Site Activation Partner I

Spain, Remote **Job ID** R0000015394 **Category** Clinical Trials **ABOUT THIS ROLE**: The FSP division of Parexel FSP is seeking a Site Activation Partner based in Spain. **Position Purpose**: - The Site Activation Partner is responsible for leading or supporting operational activities from start-up to close-out, for assigned studies and investigator...

Spain, Remote **Job ID** R0000015136 **Category** Clinical Trials **ABOUT THIS ROLE**: Additional Job Description In Parexel FSP we are looking for a Site Activation Partner based in Spain. **Position Purpose**: - The Site Activation Partner is responsible for leading or supporting operational activities from start-up to close-out, for assigned studies...

Job Overview Under general supervision, perform tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include feasibility or maintenance activities. Essential...

As a S **ite engagement Liason **you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: **Accountable for site start-up and activation** - Deploy GSSO site strategies by qualifying and activating assigned sites - Supports processes to optimize country &...

As a Site Engagement Liaison you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - Responsible for site and monitoring quality, regulatory and GCP compliance. - Drive inspection readiness and provide support for site audits/inspections as needed,...

The Study Operations Manager II is responsible for study and regional/country level activities from study startup through conduct and study close. The Study Operations Manager will be assigned one or more studies and will be tasked with taking on several responsibilities in support of the larger Study Management deliverables. The Study Operations Manager II...

**Job Summary**: Site Manager - Outage is responsible for preparation, planning, leading execution, and close out of complex project/outages events for gas turbine, steam turbine and generator power plants while supporting the development of the business strategy for field fulfilment excellence in FieldCore. The Site Manager - Outage is a focal role, with...

**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...

The Director, Start-Up is responsible for providing leadership and oversight to site contracting, and site activation teams, ensuring alignment with study and site activation timelines. The Director, Start-Up will provide leadership to functional leads of Site Selection and Site Contracting. The Director, Start Up has line management responsibility for...

**Job Overview** 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. **Fluent in Spanish and English.** **Essential Functions** - Oversee the execution of Site Activation...

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. As a Clinical Research Associate you will be joining the world’s largest & most comprehensive...

As a Contract Analyst you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The Contract Analyst works with crossfunctional team members on development of the study CTA/budget templates and escalation of language or costs that cannot be agreed to in the negotiation process. The...

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...

As a CRA you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently or as part of the client and ICON team. You will be managing competing priorities, supporting...

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. As a Clinical Research Associate you will be joining the world’s largest & most comprehensive...

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...

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...

As a Clinical Project Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - The Study Operations Manager is responsible for study and regional/country level activities from study startup through conduct and study close. The Study Operations...

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...

**Main Function** We are looking for an Adoption Lead role who will be an integral part of the myBuy program. The Adoption Lead will be responsible to ensure that all OCM aspects of the myBuy deployment are taken into consideration, understood and followed. The Adoption Lead will be looking after a core site or RSS cluster and will ensure that the OCM...