Clinical Trials Project Coordinator

2 meses atrás


Lisboa, Lisboa, Portugal Icon Plc Tempo inteiro

About ICON Plc


ICON Plc is a world-leading healthcare intelligence and clinical research organization, fostering an inclusive environment that drives innovation and excellence.


We are proud to be at the forefront of shaping the future of clinical development, working collaboratively with customers to advance and improve patients' lives.



About the Role


We are seeking an experienced Clinical Trials Project Coordinator to join our team. This role will involve managing routine customer communication, developing project timelines, and ensuring adherence to timelines.


The successful candidate will act as the primary point of contact for customers on assigned projects, providing customer support throughout the life cycle of a project.


This position requires strong organizational skills, excellent communication, and problem-solving abilities.



Key Responsibilities:



  • Customer Communication: Manage routine customer teleconferences and generate accurate records and meeting minutes in accordance with regulatory guidelines.
  • Project Management: Develop project plans and timelines via internal and external kick-off meetings, ensuring agreement by parties involved.
  • Revenue Forecasting: Complete revenue forecasting and invoicing per process on-time and accurately.
  • Cross-Functional Teams: Coordinate cross-functional teams to ensure efficient processing of project requirements.
  • Travel: Travel possibly required up to 20% of the time.


Requirements:


To be successful in this role, you will need:



  • Education: Minimum bachelor's degree (preference in Life Sciences or similar) or equivalent education/work experience.
  • Relevant Work Experience: Required minimum of three years in a customer-focused role. Desired minimum of one year working in a project management role within the clinical trial industry.
  • Language: Advanced English fluency required for business communication.


What We Offer:


As a valued member of our team, you can expect a competitive salary of $75,000 - $90,000 per annum, depending on experience, plus various benefits, including:



  • Variety of 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 professionals who are there to support you and your family's well-being.
  • Life assurance.
  • Flexible country-specific optional benefits.

At ICON Plc, we are 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.



  • Lisboa, Lisboa, Portugal Fortrea Tempo inteiro

    OverviewFortrea, a leading global contract research organization, offers a unique opportunity for a skilled Clinical Trials Project Manager to join our team. With a passion for scientific rigor and decades of clinical development experience, we provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development,...


  • Lisboa, Lisboa, Portugal Phiture Tempo inteiro

    Job OverviewWe are seeking a highly skilled Clinical Trials Project Manager to lead our site management efforts in the development of life-changing therapies.As a Clinical Trials Project Manager, you will be responsible for overseeing the implementation of clinical trial projects from initiation to close-out. Your expertise will be crucial in ensuring...


  • Lisboa, Lisboa, Portugal Iqvia Argentina Tempo inteiro

    About the RoleClinical Trial Administrators at Iqvia Argentina play a vital role in ensuring the success of our clinical trials. As a Sr Clinical Trial Assistant/Start-Up, you will be responsible for coordinating and administering daily administrative activities to ensure a complete and accurate Trial Master File delivery.Key Responsibilities:Assist Clinical...


  • Lisboa, Lisboa, Portugal Fortrea Tempo inteiro

    Job SummaryWe are seeking a highly motivated and experienced Clinical Trials Project Manager to join our team at Fortrea. The successful candidate will be responsible for site monitoring, site management, and ensuring the integrity of clinical trials.Responsibilities:Responsible for all aspects of study site monitoring, including routine monitoring and...


  • Lisboa, Lisboa, Portugal Fortrea Tempo inteiro

    About Us: Fortrea is a leading global contract research organization (CRO) dedicated to revolutionizing the development process for pharmaceutical, biotechnology, and medical device customers. With decades of clinical development experience and a passion for scientific rigor, we provide a wide range of clinical development, patient access, and technology...


  • Lisboa, Lisboa, Portugal Mygwork - Lgbtq+ Business Community Tempo inteiro

    Unlock your potential as a Senior Clinical Study Manager at Mygwork - LGBTQ+ Business Community, where diversity and inclusion thrive. We are seeking an experienced professional to lead clinical trials with moderate complexity, providing quality oversight and driving decision-making.Job SummaryAs a Senior Clinical Study Manager, you will be responsible for...


  • Lisboa, Lisboa, Portugal Icon Plc Tempo inteiro

    ICON plc is a world-leading healthcare intelligence and clinical research organization. Our mission is to shape the future of clinical development.We're looking for a Senior Clinical Trial Operations Manager to join our team in EMEA. As a key member of our team, you will be responsible for advancing clinical trial start-up activities by understanding client...


