Intern - Clinical Research (Regulatory & Contracts)

Job Summary: The Clinical Research Associate at Medpace is offering the unique opportunity to have an **exciting career** in the research of drug and medical device development. For those with **medical and/or health/life science interest and background** who want to explore the research field, **travel throughout Brazil**, and be part of a team bringing...

**Principal Clinical Research Associate** **Please submit your CV in English for Quickest Review Process!** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or...

**Company Description** Describe the primary goals, objectives or functions or outputs of this position. To enable AbbVie’ s emergence as a world class R&D organization, the position anticipates and proactively solves studyrelated clinical site issues as they occur and initiates, recommends and communicates corrective action ensuring successful protocol...

Company Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Clinical Research Associate II at PSI...

This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. COM, Head COMs or CRD, the person is responsible for...

Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest...

**Senior Clinical Research Associate** **(Level dependent on experience)** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or milestone that they have achieved....

Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest...

Hobson Prior is seeking a Clinical Research Coordinator for a full-time, 6-month contract in São Paulo, Brazil. This role involves supporting cardiology studies with a focus on patient visits, data entry, and maintaining regulatory documents. The position requires immediate availability and a commitment of 40 hours per week.Please note that to be considered...

Hobson Prior is seeking a Clinical Research Coordinator for a full-time, 6-month contract in São Paulo, Brazil. This role involves supporting cardiology studies with a focus on patient visits, data entry, and maintaining regulatory documents. The position requires immediate availability and a commitment of 40 hours per week. Please note that to be...

Hobson Prior is seeking a Clinical Research Coordinator for a full-time, 6-month contract in São Paulo, Brazil. This role involves supporting cardiology studies with a focus on patient visits, data entry, and maintaining regulatory documents. The position requires immediate availability and a commitment of 40 hours per week.Please note that to be considered...

At ICON plc, a world-leading healthcare intelligence and clinical research organization, we're proud to foster an inclusive environment driving innovation and excellence. Our mission is to shape the future of clinical development, and we're seeking a skilled Clinical Trial Administrator to join our diverse and dynamic team.We offer a competitive salary range...

**Responsibilities include, but are not limited to**: - The role is accountable for performance and compliance for assigned protocols and sites in a country; - Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event...

Essential Functions - Provide clinical research support to investigators and site staff, including - Verify and/or correct research study information on source documents; research queries and variances; and provide feedback to the site data collector. - Input research study data into trial Electronic Data Capture (EDC) system, maintaining quality control...

The Ass CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and country regulations. The position has a significant impact on how a country can deliver...

About FortreaFortrea is a leading global contract research organization that prioritizes scientific rigor and has extensive experience in clinical development. The company provides a wide range of clinical development, patient access, and technology solutions across over 20 therapeutic areas to pharmaceutical, biotechnology, and medical device customers.With...

This role is accountable for performance and compliance for assigned protocols in a country in compliance and regulations, policies and procedures, quality standards and adverse event reporting requirements internally and externally. The person is responsible for budget/finance aspects, for execution and oversight of clinical trial country submissions and...

**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...

Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine **Main Responsabilities**: Develops strong site relationships and ensures...

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...