This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description Entravision, one of America’s leading Spanish media companies, is seeking multiple talented Bilingual Editor Producers to join our innovative Luminex team remotely! If you have a passion for storytelling and a knack for creating compelling visual content, we want to hear from you! If you’re ready to elevate your editing career and help us build a new world of media, apply today! Join us in shaping the future of Spanish media. - Edit and produce high quality video content using Adobe Premiere or Final Cut Pro. - Build engaging graphics to enhance storytelling and visual appeal. - Collaborate with a creative team to bring new and groundbreaking ideas to life. - Contribute to the development of compelling narratives that resonate with our audience. - Help shape and build a new world of digital media that pushes boundaries and engages viewers. Qualifications - Bilingual proficiency in English and Spanish. Requirements - Proficiency in video editing software, specifically Adobe Premiere or Final Cut Pro. - Experience in graphic design and the ability to create visually appealing graphics. - A strong creative vision and the ability to generate innovative ideas. - Excellent attention to detail and a passion for storytelling. - Ability to work independently and collaboratively in a fast-paced remote environment. Company Description Entravision is a leading global advertising, media and ad-tech solutions company connecting brands to consumers by representing top platforms and publishers. Our service portfolio enables high-performance campaigns while using highly competitive audience reach, cutting-edge mobile programmatic solutions, machine-learned bidding algorithms and demand-side platforms on a global scale. In the US, Entravision is a leader in Hispanic marketing & media solutions serving both local and national Clients for more than 25 years. Our unique portfolio includes primarily Spanish language TV & Radio broadcast assets across 35 markets, an exclusive audio network & streaming platform, and a robust mix of curated digital & social media content solutions.

Local Trial Manager 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 What you will be doing: - Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality. - Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with Procedural Documents, ICH-GCP and local regulations. - Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality. - Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks. - Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations. - Ensures preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in AZ clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head. - Ensures timely preparation of local Master CSA (including site budget) and amendments as needed. - Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant SOPs and local regulations. - Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with SOPs. - Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction). - Sets up and maintains the study in CTMS at study country level as well as local websites as required by local laws and regulations. - Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans. - Reviews monitoring visit reports (as required and following SOPs) and pro-actively advices the monitor(s) on study related matters. - Performs any required co-monitoring, Accompanied Site Visits/training visits with study CRAs. - Proactively identifies risks and facilitates resolution of complex study problems and issues. - Organizes regular Local Study Team meetings on an agenda driven basis. - Actively works towards achieving good personal relationships with all Local Study Team members, sites’ staff and global stakeholders. - Reports study progress/update to the Global Study Associate Director/ Global Study Team including SMM Lead. - Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary. - Develops, maintains and reviews risk management plan on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. - Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable. - Plans and leads National Investigator meetings, in line with local codes, as required. - Assists in forecasting study timelines, resources, recruitment, budget, study materials and drug supplies. - Ensures relevant systems required to facilitate business critical, license to operate activities (for example, Safety Reporting, Regulatory submissions, Clinical Trial Transparency) are set-up, updated and access is organised at country level. - Ensures accurate payments related to the study are performed according to local regulations and agreements. - Participates in training and coaching new members of the Local Study Team ensuring compliance with ICH-GCP and Procedural Documents. - Ensures completeness of the eTMF and ensures essential documents are uploaded in a timeline bmanner to maintain the eTMF “Inspection Ready”. - Ensures that all study documents are ready for final archiving and completion of local part of the eTMF. - Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and QA. - Provides input to process development and improvement. - Provides regular information to Line Managers at country level on study/ies and planned study milestones/key issues. - Updates Line Managers about the performance of the CRAs/CSAs. - Ensures that study activities at country level comply with local policies and code of ethics. - Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market. - Ensures compliance with company Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment). - Collaborates with local Medical Affairs team. Your profile: - Bachelor degree in related discipline, preferably in life science, or equivalent qualification (*). - Five years of US focused clinical trial management experience, including budget oversight - Good knowledge of international guidelines ICH- GCP as well as relevant local regulations. - Excellent project management skill - Excellent team building and interpersonal skills - Excellent organisational skills - Excellent verbal and written communication skills - Excellent ability to prioritize and handle multiple tasks - Excellent attention to details - Excellent knowledge of spoken and written English - Good ability to learn and to adapt to work with IT systems. - Location: US remote What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Local Study Associate Director 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 What you will be doing: - Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality. - Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with Procedural Documents, ICH-GCP and local regulations. - Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality. - Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks. - Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations. - Ensures preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in AZ clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head. - Ensures timely preparation of local Master CSA (including site budget) and amendments as needed. - Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant SOPs and local regulations. - Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with SOPs. - Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction). - Sets up and maintains the study in CTMS at study country level as well as local websites as required by local laws and regulations. - Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans. - Reviews monitoring visit reports (as required and following SOPs) and pro-actively advices the monitor(s) on study related matters. - Performs any required co-monitoring, Accompanied Site Visits/training visits with study CRAs. - Proactively identifies risks and facilitates resolution of complex study problems and issues. - Organizes regular Local Study Team meetings on an agenda driven basis. - Actively works towards achieving good personal relationships with all Local Study Team members, sites’ staff and global stakeholders. - Reports study progress/update to the Global Study Associate Director/ Global Study Team including SMM Lead. - Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary. - Develops, maintains and reviews risk management plan