Clinical Trial Educator

**Job Overview**The Clinical Trial Educator, based in our global network, will collaborate with trial coordinators and healthcare providers to provide information and education on clinical trial inclusion and exclusion criteria.This role requires working in partnership with CRAs and other field-based medical teams to develop tailored recruitment plans and...

Principal Clinical Research AssociateJob SummaryCTI Clinical Trial Services, Inc. is seeking a highly skilled and experienced Principal Clinical Research Associate to join our team. As a key member of our clinical operations team, you will be responsible for overseeing the management of clinical trials, ensuring compliance with regulatory requirements, and...

Job SummaryClinical Trial Services, Inc. is seeking a highly skilled Clinical Research Associate Lead to join our team. As a Clinical Research Associate Lead, you will be responsible for overseeing the conduct of clinical trials at assigned sites, ensuring compliance with regulatory requirements, and providing guidance to site staff.Key...

Clinical Research Excellence at CTI Clinical Trial Services, IncWe maintain a culture of excellence across all regions by ensuring our remote employees are fully engaged. To achieve this, we hold weekly all-staff meetings. Each department provides an update on their study or milestone progress. Additionally, our employees can participate in one of our CTI...

Medpace, Inc. is seeking a full-time Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo. This position plays a key role in the clinical trial management process.Key Responsibilities:Efficiently manage and successfully execute clinical trial submissions.Collaborate with cross-functional teams to ensure timely and accurate...

**About ICON Plc**We are a world-leading healthcare intelligence and clinical research organization.Our mission is to shape the future of clinical development, and we welcome you to be a part of it.We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team.As a Clinical Trial Administrator at ICON, you will play a pivotal...

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Key Responsibilities:As a Regulatory Submissions Manager at Medpace, you will play a vital role in the clinical trial management process. Your primary focus will be on efficiently managing and successfully completing regulatory submissions for our LATAM clinical trials.Key Skills and Qualifications:• Strong expertise in clinical trial management and...

**Clinical Trials Manager Role**At Amgen, we're committed to serving patients through innovative treatments. As a Clinical Trials Manager, you'll play a vital role in leading and coordinating clinical trials from start to finish.**Key Responsibilities:**- Partner with global and local teams to drive study progress and delivery- Plan, manage, and oversee...

Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As a Clinical Trials Analyst II at Thermo Fisher Scientific, you will have the opportunity to lead and support our clients in the execution of clinical trials logistics. Key responsibilities include supporting both foreign and domestic clients in the planning and execution of...

Company OverviewICON plc is a global healthcare intelligence and clinical research organization dedicated to fostering innovation and excellence. Our diverse and dynamic team is committed to shaping the future of clinical development.SalaryWe offer a competitive salary of $65,000 - $85,000 per annum, commensurate with experience, in addition to a range of...

Job DescriptionWe are seeking an experienced Global Clinical Trials Manager to join our team at Allucent. As a key member of our clinical operations department, you will be responsible for providing leadership and management to the Clinical Research Associates (CRAs) and other clinical functional groups in their day-to-day clinical trial activities.Your...

Clinical Trial Manager - Argentina, Buenos Aires 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. We are currently seeking a Clinical Trial...

Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest...

**Principal Clinical Research Associate** **Please submit your CV in English for Quickest Review Process!** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or...

Job SummaryWe are seeking a highly skilled and experienced Clinical Trials Manager to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for providing leadership and management to our Clinical Research Associates (CRAs) and other functional groups in their day-to-day clinical trial activities.Key...

Job Advert Posting ICON 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. With our patients at the centre of all that we do, we help to...

Diversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest...

Medpace, Inc. is seeking a full-time Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo. This position plays a key role in the clinical trial management process. Key responsibilities include efficiently managing and successfully submitting regulatory documents.Key Responsibilities:Manage and submit regulatory documentsCollaborate...