Global Clinical Trials Coordinator

About the CompanyMaxis Clinical Sciences is a leading provider of complete solutions for clinical and digital services. With a global presence across three continents, we offer 24/7 delivery and operate with a problem-solving approach that prioritizes genuine relationships and steady communication.About the RoleThe Senior Clinical Trial Manager will join our...

About the RoleAs a Senior Labeling Specialist at TalentBurst, you will play a key role in ensuring timely and accurate labeling of medical products for global clinical trials. This is an exciting opportunity to leverage your expertise in clinical trial regulations, packaging, and labeling to drive business growth.

Supply Chain Project Manager Job DescriptionWe are seeking an experienced Clinical Trial Supply Chain Project Manager to join our team in Ridgefield, Connecticut.About the PositionThe successful candidate will have a strong background in project management, regulatory compliance, and supply chain operations. They will be responsible for representing the...

Job Title: Clinical Trials Labeling SpecialistAbout Nesco ResourceNesco Resource is a leading provider of clinical trial solutions, dedicated to delivering high-quality services to our clients.Estimated Salary: $70,000 - $90,000 per yearJob DescriptionAbout the Role:We are seeking an experienced Clinical Trials Labeling Specialist to join our team. In this...

Job SummaryWe are seeking an experienced Clinical Trials Site Monitoring Lead with a strong background in Oncology, Metabolic, CNS, and Dermatology to join our team at Yoh. In this role, you will be responsible for leading the execution of monitoring plans and overseeing the quality of monitoring performed by CRAs for assigned US conducted trials.About the...

**About the Role**We are seeking a highly skilled Clinical Research Associate to join our team at McInnis Inc. As a key member of our clinical research operations, you will play a critical role in supporting the execution of clinical trials.**Key Responsibilities:**Act as the primary point of contact with assigned clinical study sites during start-up...

Job OverviewMcInnis Inc. is a leading organization in the clinical trials industry, and we are currently seeking an experienced Clinical Trial Operations Manager to join our team.

Key ResponsibilitiesThe Administrative Assistant - Clinical Trials will provide administrative support to our Business Operations Team, focusing on data entry, record-keeping, and document management.This role requires a high level of accuracy, attention to detail, and organizational skills, as well as the ability to maintain confidentiality and handle...

About the RoleWe are seeking a highly skilled Clinical Trials Operations Specialist to join our team at McInnis Inc. in Ridgefield, CT. As a member of our Trial Master File (TMF) team, you will play a critical role in ensuring the smooth operation of our clinical trials.

About McInnis Inc.We are seeking a highly motivated individual to join our team as a Clinical Trial Document Specialist. As a hybrid position, this role will involve working from home and commuting to our Ridgefield, CT location on a weekly basis.

Company Overview:Yoh, a Day & Zimmermann company, is a leading global staffing company with over 65 years of experience in the US, UK, and Canada. We specialize in connecting professionals like you with exciting career opportunities across multiple industries.Job Summary:We are seeking an experienced Clinical Trial Supply Chain Project Manager to join our...

Job OverviewMcInnis Inc. is seeking a highly skilled Clinical Data Entry Coordinator to support our Business Operations Team.This full-time role involves entering accurate information in various applications, including the Investigator Database, Clinical Trial Management System (CTMS), and AGS360 or equivalent aggregate spend system.

Job OverviewThis Senior Clinical Trial Manager role offers a unique opportunity to join a leading company in the clinical research industry. As a key member of our team, you will be responsible for overseeing the execution of monitoring plans and ensuring the quality of monitoring performed by CRAs for assigned US conducted trials.Key ResponsibilitiesDevelop...

Job DescriptionThe Label Development Specialist is accountable for the efficient management of labeling activities, including planning, monitoring, and steering timelines, tasks, and costs. This role ensures timely provision of IMP labels for assigned trials by communicating and negotiating all labeling-related activities within the Global Trial Team.Review...

About the JobWe are looking for a highly organized and proactive individual to join our team as an Administrative Assistant in Ridgefield, CT. The ideal candidate will have a strong background in travel and expense management and be proficient in MS Office.Job DescriptionThe successful candidate will manage and process travel arrangements and expense reports...

Job DescriptionWe are seeking a highly skilled Senior Label Development Specialist to join our team at Nesco Resource.About the RoleThis is a key position in our organization, responsible for processing, planning, and steering timelines, tasks, and costs for labeling activities performed at internal or external vendors supporting global clinical trials phase...

About the RoleWe are currently seeking a skilled professional to join our team as an Administrative Assistant in Ridgefield, CT. This role offers a unique opportunity to support our team's travel and expense management needs.Key ResponsibilitiesManage and process travel arrangements and expense reports for team members with accuracy and timeliness.Utilize...

Job DescriptionIn this Data Management and Operations Coordinator role, you will be responsible for creating, maintaining, and updating investigator and site data in CTMS based on Regulatory documents and/or from pre-designed templates.You will also update CTMS trial information related to investigators in the BIPI Investigator Database, create, update, and...

About the RoleThe Data Management Coordinator will be responsible for managing and maintaining high-quality data across various systems, ensuring accuracy and compliance with regulatory requirements.This role requires exceptional organizational and communication skills, as well as the ability to work effectively in a team environment and adapt to changing...

Job Title: Statistical ProgrammerJob Summary:We are seeking a skilled Statistical Programmer to join our team at PSG Global Solutions Careers. As a Statistical Programmer, you will be responsible for developing and maintaining datasets, extracting data from various databases, and developing programs to analyze data and produce reports.Key...