Clinical Trials Account Lead

Cadent is seeking a results-oriented professional to serve as the primary contact for multiple high-level projects supporting digital products in clinical trials. You will foster strong client relationships, oversee delivery timelines and budgets, and collaborate with sponsors, study teams, and cross-functional stakeholders to ensure successful study...

Cadent, a unit within Syneos Health, seeks a seasoned project manager to lead client relationships for multiple accounts supporting digital clinical-trial products. You will coordinate cross-functional teams, ensure timely delivery, onboarding, deployment, and sustained success while monitoring timelines and budgets to optimize outcomes. You will work with...

IQVIA is seeking an Associate Project Lead to join our clinical trial delivery team. You will liaise with clinical teams to accelerate drug development, contribute to study management plans, and serve as primary vendor contact on assigned studies. You will drive delivery quality, timelines, and cost efficiency while ensuring adherence to SOPs and...

IQVIA Biotech in Argentina is seeking a Sr. Site Contracts Associate with 3–5 years of experience in negotiating clinical site contracts and budgets.You will develop the global contracting strategy and support start-up contracting activities for selected sponsors, studies or multi-protocol programs, ensuring alignment with sponsor requirements....

We’re expanding our capabilities across Latin America, and we’re hiring a Senior Clinical Research Associate to support critical studies across Argentina! As a Senior CRA you'll posses a wide-ranging and broad experience handling our most complex and advanced assignments. Responsibilities will be dependent upon the type and timing of the program to...

Milestone One in Mendoza, Argentina seeks a Site Coordinator to support trial sites under ICH-GCP guidelines. You will act as the main liaison between sponsors and sites, coordinate monitoring visits, and track enrollment within defined timelines. The role requires a Life Science degree and at least 3 years in clinical trials, with strong English,...

Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment goals. In this role you will: Actas the main line of communication between the Sponsor or CRO and the site. Ensureresponse to feasibility questions are provided in due time. ...

Milestone One Site Coordinator supports trial sites in all related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment goals. In this role you will: Actas the main line of communication between the Sponsor or CRO and the site. Ensureresponse to feasibility questions are provided in due time. ...

Descripción Del Trabajo At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely...