Clinical Site Liaison Specialist

7 giorni fa


Roma, Lazio, Italia Pharmiweb A tempo pieno
Job Description

As a Clinical Site Liaison, you will be joining a leading clinical research organization, powered by healthcare intelligence. Your role will be to support the conduct and patient recruitment of global clinical trials at investigative sites.

Key Responsibilities:
  • Study-Level Feasibility: Provide key country/ regional and site specific knowledge, including patient pathways and operational execution.
  • Local Client Representation: Interface and act as a local client TrialOps representative, an expert on the clinical trial protocol(s) and SME providing the sites with knowledge and awareness about the current and upcoming clinical trials.
  • Site Engagement: Lead and engage in local site, KOL and network engagement initiatives in view of the clinical trials.
  • Site Feasibility/ Selection Strategy: Contribute to the trial specific site feasibility / selection strategy and collaborate with the Clinical Trial Team (CTT) and CRO to support the site start-up process as needed.
  • Site Contract Negotiation: Facilitate with the site contract negotiation/signature as needed.
  • Patient Recruitment: Proactively work to fully understand all matters that impact the successful patient recruitment and high quality conduct of the clinical trial at each site.
  • Patient Voice: Proactively work to fully understand the patient voice, preferences and pathway(s).
  • Monitoring Oversight: May participate in monitoring oversight activities such as accompanying the CRO CRA during site visits.
  • Site Engagement Optimization: Optimize site engagement for a specific trial to ensure site engagement and quality for the site-level enrollment and execution of every trial.
  • Patient Recruitment Tracking: Oversee and track patient recruitment for the regional sites and pro-actively identify ways to prevent recruitment delays.
  • Issue Identification and Escalation: Pro-actively identify issues and look for solutions in the assigned clinical trial and timely escalate them to the respective study CTM, CODL, Global Head of Clinical Site Communication, Recruitment and Liaisons, Head of Trial Operations and/or Senior Management, as needed.
  • Efficiency Identification: Identify efficiencies, best practices and lessons learnt and ensure they are shared across trials/indications/compounds.
  • Innovation: Search for and embrace innovation.
  • Clinical Development Strategy: May be asked to provide input to the clinical development strategy/plan.
  • Workstreams and Procedures: Participate in workstreams and provide input to procedures/SOPs/WIs and related documents.
Requirements:
  • Education: Bachelor's degree, Scientific or health related field University degree - medical or para-medical (MD, Biology, Biomedical Sciences, Pharmacy, Veterinary etc.) or equivalent by experience.
  • Experience: Minimum of 6 years of experience in Biotech / pharma preferably in roles including site engagement and / or clinical trial monitoring experience.
  • Travel: Ability for travel nationally and occasional international travel.
  • Global Clinical Trials: Experience in global clinical trials is a plus.
  • Neurology, Auto-immune and rare disease background: Prior experience in Neurology, Auto-immune and rare disease background.
  • ICH-GCP and Legislation: Knowledge of ICH-GCP and other applicable legislation.
  • Communication and Presentation Skills: Excellent communication and presentation skills and relationship management of multiple stakeholders, internally and externally, including sites, KOLs, networks, PAGs, CROs and others.
  • Leadership and Problem Solving: Leadership with the ability to overcome challenges, seek opportunities to remove barriers, influence without authority.
  • Organizational Skills: Highly developed organizational skills, problem solving, analytic and able to prioritize.
  • Tools and Systems: Experience with tools and systems for managing clinical studies.
What ICON Can Offer:

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 maximise 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 website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. 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 through the form below.

https://careers.iconplc.com/reasonable-accommodations

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.



  • Roma, Lazio, Italia Icon Strategic Solutions A tempo pieno

    Job SummaryWe are seeking a highly skilled Clinical Site Liaison to join our team at Icon Strategic Solutions. As a Clinical Site Liaison, you will play a critical role in supporting the conduct and patient recruitment of global clinical trials at investigative sites.Key ResponsibilitiesParticipate in study-level feasibility activities, providing key...


  • Roma, Lazio, Italia Engineeringuk A tempo pieno

    Job DescriptionJob Title: Clinical Site LiaisonJob Summary: We are seeking a highly skilled Clinical Site Liaison to join our team. As a Clinical Site Liaison, you will be responsible for supporting the conduct and patient recruitment of global clinical trials at investigative sites.Key Responsibilities:Participate in study-level feasibility activities,...


  • Roma, Lazio, Italia Pfizer A tempo pieno

    JOB SUMMARY: The Clinical Site Activation Specialist plays a pivotal role in overseeing and facilitating operational tasks from initiation to conclusion for designated studies and investigator locations. This position ensures adherence to study timelines while complying with relevant regulations, Good Clinical Practices, and Pfizer's internal standards....


  • Roma, Lazio, Italia Pfizer A tempo pieno

    JOB SUMMARY: The Clinical Site Activation Specialist plays a pivotal role in overseeing and facilitating operational tasks from initiation to conclusion for designated studies and investigator locations. This position ensures adherence to study timelines while complying with relevant regulations, Good Clinical Practices, and Pfizer's internal standards....


  • Roma, Lazio, Italia Resourcing Life Science A tempo pieno

    Job OverviewAs a Clinical Contract Specialist with Resourcing Life Science, you will play a crucial role in preparing and negotiating site contracts for assigned studies. Your expertise will be essential in monitoring timelines for site contract and budget, as well as serving as a point of contact for Clinical Trial Agreements. Additionally, you will train...


