Clinical Research Associate, CDC

Job DescriptionWe are seeking a skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in the conduct of clinical trials.The primary responsibilities of this position include:Supporting the organization, management, and execution of projects;Ensuring compliance with Good Clinical Practices...

Our TeamAllergan Aesthetics is a global leader in the medical aesthetics industry, committed to delivering innovative solutions that transform lives. We are driven by our passion for improving patient outcomes and our commitment to excellence in everything we do.About the RoleWe are seeking an experienced Clinical Research Associate to join our team. As a...

Company OverviewAllergan Aesthetics, a leader in the medical aesthetics industry, is dedicated to delivering innovative solutions that transform lives. Our mission is to provide safe and effective products that meet the evolving needs of our customers.About the RoleWe are seeking an experienced Clinical Research Associate to join our team. As a key member of...

About Allergan AestheticsAllergan Aesthetics is a global leader in the medical aesthetics industry, committed to delivering innovative solutions that transform lives. We are driven by our passion for improving patient outcomes and our commitment to excellence in everything we do.Job DescriptionWe are seeking an experienced Clinical Research Associate to join...

About UsAllergan Aesthetics is a global leader in the medical aesthetics industry, committed to delivering innovative solutions that transform lives. We are driven by our passion for improving patient outcomes and our commitment to excellence in everything we do.Job SummaryWe are seeking an experienced Clinical Research Associate to join our team. As a key...

Job OverviewWe are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina.The successful candidate will be responsible for conducting site management activities, including monitoring and maintenance of documentation, as well as providing support in the development of subject recruitment plans. Regular communication with...

Clinical Trials Management ExperienceWe are seeking an experienced Clinical Trials Management Expert to join our team at Innovaderm Research. As a key member of our organization, you will be responsible for managing clinical trials and ensuring their successful delivery.Main ResponsibilitiesManage all phases of clinical trials, from start-up to closure,...

This role offers an exciting opportunity to join a dynamic team and contribute to the success of our clinical trials. The Freelance Regional Clinical Trial Coordinator will support the preparation of Investigator Site Files, maintain the Trial Master File, and ensure timely documentation submissions to regulatory authorities.About the RoleThis is a freelance...

About the PositionIQVIA is seeking a highly skilled Clinical Research Associate to join their team. The successful candidate will be responsible for ensuring that sites are conducting studies and reporting data as required by the study protocol, applicable regulations, and sponsor requirements.Key ResponsibilitiesConduct site selection, initiation,...

Clinical Research Manager plays a pivotal role in the successful delivery of clinical studies within Global Medicines Development (GMD). Key responsibilities include overseeing study protocol development, set-up, maintenance, close-out, and archiving. Effective collaboration with internal and external partners is crucial to ensure timely, cost-effective, and...

About AbbVieAt AbbVie, our mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services...

Innovaderm Research seeks an experienced Site Budget and Contract Lead to join our team. As a key member of our operations department, you will play a crucial role in the development of investigator budget and contract proposals.This position requires strong analytical and problem-solving skills to effectively manage multiple projects simultaneously. You...

IQVIA Clinical Research Associate PositionWe are currently looking for a skilled Clinical Research Associate to join our IQVIA Argentina team.The chosen candidate will be responsible for performing site management tasks, including conducting monitoring and initiation visits, and ensuring that all required documentation is maintained accurately.Key...

QualificationsTo be considered for this role, you must have a Bachelor's Degree in a scientific discipline or healthcare, prior clinical trial experience, including experience in a management/leadership capacity or an equivalent combination of education, training, and experience.You should also have effective time management skills and the ability to manage...

Our MissionWe're committed to transforming the world for patients everywhere. Our employees come together to tackle new challenges and advance healthcare.Parexel's 360° Patient-First Portfolio ensures that the patient is represented at every step of the clinical trial process.22,000+ employees worldwide.40+ years of experience in clinical research.1,167...

Parexel International is a leading clinical research organization (CRO) dedicated to advancing healthcare through innovative and patient-centric solutions. As a Biostatistician at Parexel, you will play a crucial role in shaping the future of medicine by analyzing data and developing statistical models to inform clinical trials.We are seeking highly skilled...

At ICON plc, we're seeking a highly skilled Pharmacovigilance Assistant to join our team in Warsaw.This role is part of our diverse and dynamic team responsible for the collection, documentation, and reporting of safety data related to medications and clinical trials.The successful candidate will play a key role in ensuring compliance with regulatory...

Rho, Inc. is seeking a skilled Clinical Research Project Coordinator Freelancer to join our team as a freelance professional.Job SummaryThe Clinical Research Project Coordinator Freelancer will be responsible for supporting the preparation of Investigator Site Files (ISFs), maintaining the Trial Master File (TMF), and uploading country and site level...

Responsibilities:As a Research Project Coordinator, you will play a vital role in supporting the Global Study Associate Director in managing clinical studies. Key responsibilities include providing oversight to ensure study delivery, preparing delegated study documents, and maintaining interactions with internal and external functions.The ideal candidate...

Job SummaryWe are seeking a talented Clinical Research Associate to perform site management work, ensuring compliance with study protocols, regulations, and sponsor requirements.ResponsibilitiesPerform site visits, document findings, and maintain accurate records.Support recruitment efforts, track regulatory submissions, and manage case report forms.Evaluate...