Clinical Research Operations Specialist

Job Title: Clinical Trial Associate II, TMF Operations SpecialistJob Summary:We are seeking a highly organized and detail-oriented Clinical Trial Associate II, TMF Operations Specialist to join our team at Worldwide Clinical Trials. In this role, you will be responsible for processing, maintaining, and archiving all essential documents in compliance with...

We are seeking a highly skilled Clinical Research Coordinator to join our team at Clinical Trial Network in Houston, Texas.This full-time position offers an exciting opportunity for a motivated individual to work in clinical research and contribute to the planning, implementation, and coordination of studies.Responsibilities:Coordinate and manage all aspects...

Fortrea, a leading global contract research organization (CRO), is seeking a highly skilled Global Clinical Research Operations Manager to join our team. As a passionate advocate for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical...

Job Overview:The Clinical Research Associate - Site Monitoring Specialist is responsible for ensuring the integrity and quality of clinical trial data. This role involves monitoring investigator sites, conducting on-site file reviews, and maintaining effective communication with investigative sites, client companies, and project teams.

**Job Summary**The Regulatory Intelligence Department at Syneos Health plays a crucial role in shaping decision-making at the highest levels. The team analyzes and refines Syneos Health regulatory intelligence from internal and external sources, combining knowledge from therapy areas and functions to deliver proactive advice outlining risks and new...

About the RoleWe are seeking a skilled and detail-oriented Global Clinical Trials Operations Coordinator to join our team at Worldwide Clinical Trials. In this role, you will play a critical part in ensuring the smooth operation of our clinical trials.

Parexel Clinical Study Team Assistant II Job Description">About Parexel: We are a global leader in clinical research outsourcing. Our mission is to help pharmaceutical, biotech, and medical device companies accelerate their product development.Job Title: Clinical Study Team Assistant IILocation: Remote, MexicoAbout the Role:">We are seeking a highly...

At Icon Plc, we're driven by a passion to advance and improve patients' lives. Our diverse teams enable us to become a better partner to our customers, and we're committed to delivering excellence at every touch-point.We foster an inclusive environment where everyone feels valued and empowered to make a meaningful impact. As a Clinical Research Coordinator -...

Job OverviewWe are seeking a highly organized and detail-oriented Clinical Trial Operations Specialist to join our team at Iqvia. This is an exciting opportunity for someone with a passion for clinical research and excellent communication skills.About the RoleIn this role, you will be responsible for performing site activation activities in assigned studies,...

OverviewICON plc is a world-leading healthcare intelligence and clinical research organization, dedicated to advancing clinical research and providing outsourced services to pharmaceutical, biotechnology, medical device, and government organizations.SalaryWe offer a competitive salary ranging from $80,000 to $110,000 annually, depending on experience and...

Clinical Research Associate RoleAt Thermo Fisher Scientific, we are seeking a skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for performing and coordinating all aspects of the clinical monitoring and site management process.Key Responsibilities:• Monitor investigator sites with a risk-based...

Job OverviewAs a Clinical Trial Assistant at Iqvia, you will play a crucial role in ensuring a complete and accurate Trial Master File delivery. This involves working closely with the Clinical Research Associates and Regulatory and Start-Up teams to perform daily administrative activities.Key Responsibilities:- Assist Clinical Research Associates and...

Job DescriptionWe are seeking a skilled Clinical Research Site Lead to join our team at MSD. As a key member of our operations team, you will be responsible for ensuring compliance with Good Clinical Practice (GCP) guidelines and regulations in clinical research studies.Key Responsibilities:Manage and monitor clinical research sites to ensure adherence to...

About the RoleWe are seeking a skilled Clinical Trial Coordination Specialist to join our team at Thermo Fisher Scientific. As a key member of our clinical trial operations, you will play a crucial role in ensuring the successful execution of clinical trials.

At ICON plc, we are committed to advancing and improving patients' lives. Our diverse teams enable us to become a better partner to our customers and help us fulfill this mission.We are a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced services to...

Lead Clinical Operations for ICON PlcICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.Our teams are at the core of our culture and the...

**About ICON**We are the world's largest and most comprehensive clinical research organisation, driven by healthcare intelligence. Our mission is to improve human health outcomes through our expertise in clinical research.**Competitive Salary and Benefits**We offer a competitive salary of $60,000 - $80,000 per annum, depending on location and experience. In...

Job OverviewWe are seeking a highly skilled Clinical Operations Manager to join our team at MSD. In this role, you will be responsible for the execution and oversight of clinical trial country submissions and approvals.About the RoleThe ideal candidate will have 5 years of experience in clinical research or a combination of clinical research and related...

Parexel is a leading Clinical Research Organization (CRO) company that specializes in delivering life-changing medicines to patients.We are seeking a skilled Clinical Operations Assistant to join our Latin American team. This is an exciting opportunity for someone who wants to make a difference in the lives of patients.The role of the Clinical Operations...

Job TitleClinical Document SpecialistAbout the RoleWe are seeking a highly organized and detail-oriented Clinical Document Specialist to join our global Clinical Pharmacology Services team. As a Clinical Document Specialist, you will be responsible for maintaining and organizing clinical documents related to our projects, ensuring that all documentation is...