Interpretación técnica de datos hidrogeológicos y ensayos hidráulicos.
- Participación en proyectos mineros o ambientales complejos.
- Experiencia en elaboración de informes técnicos especializados.
- Disponibilidad para participar en proyectos regionales y actividades de terreno cuando sea requerido.
**¿Qué te ofrecemos?**
Formar parte de una compañía global líder en ingeniería y consultoría, participando en proyectos desafiantes y de alto impacto en la industria minera.
Ofrecemos un entorno de trabajo colaborativo, oportunidades de desarrollo profesional y acceso a capacitación continua, junto con la posibilidad de integrarte a equipos multidisciplinarios de alto nivel que impulsan soluciones innovadoras y sostenibles.
\#LI-VVB
\#Argentina
**Title:** *Hidrogeólogo Senior / Argentina*
**Location:** *ARG-Mendoza*
**Other Locations:** *CO-CU-Bogotá D.C.*
**Requisition ID:** * *

**Together, We Change Lives**
At Kelly, we believe the impact of the right person in the right role is limitless. That impact starts with strong recruiting partnerships - and we're looking for an experienced recruiter to help drive hiring success for one of our global manufacturing clients.
We are hiring a **Recruiter** to support a multinational client with a strong presence in LATAM. This is a **fully remote contractor role** intended for long term. This opportunity is ideal for a seasoned recruiter who thrives in a structured, process-driven environment, enjoys partnering closely with hiring leaders, and is confident managing multiple requisitions in a fast-paced, global RPO model.
**What You'll Do**
+ Own full-cycle recruiting for approximately **10-20 requisitions** at a time across manufacturing, operations, and corporate functions
+ Partner closely with hiring managers to understand workforce needs, timelines, and hiring priorities
+ Proactively source, screen, and present qualified candidates across the **LATAM market**
+ Manage interview coordination, candidate communication, and offer processes end-to-end
+ Ensure adherence to RPO workflows, compliance requirements, and documentation standards
+ Provide clear, data-driven updates to hiring leaders and talent stakeholders
+ Act as a trusted recruiting partner while delivering a high-touch, white-glove candidate experience
**What You'll Need**
+ **5+ years of recruiting experience** , ideally within RPO, staffing agency, or global TA environments
+ Proven experience recruiting for technical, professional, and managerial roles
+ Fluency in **English** (required)
+ Experience supporting the broader LATAM market knowledge strongly preferred
+ Ability to manage multiple priorities while meeting deadlines and SLAs
+ Highly detail-oriented, process-driven, and comfortable working within structured systems
+ Strong stakeholder management and candidate communication skills
+ Be located in Argentina, preferably in the Neuquen province
Total compensation package including benefits as applicable to the position - understanding that each person has unique professional and personal needs focused on your total well-being.  Explore our range of benefits at: Kelly Services | People Regular Staff ( is an equal opportunity employer committed to employing a diverse, equitable and inclusive workforce, including, but not limited to, race, gender, individuals with disabilities, protected veterans, sexual orientation, and gender identity. Equal Employment Opportunity is The Law.

**Job Overview**
Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA's suite of solutions to drive operational excellence and strategic leadership with our customers.
**Essential Functions**
- Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.
- May be responsible for delivery and management of smaller, less complex, regional studies.
- Develop integrated study management plans with the core project team.
- Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
- Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
- Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
- Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.
- Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.
- Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.
- May serve as primary or backup project contact with customer and would then own the relationship with the project's key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.;
- Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;
- Ensure the financial success of the project.
- Forecast and identify opportunities to accelerate activities to bring revenue forward.
- Identify changes in scope and manage change control process as necessary.
- Identify lessons learned and implement best practices.
- May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;
- Adopt corporate initiatives and changes and serve as a change advocate when necessary.
- Provide input to line managers of their project team members' performance relative to project tasks.
- Support staff development and mentor less experienced project team members on assigned projects to support their professional development.;
**Qualifications**
- Bachelor's Degree Life sciences or related field.
- Around 6 years of experience in clinical research/project management. Minimum of **3 years in a Project Manager role in a CRO or pharma company.**
- Experience managing projects in these therapeutic areas: **respiratory, ophthalmology, dermatology, rare diseases.**
- Communication - Strong written and verbal communication skills including **good command of English language** . Strong presentation skills.
- Leadership - Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.
- Finances - Good understanding of project financials including experience managing, contractual obligations and implications.
\#LI-NRJ#LI-Remote
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 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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled

**Together We Change Lives**
Kelly is a team of experts driven by our belief that the impact of the right person in the right job is limitless.
No matter where you are in your career journey, you can apply your knowledge and passion to move people, organizations, and communities forward. You'll have opportunities to grow your expertise and capabilities-both professionally and personally. As a team, we celebrate inclusion, caring, and collaboration. As a company, we value integrity and always put people first-so your impact really will change lives.
**About the Role**
Our Recruiter supports internal talent acquisition across the Americas, partnering closely with hiring managers and Talent Acquisition leaders to deliver high-quality talent in a fast-paced, high-volume environment.
This is a fully remote role that focuses on full-cycle recruiting, including sourcing, screening, outreach, and offer management, with a strong emphasis on delivering an exceptional candidate experience. You'll play a key role in hiring across a broad range of profiles, including Account Executives (Sales) and corporate functions supporting the U.S.
**Our Recruiter is accountable for:**
+ Leading full-cycle recruiting from initial outreach through offer acceptance
+ Managing a high-volume requisition load while maintaining quality and speed
+ Building proactive sourcing strategies to engage both active and passive talent
+ Conducting structured candidate screens via phone and video to assess skills and fit
+ Driving outbound engagement through calling, messaging, and email outreach
+ Presenting and managing offers, including candidate communication and negotiation support
+ Partnering with hiring managers and TA leadership to align on hiring needs and priorities
+ Delivering a consistent, positive, and engaging candidate experience throughout the process
+ Maintaining accurate documentation and activity tracking within ATS systems (Avature, Workday, or similar)
+ Identifying opportunities to improve sourcing strategies and overall recruiting effectiveness
**Essential Skills, Knowledge & Experience**
+ Minimum of 2 years of full-cycle recruiting experience required
+ Proven experience in high-volume recruiting environments (required)
+ Experience across multiple industries such as light industrial, manufacturing, and/or staffing preferred
+ Strong candidate-facing experience with the ability to manage full-cycle recruiting end-to-end
+ Experience recruiting across the continental United States
+ Proven ability to source and engage passive candidates and build strong pipelines
+ Strong communicationand relationship-building skills
+ Experience with ATS platforms and sourcing tools (Avature, Workday, or similar)
+ Ability to manage multiple priorities in a fast-paced environment
+ High attention to detail with a strong focus on accuracy and compliance
+ English professional proficiency
**Compensation & Benefits**
Final compensation will be based on experience and geographic location.
Kelly is an equal opportunity employer committed to building a diverse, equitable, and inclusive workforce, including individuals of all races, genders, abilities, protected veteran status, sexual orientations, and gender identities. Equal Employment Opportunity is The Law.