  • Roma, Lazio, Italia Pfizer A tempo pieno

    Job Summary:The Clinical Site Activation Partner is responsible for leading or supporting operational activities from start-up to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and Pfizer standards.Key Responsibilities:Initiate and coordinate...


  • Roma, Lazio, Italia Resourcing Life Science A tempo pieno

    **Job Overview**We are seeking a skilled Clinical Contract Specialist to join our team in Italy. As a key member of our team, you will be responsible for preparing and negotiating site contracts for assigned studies.**Key Responsibilities**Prepare and negotiate site contracts for assigned studiesMonitor timelines for site contract and budgetPoint of contact...


  • Roma, Lazio, Italia Pfizer A tempo pieno

    JOB SUMMARY: The Clinical Trial Activation Lead is tasked with overseeing or assisting operational functions from initiation to completion for designated studies and investigator locations, ensuring adherence to study schedules and compliance with applicable regulations, Good Clinical Practices, and Pfizer's standards. Responsibilities may extend across...


  • Roma, Lazio, Italia Resourcing Life Science A tempo pieno

    Company OverviewResourcing Life Science is proud to partner with a leading Global CRO that offers a full-service solution for clinical and non-clinical development, peri-approval, and market access. Their expertise spans various pharmaceutical and biotech companies globally.Job SummaryWe are seeking a highly skilled Clinical Contract Specialist to join our...


  • Roma, Lazio, Italia PAREXEL A tempo pieno

    About the RoleParexel is seeking a highly skilled Site Alliance Relationship Manager to join our team. As a key member of our Site Alliance team, you will be responsible for building and maintaining strong relationships with our site partners, ensuring seamless execution of clinical trials, and driving business growth.Key ResponsibilitiesAnalyze site...


  • Roma, Lazio, Italia IQVIA A tempo pieno

    Job Overview:As a Clinical Contract Negotiator, you will play a crucial role in developing and implementing contracting strategies to support the delivery of clinical trials. Your expertise will be essential in negotiating contracts with sponsors, ensuring compliance with regulatory requirements, and maintaining strong relationships with stakeholders.Key...


  • Roma, Lazio, Italia IQVIA A tempo pieno

    Job OverviewIQVIA is seeking a highly skilled Clinical Trials Specialist to join our team. As a key member of our Connected Devices Solution, you will be responsible for ensuring the seamless integration of medical devices with our eSource platforms.Key ResponsibilitiesValidate Connected Devices for clinical trials, working closely with vendors and internal...


  • Roma, Lazio, Italia Galderma Pharma S.A A tempo pieno

    Job Title: Medical Science Liaison - Biologics SpecialistGalderma is seeking a Medical Science Liaison - Biologics Specialist to join our team. As a key internal expert, you will provide field-based scientific and clinical support to healthcare professionals to maintain a high level of medical, scientific, and technical knowledge and expertise in relation to...


  • Roma, Lazio, Italia Pfizer A tempo pieno

    Job SummaryThe Site Activation Partner is a critical role within Pfizer's clinical trials team, responsible for leading or supporting operational activities from start-up to close-out. This position ensures compliance with study timelines and prevailing laws, Good Clinical Practices, and Pfizer standards.Key ResponsibilitiesInitiate and coordinate activities...


  • Roma, Lazio, Italia Pfizer A tempo pieno

    Job SummaryPfizer is seeking a highly experienced Senior Director of Clinical Site Operations to join our team. As a key member of our Site Country Operations team, you will play a critical role in delivering strategic vision and representing Pfizer operations at the country or cluster level.The ideal candidate will have a strong background in clinical...


  • Roma, Lazio, Italia Pharmiweb A tempo pieno

    Job Title: Clinical Research Associate IIWe are seeking a highly motivated and detail-oriented Clinical Research Associate II to join our team. As a Clinical Research Associate II, you will be responsible for monitoring and managing clinical sites, ensuring compliance with regulatory requirements and study protocols.Key Responsibilities:Act as liaison...


  • Roma, Lazio, Italia Pfizer A tempo pieno

    Job Summary:The Site Activation Specialist is responsible for leading or supporting operational activities from start-up to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and Pfizer standards. This role may span over more than one country...


  • Roma, Lazio, Italia Pfizer A tempo pieno

    Job SummaryThe Senior Director of Clinical Site Operations is a key leadership role within Pfizer Oncology Division, responsible for delivering strategic vision and representing the company at the country or cluster level.This role requires a dynamic leader who can establish and cultivate relationships with key stakeholders, including KOLs, strategic...


  • Roma, Lazio, Italia Pfizer A tempo pieno

    Job Summary:The Site Activation Partner is responsible for leading or supporting operational activities from start-up to close-out, ensuring compliance with study timelines and Good Clinical Practices. This role requires a strong understanding of clinical trial methodologies, ICH/GCP, and global/local country regulations.Key Responsibilities:Initiate and...


  • Roma, Lazio, Italia Allergan A tempo pieno

    Job SummaryWe are seeking a highly skilled Clinical Research Associate II to join our team at Allergan. As a Clinical Research Associate II, you will be responsible for ensuring the successful execution of clinical studies at investigative sites.Key ResponsibilitiesStudy Site Monitoring: Monitor activities conducted by clinical investigative sites to ensure...