Clinical Trials Assistant 1

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...

Job Overview The Clinical Trial Educator (CTE) will provide information and education on clinical trial inclusion and exclusion criteria to trial coordinators and healthcare providers. Also provides in-service presentations with the goal to increase patient enrollment. Works in partnership with CRAs and other field-based medical teams for optimal trial...

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 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...

Job Overview:The Clinical Trials Assistant is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the Clinical Trials Assistant shall reflect their experience, and level of contribution which they can make to the project.Key Responsibilities:Document and track...

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...

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 Summary: Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We...

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...

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...

Unlock a Career in Clinical ResearchWe are seeking a skilled and dedicated Clinical Trial Coordinator to join our team at Thermo Fisher Scientific. As a Clinical Trial Coordinator, you will play a crucial role in the success of our clinical trials, working closely with our clients to ensure timely and efficient project delivery.About the RoleThis is a...

About the JobWe are seeking a highly skilled Clinical Trial Assistant to join our team at ICON. As a Clinical Trial Assistant, you will play a key role in the management and coordination of clinical trials.Responsibilities:Recruitment and Site Management: Perform site feasibility assessments, negotiate agreements, and ensure accurate tracking and...

CTM II 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. At ICON, it's our people that set us apart. Our diverse teams enable us to become a...

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...