  • Lisboa, Lisboa, Portugal Thermo Fisher Scientific Tempo inteiro

    About the RoleWe are seeking a Clinical Trial Regulatory Affairs Specialist to join our global Regulatory Affairs department – Regulatory Science team. This is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting.Job DescriptionIn this role, you will be a pivotal team member with regulatory...

  • Clinical Trials Statistician

    3 semanas atrás


    Lisboa, Lisboa, Portugal Mai Fortrea Development Limited Tempo inteiro

    Company OverviewMai Fortrea Development Limited is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20...


  • Lisboa, Lisboa, Portugal Mygwork Tempo inteiro

    Unlock Your Potential in Clinical ResearchAre you a highly skilled and experienced Clinical Research Associate looking for a new challenge? Do you want to work with a leading pharmaceutical company that values innovation and collaboration?We are seeking a Senior Clinical Operations Coordinator to join our team in Portugal. As a key member of our clinical...


  • Lisboa, Lisboa, Portugal Thermo Fisher Scientific Tempo inteiro

    Thermo Fisher Scientific, a leading global biotechnology company, is seeking an experienced Regulatory Affairs Specialist to join our Global Clinical Trial team. With a competitive salary of $120,000 per annum, this role offers a unique opportunity to contribute to the development and implementation of regulatory strategies for clinical trials...


  • Lisboa, Lisboa, Portugal Engineeringuk Tempo inteiro

    Job SummaryWe are seeking a highly skilled Clinical Trials Specialist - Contract Negotiator to join our team at ICON plc. In this role, you will play a vital part in driving the costings and contracts for clinical trials, responsible for negotiation and budgeting.About UsICON plc is a world-leading healthcare intelligence and clinical research organisation....


  • Lisboa, Lisboa, Portugal Iqvia Llc Tempo inteiro

    **Job Title:** Regulatory Manager, Clinical Trials Regulatory Expert**Overview of the Company:IQVIA LLC is a leading healthcare technology and consulting company that accelerates innovation in the life sciences through its platform capabilities. Our innovative solutions help healthcare professionals manage data, discover new insights, and develop...


  • Lisboa, Lisboa, Portugal Phiture Tempo inteiro

    Company Overview: At Thermo Fisher Scientific, we're committed to making a positive impact on the world. Our Mission is to enable our customers to make the world healthier, cleaner and safer.Salary: We offer a competitive salary of $80,000 per year, along with an annual incentive plan bonus and a range of employee benefits.Job Description:We're seeking a...


  • Lisboa, Lisboa, Portugal Fortrea Tempo inteiro

    Job Summary">We are seeking a highly motivated Senior Clinical Research Associate II to join our global clinical trial management team. As a key member of the team, you will be responsible for site monitoring and site management for clinical studies according to Fortrea Standard Operating Procedures and Regulatory Guidelines.">About the Role">The Senior...


  • Lisboa, Lisboa, Portugal Mai Fortrea Development Limited Tempo inteiro

    Company Overview">At Mai Fortrea Development Limited, we are a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more...

  • Project Support Coordinator

    3 semanas atrás


    Lisboa, Lisboa, Portugal Iqvia Argentina Tempo inteiro

    Job Title: Project Support CoordinatorAbout Us:IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes...


  • Lisboa, Lisboa, Portugal Icon Plc Tempo inteiro

    Project OverviewWe are seeking a seasoned Senior Clinical Project Lead to join our team at ICON Plc, a world-leading healthcare intelligence and clinical research organization.


  • Lisboa, Lisboa, Portugal Syneos Health Tempo inteiro

    At Syneos Health, we are looking for an experienced MEDICAL WRITER to join our team in leading complex clinical projects from start to finish.We offer a competitive salary of $$95,000 - $115,000 per year, depending on experience, and a comprehensive benefits package that includes health insurance, retirement savings, and paid time off.About the Role:This is...


  • Lisboa, Lisboa, Portugal Tfs Healthscience Tempo inteiro

    **About the Company**TFS HealthScience is a global Contract Research Organization (CRO) dedicated to partnering with biotechnology and pharmaceutical companies throughout their entire clinical development journey. With expertise in full-service capabilities, resourcing, and Functional Service (FSP) solutions, we are seeking a talented Senior Clinical...