The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle. The CP&P team interacts with discovery and translational scientists, project leadership, early and la...
Budgeting, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems (CTMS), Clinical Trials, Clinical Trials Monitoring, Communication, Data Analysis, Decision Making, Financial Analysis, Health Sciences, Life Science. Excellent knowledge of the drug development process specifica...
Key Responsibilities:Lead business development and capture for opportunities within federal agenciesDirect and manage large clinical trials support services contracts or projectsMentor a team of clinical research professionals and foster a culture of continuous improvementRequired Qualifications:Mas...
Budgeting, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems (CTMS), Clinical Trials, Clinical Trials Monitoring, Communication, Data Analysis, Decision Making, Financial Analysis, Health Sciences, Life Science. We have an opportunity for a Senior Clinical Research Associa...
The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle. The CP&P team interacts with discovery and translational scientists, project leadership, earl...
Accountable for all country clinical/medical aspects associated with Development and prioritized Re-search programs/trials by providing clinical strategic and tactical leadership as the Country Clinical Development representative. Provides robust indication, compound, and protocol training: To the c...
Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a minimum of 3 years’ experience in monitoring pharmaceutical industry clinical trials. Have an in-depth knowledge of Good Clinical Practice, ICH g...
The Clinical Research Associate (CRA) is responsible for the implementation, monitoring, and summarization of clinical trials in compliance with protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations, and Standard Operating Procedures (SOPs) to ensure patient safety. Senior Cli...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. If applicable, may be accountable for site financial management ac...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Perform site monitoring visits (selection, initiation, monitori...
As a Sr CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Primary interfaces: Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials. Have a mini...
Senior Clinical Research Associate. Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
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 as a Clinical Research Associate II assigned to Early Development trials (Phase I). ICON plc is a world-leading healthcare intell...
IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring experience in one of the following therapeutic areas: Central Nervous System (CNS) or Cardiovascular/Renal/Metabolic (CVRM). IQVIA is a leading global provider of advanced analytics, technology solutions and cl...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
The Clinical Research Associate (CRA) is responsible for the implementation, monitoring, and summarization of clinical trials in compliance with protocols, Good Clinical Practice (GCP), ICH Guidelines, federal regulations, and Standard Operating Procedures (SOPs) to ensure patient safety. A0;is seek...
As a Clinical Research Associate at Parexel, you will be joining a team with a wide variety of experiences and knowledge. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical ...
Your efforts will contribute to the safety and well-being of patients while adhering to the highest standards in clinical research. Be a part of groundbreaking research that can improve patient lives. Develop strong relationships with clinical investigative sites and a supportive team. Developing an...