Cro Lead

Job DescriptionIf you are an experienced CRA, who have been mentoring junior staff and/or leading some project activities and feels it's time to take the next step, this opportunity is for you! In the role of Lead CRA, you will manage local CRAs, supervising clinical monitoring and site management activities to verify the protection of trial subjects’...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Must have a Bachelor’s Degree (or equivalent) with 6 - 7 years of relevant healthcare experience including 4 years of monitoring & site management experience. - Managing the cross-functional Country Feasibility team and process, involving the local Monitoring and Site Management and local Medical organizations. A reliable operational feasibility assessment...

**Company Description** We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to...

Job DescriptionTake your career to the next level and be involved in study startup processes in Argentina. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. Hybrid workYou will:Oversee and coordinate the processes critical for clinical trial sites activationCommunicate with project...

Join our team as **Client Services Lead **to serve as the main point of contact for global portfolios, manage the client relationship at the study level, oversee payment management projects and ensure sponsor satisfaction is achieved. Manage and oversee the initiation and study management of protocols including identifying all protocol related information,...

**Trial Preparation, Conduct and Closeout**: 1. Selects sites, conducts and delivers the trial according to the clinical trial protocol, within trial timelines, and in compliance with ICH-GCP, procedures and all other relevant applicable regulations. 2. Perform/supervise local adaptation of the required documents for submission according to the package...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

**Site Name**: Buenos Aires Libertador **Posted Date**: Jun 28 2023 Liderar las actividades operativas, de planeamiento y de entrega de estudios clínicos de fase 1-4 en el país o países asignados; en todas las áreas terapéuticas para estudios de Pharma y de Vacunas, de acuerdo con los estándares de calidad de la compañía y las normas regulatorias...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

The Clinical SAS Programmer will lead the programming activities for various purposes including SAS Data Listings to be used for data review, Safety Review Listings, Centralized Monitoring Listings and Reports. The Clinical SAS Programmer will also be responsible for productions of Key Risk Indicators, working collaboratively across departments to produce...

RESPONSIBILITIES: - Lead strategic direction of the CNS Center of Excellence as the therapeutic area head.- Demonstrate oversight in strategic proposal development in conjunction with leaders of other functions.- Act as consultant to their team members and other IQVIA stakeholders throughout the research and development life cycle and the duration of...

External Job Description IQVIA Biotech is seeking a Senior Site Contracts Associate or Site Contracts Associate located in Argentina: **BASIC FUNCTION**: To manage the review and negotiation of contracts with Investigators participating in clinical research on behalf of pharmaceutical Sponsors. **ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES**: -...