Associate Regulatory

ResponsibilitiesThe Regulatory Submissions Coordinator will be responsible for providing day-to-day departmental/project support activities, including collection of vital documents for ethics submissions and preparation of study documents.What You'll DoCollaborate with Regulatory Submission Managers and Start Up teams to ensure timely completion of...

Study Start Up Associate II (Regulatory Submissions) - Chile - Hybrid Scheme ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development At ICON, it’s our...

Organizational Relationship(s) including to whom the position reports (JD Job Title): This position reports to the locally based Regional Labeling Head, International Labeling Team Lead, or to a Senior Manager in International Labeling Group. Position Purpose The Hub Labeling Senior Associate level, is responsible for executing the content management of...

Press continue to see content specific to your location. United States Associate Relations Specialist Santiago CLP 20,000,000 - 40,000,000 Job Description: Associate Relations Specialist - Your new challenge @ MARS? Reporting to our Associate Relations Country Lead South LATAM, the AR Specialist will serve as the point of contact for associate...

Job Description: Associate Relations Specialist - Your new challenge @ MARS? Reporting to our Associate Relations Country Lead South LATAM, the AR Specialist will serve as the point of contact for associate relations issues and inquiries for an identified cross-segment, cross-functional client group in South LATAM. Responsibilities include building...

**Job Description**: 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 policies and procedures, quality standards and adverse event reporting requirements internally and...

About the Role:We are seeking a highly motivated individual to join our Pharmacovigilance team as a PV Operational Associate. In this role, you will be responsible for ensuring the day-to-day operations of PV systems across assigned regions meet the required standards. Key responsibilities include developing and maintaining local procedures, participating in...

**Fitch Ratings: Associate Director - Financial Institutions - Chile** Fitch's Financial Institutions group is responsible for the credit ratings of issuers and debt related to (bank and non-bank) financial institutions. **Reporting Structure** **Location** The position is based in Santiago. Some international travel required. **Primary responsibilities...

We're seeking a highly skilled Clinical Research Associate II to join our team in Chile. As a key member of our global organization, you'll contribute to the successful execution of clinical studies by working closely with a close-knit team of CRAs.The ideal candidate will have a strong background in clinical research, with experience in monitoring studies...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives. ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives. ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing...

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 at PSI...

With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. - Performs clinical study site management/monitoring...

**Job Description**: 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 policies and procedures, quality standards and adverse event reporting requirements internally and...

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 policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary...

Senior Study Start Up Associate (Regulatory Submissions) Chile - Hybrid Scheme ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development At ICON, it’s...

Company Description At Visa, your individuality fits right in. Working here gives you an opportunity to impact the world, invest in your career growth, and be part of an inclusive and diverse workplace. We are a global team of disruptors, trailblazers, innovators, and risk-takers who are helping drive economic growth in even the most remote parts of the...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives. ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing...

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...

**Summary**: - Contributes and support the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Supports all registration activities of the Department to ensure compliance with the requisites of the local pharmaceutical regulatory environment. **About the Role**: **Major...