Research Services Jobs in Buenos Aires

Job OverviewThe Medical Director will be the medical expert on the IQVIA team working on clinical research trials in neurological diseases and disorders. This involves applying medical and scientific knowledge and expertise in support of the trial. These clinical trials will cover the full range of...

IQVIA HCPN has an exciting position in Argentina for a freelance CRAs. Location: Argentina travel within Argentina requiredFTE: 0.6 FTEContract: FreelanceStart: asapDuration: around 6 monthsTrials: Phase II Ophtalmology Basic Functions:Participates in the preparation and execution of Phase II and II...

Job OverviewClinical Trial Educators (CTEs) - Argentina collaborate with research staff and key stakeholders to enhance trial recruitment and support studyspecific training needs. The CTE serves as a strategic partner to internal and external teams optimizing site experience and performance. This ro...

This Assoc. Medical Director role will provide medical clinical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned trials.Serve as a medical expert during project delivery life-cycle. Provide therapeutic medica...

Job Title: Registered Dietitian Clinical Research SupportLocation: Remote - Argentina (Cordoba)Job Type: Freelance / Part-time (ad hoc hours)Are you ready to make a real impact Do you want to work flexibly from anywhere in Argentina while advancing your career with a global leader in healthcare in...

Make an impact on patient health!IQVIAs Global Site Activation Team of 2000 employees drives best in class site and customer experience with industry leading outcomes.We keep the patient at the forefront; Always Impatient for the Patient and we excel in our collaboration with our external/internal c...

Job OverviewPerform clinical research procedures and support study execution by collecting recording and interpreting data for participants enrolled or being screened for clinical studies. Ensure all activities follow study protocols SOPs and GCP guidelines. Contribute to daily workload planning and...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities resourcing and Functional Service (FSP) solutions.J...

Job OverviewEngage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol standard operating procedures good clinical practice and applicable regulatory requirements.Essential Functions Complete appro...

Job OverviewAccountable for capability and learning activities related to the delivery of CDGM services and the adoption of TMF and good documentation practices across the business.ResponsibilitiesDevelop and implement effective fit-for-purpose capability development learning and knowledge managemen...

Job OverviewManage a team of clinical staff supporting clinical studies. Ensure projects are well-resourced and employees are trained and meeting objectives.Essential FunctionsStaff Management: Plan assign and direct work. Assess performance guide professional development reward and discipline emplo...

QA ManagerFull remote role with occasional travel: 2030% per yearJob OverviewOversee & coordinate assigned QA program in support of customer accounts functional accounts audit and inspection program or QA quality management system at a regional and/or global level. Provide support to management with...

Job OverviewThe Medical Director provides senior medical clinical and scientific leadership across IQVIA projects with a primary focus on Global and Regional Medical Monitoring and medical strategy support. The role serves as a medical expert throughout the project delivery lifecycle ensuring patien...

Job Description Prepares and/or reviews regulatory documents to support clinical trial submissions. With guidance from senior staff provides regulatory support for more complex projects.Acts as a Clinical Trial Regulatory Manager (CTRM) on straightforward projects independently and complex regulator...

The Senior Medical Advisor provides seniorlevel medical and scientific leadership with a strong focus on pharmacovigilance and medical safety while supporting broader medical affairs and evidence activities. The role is responsible for medical review and oversight of safety data across clinical and...

Responsibilities:Provide project management support to the PRE Content Development team for Global Master ICFs eConsents PLS digital toolkits and standalone writing projects (where PRE services are not otherwise scoped).Monitor and triage incoming ICF eConsent and PLS work and contribute to weekly I...

Job OverviewSupports all IQVIA Patient Recruitment and Enablement as a Graphic Designer for print Web or multimedia projects supporting patient recruitment and retention for Global clinical trials.Essential Functions Creates high impact designs illustrations branding and layout to engage attract and...

Role OverviewThis role supports the development of pricing analytics and models that enable informed decisionmaking on customer deals profitability and risk. You will work closely with senior pricing professionals gaining handson experience in Excelbased financial modeling pricing strategy and cross...

Job OverviewPerform a variety of clinical procedures to collect record report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol standard operating procedures (SOPs) and Good Clinical Practice (GCP). Assist with daily workload planning.Ess...

Whether youre beginning or continuing your career as a CRA this role is an ideal stepping-stone. Youll have training and development to plan and progress your career in the direction you choose. And you wont do it alone you will have dedicated mentoring and receive structured quarterly reviews on p...