on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. - Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable. - Plans and leads National Investigator meetings, in line with local codes, as required. - Assists in forecasting study timelines, resources, recruitment, budget, study materials and drug supplies. - Ensures relevant systems required to facilitate business critical, license to operate activities (for example, Safety Reporting, Regulatory submissions, Clinical Trial Transparency) are set-up, updated and access is organised at country level. - Ensures accurate payments related to the study are performed according to local regulations and agreements. - Participates in training and coaching new members of the Local Study Team ensuring compliance with ICH-GCP and Procedural Documents. - Ensures completeness of the eTMF and ensures essential documents are uploaded in a timeline bmanner to maintain the eTMF “Inspection Ready”. - Ensures that all study documents are ready for final archiving and completion of local part of the eTMF. - Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and QA. - Provides input to process development and improvement. - Provides regular information to Line Managers at country level on study/ies and planned study milestones/key issues. - Updates Line Managers about the performance of the CRAs/CSAs. - Ensures that study activities at country level comply with local policies and code of ethics. - Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market. - Ensures compliance with company Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment). - Collaborates with local Medical Affairs team. Your profile: - Bachelor degree in related discipline, preferably in life science, or equivalent qualification (*). - Five years of US focused clinical trial management experience, including budget oversight - Good knowledge of international guidelines ICH- GCP as well as relevant local regulations. - Excellent project management skill - Excellent team building and interpersonal skills - Excellent organisational skills - Excellent verbal and written communication skills - Excellent ability to prioritize and handle multiple tasks - Excellent attention to details - Excellent knowledge of spoken and written English - Good ability to learn and to adapt to work with IT systems. - Location: US remote What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

Local Trial Manager 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 What you will be doing: - Has the overall responsibility for the study commitments within the country and for timely delivery of data to required quality. - Leads and optimizes the performance of the Local Study Team(s) at country level ensuring compliance with Procedural Documents, ICH-GCP and local regulations. - Ensures, as required, that clinical and operational feasibility assessment of potential studies is performed to the highest quality. - Coordinates the site selection process by identifying potential sites/investigators, performing initial Site Quality Risk Assessment, and conducting Site Qualification Visits to evaluate suitability and quality risks. - Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations. - Ensures preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budget in AZ clinical studies financial system by regular checks of the system and financial reports (as agreed with Director, SMM/ Director, Country Head. - Ensures timely preparation of local Master CSA (including site budget) and amendments as needed. - Ensures timely preparation of country level Master Informed Consent Form (MICF) and subsequent site level ICFs, as required, including any relevant translations, and in line with relevant SOPs and local regulations. - Ensures all country and site level trial essential documents required by ICH-GCP prior to study start have been collected and verified for correctness, prior to setting sites ready to enrol, and in line with SOPs. - Plans and coordinates applicable local drug activities (from local purchase or reimbursement to drug destruction). - Sets up and maintains the study in CTMS at study country level as well as local websites as required by local laws and regulations. - Oversees, manages and coordinates monitoring activities from site activation through to study closure at country and site level in accordance with the Monitoring Plans. - Reviews monitoring visit reports (as required and following SOPs) and pro-actively advices the monitor(s) on study related matters. - Performs any required co-monitoring, Accompanied Site Visits/training visits with study CRAs. - Proactively identifies risks and facilitates resolution of complex study problems and issues. - Organizes regular Local Study Team meetings on an agenda driven basis. - Actively works towards achieving good personal relationships with all Local Study Team members, sites’ staff and global stakeholders. - Reports study progress/update to the Global Study Associate Director/ Global Study Team including SMM Lead. - Contributes to patient recruitment strategy including regular communication with participating Investigators as necessary. - Develops, maintains and reviews risk management plan on country study level: proactively manages sites, stakeholders, local and global vendors and customers to ensure risks are timely identified, mitigated and managed. - Communicates and co-ordinates regularly with National Co-ordinating Investigator / National Lead Investigator on recruitment and other study matters, if applicable. - Plans and leads National Investigator meetings, in line with local codes, as required. - Assists in forecasting study timelines, resources, recruitment, budget, study materials and drug supplies. - Ensures relevant systems required to facilitate business critical, license to operate activities (for example, Safety Reporting, Regulatory submissions, Clinical Trial Transparency) are set-up, updated and access is organised at country level. - Ensures accurate payments related to the study are performed according to local regulations and agreements. - Participates in training and coaching new members of the Local Study Team ensuring compliance with ICH-GCP and Procedural Documents. - Ensures completeness of the eTMF and ensures essential documents are uploaded in a timeline bmanner to maintain the eTMF “Inspection Ready”. - Ensures that all study documents are ready for final archiving and completion of local part of the eTMF. - Plans and leads activities associated with audits and regulatory inspections in liaison with CQAD and QA. - Provides input to process development and improvement. - Provides regular information to Line Managers at country level on study/ies and planned study milestones/key issues. - Updates Line Managers about the performance of the CRAs/CSAs. - Ensures that study activities at country level comply with local policies and code of ethics. - Provides feedback on any research related information including sites/investigators/competing studies that might be useful for the local market. - Ensures compliance with company Code of Ethics, company policies and procedures relating to people, finance, technology, security and SHE (Safety, Health and Environment). - Collaborates with local Medical Affairs team. Your profile: - Bachelor degree in related discipline, preferably in life science, or equivalent qualification (*). - Five years of US focused clinical trial management experience, including budget oversight - Good knowledge of international guidelines ICH- GCP as well as relevant local regulations. - Excellent project management skill - Excellent team building and interpersonal skills - Excellent organisational skills - Excellent verbal and written communication skills - Excellent ability to prioritize and handle multiple tasks - Excellent attention to details - Excellent knowledge of spoken and written English - Good ability to learn and to adapt to work with IT systems. - Location: US remote What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: - Various annual leave entitlements - A range of health insurance offerings to suit you and your family’s needs. - Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. - Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. - Life assurance - Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply