Senior Clinical Research Associate

Job SummaryAs a Clinical Research Associate Lead at PSI, you will oversee local Monitors, supervising clinical monitoring and site management activities to ensure the protection of trial subjects' rights, safety, and well-being, data quality, and study compliance on a country/regional level.Key ResponsibilitiesFacilitate regional projects as Lead Monitor and...

Job Title: Clinical Research Associate Lead About PSI:We are a leading provider of clinical research services, dedicated to advancing the field of medicine through high-quality research. Salary:$80,000 - $110,000 per annum, depending on experience Job Description:As a Clinical Research Associate Lead, you will be responsible for overseeing the management...

Job Summary:The Clinical Research Associate will be responsible for performing and coordinating all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations, and PPD SOPs.Key Responsibilities:Conduct site visits to assess protocol and regulatory compliance and manage required...

Lead Clinical Research AssociateAbout PSI:PSI is a dynamic organization dedicated to advancing clinical research. Our team of experts works together to deliver high-quality projects and services to our clients.Salary Range: $70,000 - $90,000 per year, depending on experience and qualifications.Job Description:Role Overview:The Lead Clinical Research...

About the Role:We are seeking a highly skilled Clinical Research Associate to join our team at Thermo Fisher Scientific. As a key member of our clinical operations team, you will play a vital role in ensuring the successful delivery of clinical trials.Job Summary:The Clinical Research Associate will be responsible for coordinating and conducting site...

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations,Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts...

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

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

At Merck Gruppe - Msd Sharp & Dohme, we are seeking an experienced Senior Clinical Research Associate to join our team. This is a challenging role that requires strong site management skills and the ability to work independently across multiple protocols, sites, and therapy areas.About the Role:This position is responsible for performing clinical study site...

Job Description OverviewThe Merck Gruppe - MSD Sharp & Dohme is seeking an experienced Clinical Research Associate to join our team as a Clinical Research Site Manager - Senior. As a key member of our global clinical operations team, you will be responsible for managing and overseeing the execution of clinical trials at assigned sites.Key...

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 or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, Company policies and procedures, quality standards and adverse event reporting requirements internally...

Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall 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 activities in compliance with ICH-GCP,...

**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...

**Job Title:** Clinical Research Lead**Job Type:** Full-time**Location:** Colombia**About Psi Cro:We are a dynamic and rapidly growing company in the clinical research industry. Our commitment to employee development and growth is unmatched.**Salary:** $55,000 - $65,000 per year, depending on experience.Job Description:**Company Overview**: At Psi Cro, we...

Job OverviewIngepsy is a leading global contract research organization (CRO) with a strong passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic...

Merck Gruppe - Msd Sharp & Dohme seeks a Senior Clinical Research Associate with a strong background in site management and monitoring to join our team. This is a key role within the company, requiring a high level of expertise in clinical research, regulations, and compliance.About the RoleThe successful candidate will be responsible for ensuring...

Job OverviewPsi Cro is a dynamic, global company founded in 1995, bringing together over 2,800 driven individuals working on the frontline of medical science.Estimated Salary: $60,000 - $80,000 per yearJob DescriptionWe are seeking a highly organized Clinical Research Coordinator to join our international team. As the primary site contact point, you will be...

About the JobWe are seeking an experienced Clinical Research Project Manager to join our team at MSD. As a key member of our clinical operations team, you will be responsible for managing multiple clinical trials from initiation to close-out.Job Summary:Manage multiple clinical trials from initiation to close-outDevelop and execute project plans, timelines,...

Job OverviewWe are seeking a highly skilled Site Activation Specialist to join our team at IQVIA Argentina. The successful candidate will be responsible for performing tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project...

About PSI CROWe are a global Contract Research Organization (CRO) with a commitment to developing our employees in their careers by providing tailored courses and mentoring. Our dynamic team is looking for an experienced Clinical Research Associate to train and coordinate junior CRAs on site.Job DescriptionHome-based position in Colombia, the role will...