filing

IQVIA is seeking an administrative support specialist to assist with Trial Master File delivery and regulatory/start-up activities. You will collaborate with CRAs and RSU to update, file and archive clinical documents, ensuring site compliance and alignment with project timelines.Your role includes handling documentation, coordinating with clinical teams,...

About World Business Lenders (www.wbl.com) World Business Lenders (WBL) is proud to offer short-term, real estate-backed commercial loans to a diverse range of small and medium-sized businesses across the United States, especially those who may find it challenging to secure traditional financing. Typically, the work schedule is from 9:00am to 6:00pm Eastern...

Overview Who We Are Because health is personal. That's why Personify Health created the first and only personalized health platform—bringing health plan administration, holistic wellbeing solutions, and comprehensive care navigation together in one place. We serve employers, health plans, and health systems with data-driven solutions that reduce costs...

ResponsibilitiesReview hospital files under supervision of the principal investigator to assist preliminary volunteer screening during the recruitment period, ensure all necessary permits are obtained, and help find eligible volunteers.Assist study personnel assigned to the trial in screening volunteers deemed eligible for the trial protocol by the principal...

The Site Coordinator is responsible for the effective management and conduct of clinical trials under the supervision of the Principal Investigator. This role includes planning daily activities, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The Site Coordinator facilitates communication between the...

We are seeking trustworthy "Accountants" who work efficiently without sacrificing accuracy for a leading manufacturing regional group. Accountant Duties and Responsibilities: Properly control and classify TB accountsIssue and register e-invoices in the portal, Lean reconciliation and bank transactions journal entriesPrepare local treasury operations...

The Site Coordinator is responsible for the effective management and conduct of clinical trials under the supervision of the Principal Investigator. This role includes planning daily activities, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The Site Coordinator facilitates communication between the...

The Site Coordinator is responsible for the effective management and conduct of clinical trials under the supervision of the Principal Investigator. This role includes planning daily activities, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The Site Coordinator facilitates communication between the...

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 FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

The Site Coordinator is responsible for the effective management and conduct of clinical trials under the supervision of the Principal Investigator. This role includes planning daily activities, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The Site Coordinator facilitates communication between the...

Description we are seeking for Seafreight Export LCL Operation Executive to join our team in our EGS/Istanbul Dunya Ticaret Merkezi - Bakırköy Istanbul office. Department Department: Export Location Location: Istanbul Key Responsibilities To work with all suppliers, agents and related department in order to meet with customer demands in compliance with...

The Site Coordinator is responsible for the effective management and conduct of clinical trials under the supervision of the Principal Investigator. This role includes planning daily activities, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The Site Coordinator facilitates communication between the...

We are recruiting for a Quality Control Operator to join our team and play a key role in ensuring the highest standards of quality, accuracy and print readiness across packaging artwork files. The ideal candidate will have around 5 years of experience in artwork, prepress, print production or quality control, with a strong understanding of the packaging...

OverviewThe Site Coordinator is responsible for the effective management and conduct of clinical trials under the supervision of the Principal Investigator. This role includes planning daily activities, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The Site Coordinator facilitates communication between...

The Site Coordinator is responsible for the effective management and conduct of clinical trials under the supervision of the Principal Investigator. This role includes planning daily activities, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The Site Coordinator facilitates communication between the...

The Site Coordinator is responsible for the effective management and conduct of clinical trials under the supervision of the Principal Investigator. This role includes planning daily activities, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The Site Coordinator facilitates communication between the...

The Site Coordinator is responsible for the effective management and conduct of clinical trials under the supervision of the Principal Investigator. This role includes planning daily activities, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The Site Coordinator facilitates communication between the...

The Site Coordinator is responsible for the effective management and conduct of clinical trials under the supervision of the Principal Investigator. This role includes planning daily activities, ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). The Site Coordinator facilitates communication between the...

A leading global spirits company is seeking an Office and Human Resources Coordinator in Turkey. This hybrid role involves supporting HR operations, managing employee files, and enhancing engagement initiatives. Ideal candidates should possess advanced proficiency in English and experience in office or HR administration. Strong organizational and...

Michael Page is seeking a detail-oriented Accounting Specialist to join a reputable retailer. You will contribute to the Accounting & Finance department by ensuring financial accuracy and compliance across records and reports.The role emphasizes collaboration with auditors, support for budgeting and forecasting, and involvement in tax filings, with English...