Trial Master File Coordinator

Key ResponsibilitiesA Clinical Trial Assistant will be responsible for providing administrative support to the Clinical Research Associates and Regulatory and Start-Up teams. Key responsibilities include:Updating and maintaining clinical documents and systems.Preparing, handling, distributing, filing, and archiving clinical documentation and...

Job DescriptionThe Trial Operations Coordinator role at IQVIA Argentina involves working closely with cross-functional teams to deliver clinical studies. The successful candidate will have experience in project coordination and a strong understanding of clinical trial conduct.Responsibilities:Achieve project quality by identifying quality risks and issues,...

Xepelin is a pioneering force in global healthcare, pushing the boundaries of clinical research to transform lives. We're excited to announce the recruitment of a talented Global Clinical Trial Coordinator to join our team! As a coordinator, you'll play a pivotal role in supporting the management of clinical investigators and sites, ensuring smooth trial...

Role SummaryThe Regulatory Coordinator is responsible for coordinating clinical trial submissions and ensuring compliance with regulatory requirements. This involves working closely with the internal study team, sponsor, and external stakeholders to ensure timely and accurate submissions.Main ResponsibilitiesCoordinate clinical trial submissions and track...

Job OverviewPerform 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...

ResponsibilitiesPrepare investigator sites to conduct clinical trials through review and approval of essential clinical trial and regulatory documents.Establish site activation timelines with selected sites and coordinate activities to meet planned activation timelines.Communicate with clinical sites during site start-up and collaborate with other functional...

Job OverviewPerform 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...

The Project Coordinator works with Project Managers, Clinical Trial Managers, Site Selection Team and Clinical Research Associates (CRA) to provide administrative and coordinating support for site activation activities and other site level deliverables through all phases of the clinical trial lifecycle.As a Project Coordinator, you will take the lead to...

Job OverviewA Clinical Trial Assistant provides administrative support to the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery. Key responsibilities include:Assisting CRAs and RSU team with updating and maintaining clinical documents and systems.Preparing, handling, distributing,...

About the RoleThis exciting opportunity is for a Clinical Trial Coordinator - Regulatory Expertise to join our dynamic team. The successful candidate will work closely with cross-functional teams to ensure regulatory compliance and contribute to the development of innovative biopharmaceutical solutions.ResponsibilitiesAssist in the identification and...

Job OverviewAs a key member of the clinical research team, the successful candidate will perform daily administrative tasks to ensure the timely and accurate delivery of Trial Master Files. This role requires close collaboration with Clinical Research Associates and Regulatory and Start-Up teams to maintain accurate records and track site compliance.Key...

Job DescriptionThe Administrative Coordinator - Community Management will play a crucial role in supporting the Community Manager in ensuring the smooth operation of the HOA. This includes communicating directly with homeowners and board members, maintaining records, and handling administrative tasks.ResponsibilitiesManage HOA owner and board member...

VML South Africa is seeking a skilled Marketing Analytics Coordinator to join our team.About the Role:In this role, you will be responsible for coordinating marketing analytics efforts. You will work closely with our global enablement leads and local teams to drive the success of our partnerships.Key Responsibilities:You will develop monthly and ad hoc...

At IBM Computing, our goal is to deliver exceptional results through project management expertise.As a Business Project Coordinator, you will be responsible for creating and maintaining client relationships, meeting financial targets, and driving opportunities for business growth.Key responsibilities include:Managing client expectations and...

Customer Acquisition Coordinator Job DescriptionThis role involves researching target companies, identifying key prospects, and gathering accurate contact information for potential business opportunities.ResponsibilitiesAnalyze provided company lists to identify the most promising 3-5 prospects per company based on established criteria.Research target...

IQVIA Biotech is hiring in Argentina Join our team as a Clinical Research Associate.The ideal candidate will have varied therapeutic experience and be willing to work across multiple therapeutics including: Oncology, Cardiovascular, Internal Medicine, & Ophthalmology.This role will be home-based in Buenos Aires, Argentina.Job Description Summary Perform...

Role Description: As a Clinical Research Associate II at AbbVie, you will be part of a dynamic team driving innovation in clinical research. Your key responsibilities will include:Key Tasks:Collaborate with study teams to develop and execute clinical trial strategies.Provide guidance and support to site staff and principal investigators on trial execution...

Job Description:The Adverse Event Intake Coordinator plays a pivotal role in ensuring the timely and accurate processing of adverse event reports related to our company's products. This position is responsible for receiving, reviewing, and processing incoming adverse event reports from various sources, including healthcare professionals, consumers, and...

About the Role:We are seeking an experienced Clinical Research Manager to join our team at Msd. The successful candidate will be responsible for the end-to-end performance of assigned protocols in a country, ensuring compliance with regulations, company policies and procedures, quality standards, and adverse event reporting requirements.The ideal candidate...

Job Title: Administrative Coordinator - Community Management Location: Remote (MST Time Zone) Salary Range: up to 1800 USD Work Schedule: Monday - Friday, 8:00 AM to 5:00 PM (MST) Additional Availability:Occasionally required for HOA board meetings Monday Thursday | 4:00 PM 8:00 PM (MST), held via Zoom NOTE: INDEPENDENT CONTRACTOR POSITION Company Overview:...