Sr Site Activation Coordinator

hace 8 meses


En remoto, España IQVIA A tiempo completo

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 Functions
- Under general supervision, perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.
- Prepare site documents, reviewing for completeness and accuracy.
- Inform team members of completion of regulatory contractual. and other documents for individual sites.
- Distribute completed documents to sites and internal project team members.
- Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.
- Review, track and follow up the progress, the approval and execution of required documents such as questionaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.

**Qualifications**:

- Bachelor's Degree Life science or related field Req



  • En remoto, España Parexel A tiempo completo

    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...


  • En remoto, España Parexel A tiempo completo

    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...


  • En remoto, España Parexel A tiempo completo

    Spain, Remote **Job ID** R0000017249 **Category** Clinical Trials **ABOUT THIS ROLE**: 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 and investigator sites to...


  • En remoto, España ICON A tiempo completo

    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 &...


  • En remoto, España Pfizer A tiempo completo

    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...


  • En remoto, España IQVIA A tiempo completo

    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...


  • En remoto, España IQVIA A tiempo completo

    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...


  • En remoto, España IQVIA A tiempo completo

    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...


  • En remoto, España IQVIA A tiempo completo

    **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...

  • Director, Start-up

    hace 6 meses


    En remoto, España Innovaderm Research A tiempo completo

    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...


  • En remoto, España IQVIA A tiempo completo

    **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...


  • En remoto, España IQVIA A tiempo completo

    **Overview** To meet our client expectations and retain the excellent reputation built up over time the IQVIA PCS team is committed to recruiting, training and supporting driven individuals who have both consulting skills and life science skills that can be applied to PCS research activities. Individuals joining us are assured of a rewarding and progressive...

  • Contract Analyst

    hace 6 meses


    En remoto, España ICON A tiempo completo

    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...


  • En remoto, España Innovaderm Research A tiempo completo

    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...


  • En remoto, España IQVIA A tiempo completo

    **PURPOSE** To provide project related support and assistance across multiple projects, sites and teams and Review the structured clinical data output with access to medical charts. To ensure the work is conducted as per SOPs, Policies and Good clinical practice’s and applicable regulatory requirements. Adherence to protocol, overall completeness, and...

  • Sr Site Budget

    hace 6 meses


    En remoto, España IQVIA A tiempo completo

    **Job Overview** Oversees, supervises and manages the operational aspects of ongoing projects and programs ensuring quality deliverables on time and within budget. Will ensure that all project work is completed in accordance with SOPs, policies and practices. Manage staff in accordance with organization’s policies and applicable regulations. **Essential...


  • En remoto, España Parexel A tiempo completo

    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...


  • En remoto, España Semrush A tiempo completo

    Hi there! We are Semrush, a global IT company developing our own product - a platform for digital marketers. New stars are born here, so don’t miss your chance. This is our role Freelance Project Coordinator for idea generators, planning geniuses, and natural-born marketers. **Tasks in the role**: - Ensure articles are published according to internal...

  • Senior Cra

    hace 6 meses


    En remoto, España ICON A tiempo completo

    As a Sr. CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - Act as liaison between the in-house team, vendors, and multiple clinical sites. - Develop strong site relationships, maintaining close contact with sites by telephone,...

  • Senior Project Manager

    hace 6 meses


    En remoto, España ICON A tiempo completo

    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...