Associate Project Coordinator, Study Operations

The Associate Project Manager ensures the successful initiation, planning, execution, monitoring, controlling and closure of assigned clinical research projects. The Associate Project Manager must ensure compliance with the study budget, project scope and timelines and in accordance with applicable standard operating procedures (SOPs), good clinical...

Role & Responsibilities - Development of Sponsor Project Plans (SPPs). - Establish project start-up timelines (including milestones, tasks lists, and dependencies) and track start - up progress through internal meetings and trackers. - Coordinate the development and communication of technical requirements to facilitate receipt of data transfers from...

**Associate Study Start-Up Manager** **IQVIA Biotech** Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. **Essential Functions**: - Oversee the execution of Site...

ICON has an exciting new opportunity for a Global Project Manager to join a growing and successful team. This is a home-based and permanent role. Key Responsibilities: Responsible for: - Lead the development of realistic study timelines, from design through final study reporting Maintaining accuracy of clinical study timeline information in data control...

Job Overview Associate Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with...

Spain, Remote **Job ID** R0000014735 **Category** Clinical Trials **ABOUT THIS ROLE**: **Position Purpose**: - The Senior Study Manager (SSM) has responsibility for one or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studies - The SSM leads and manages the tactical execution of one or more...

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator. This part-time (24 hours) role, is planned for 11 months and is to support the site in **Majadahonda** in conducting a clinical trial in the field of...

Job Purpose: As our project coordinator, you become a member of a project team, supporting day-to-day project activities related to the localization process. Tasks will include client data management, project set up, scheduling, project file organization, and placing tasks with linguists. Your primary responsibility will be to coordinate the completion of...

IQVIA is looking for a motivated and detail-oriented Associate Project Manager to manage the translation development projects of Clinical Outcomes Assessments (COAs). **Job **Summary** **Responsibilities** - Assist in the planning, coordination, and execution of translation and linguistic validation projects, with adherence to project scope, timeline, and...

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator. This fill-time (40 hours) role, is planned for 11 months and is to support the site in **Barcelona** in conducting a clinical trial in the field of **Cardiology**. As...

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator. This part-time (20 hours) role, is planned for 11 months and is to support the site in** El Palmar, Murcia** in conducting a clinical trial in the field of...

These customers have new therapeutic ideas, but want a partner who can assist with the clinical trial process, the complexities of certain disease states, or other critical capacities. You’ll work with them on the newest treatment breakthroughs for some of the most perplexing conditions. And ultimately, you’ll help make a positive difference in...

We are looking for Project Leader/ Senior Project Leader’s to join our innovative and dynamic group of global professionals dedicated to assisting our clients in driving healthcare forward. This is an important and high-profile role within our Research & Development Operation business unit to enable medical breakthroughs that advance healthcare and patient...

**Overview** At the heart of QIAGEN’s business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the...

Senior Projects Managers are crucial to the success of Clinical Trials managed by Innovaderm. They are the main point of contact internally as well as externally, ensuring all activities and deliverables are completed on time, on budget, and as expected. Great project managers go further than creating project plans and following up on tasks. They show...

**About Qualifyze** Founded in September 2017, Qualifyze is the fastest growing 3rd party audit provider in the world. Our success builds on a one-of-a-kind digital audit platform that connects the most important stakeholders of the pharmaceutical industry: manufacturers, suppliers, and auditors. With Qualifyze, customers can solve their audit demand 100%...

The Associate Director, Patient Recruitment defines recruitment & retention strategies and tactics, which are site and patient centric, as well as explores and implement innovative patient recruitment and site engagement strategies in close collaboration with both internal and external stakeholders and specialized patient recruitment vendors (when...

The **Initiation Clinical Research Associate II **(**iCRA II**) specialises in performing all study start up activities for a clinical trial. You will participate in Pre SIV activities and be assigned & accountable for managing and driving the strategy for the Pre SIV / start up tasks of the study. The iCRA II can also support protocol amendments if...

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...

As a Clinical Project Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **We are looking for experienced Project Managers with substantial experience in multi-country/global PM experience.** **What you will be doing**: - The Study Manager has responsibility 1 or more...