Aktualne oferty pracy związane z Clinical Trial Project Manager - Warszawa, Mazovia - IQVIA Argentina


  • Warszawa, Mazovia, Polska TN Poland Pełny etat

    Clinical Trial Manager II, Dermatology & RheumatologyJob Summary:The Clinical Trial Manager II (CTM II) is responsible for the operational management and oversight of clinical investigative sites as well as clinical monitoring deliverables of clinical trials.Responsibilities:Ensures timely quality deliverables and in accordance with applicable standard...


  • Warszawa, Mazovia, Polska Rho, Inc. Pełny etat

    About the RoleWe are currently hiring a Freelance Clinical Project Manager to work remotely on a freelance basis, managing international Phase I-IV clinical trials.The successful candidate will have excellent leadership and organizational skills, with a proven track record of delivering projects on time and within budget.Main ResponsibilitiesManage...


  • Warszawa, Mazovia, Polska Hays Poland Pełny etat

    Clinical Data Manager RoleHays Poland invites applications from motivated professionals looking to take on a new challenge as a Clinical Data Manager.The ideal candidate will have extensive knowledge of clinical data management principles, methods, and regulations, coupled with hands-on experience in implementing data management plans and overseeing data...


  • Warszawa, Mazovia, Polska Rho Pełny etat

    Job Description:We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our Clinical Operations team in Poland, Estonia, Lithuania, or Latvia. The successful candidate will have experience in Clinical Trials and possess excellent organizational, communication, and teamwork skills.Key Responsibilities:Preparation of ISFs...


  • Warszawa, Mazovia, Polska Rho, Inc. Pełny etat

    Job SummaryRho, Inc. is seeking a highly experienced Freelance Clinical Project Manager to join our team in the EU.This is a remote position working on a freelance basis, requiring strong leadership and organizational skills to manage international Phase I-IV clinical trials.Key ResponsibilitiesManage clinical study budgets and create/update project plans...


  • Warszawa, Mazovia, Polska PSI CRO Pełny etat

    Are you an expert in graphic design looking to apply your skills in a fast-paced environment? Do you have a passion for creating visually appealing documents?We're seeking a highly skilled Clinical Trial Document Specialist to join our team at PSI CRO. As a specialist, you'll be responsible for designing and developing clinical trial documents that meet...

  • Clinical Trial Lead

    6 dni temu


    Warszawa, Mazovia, Polska PSI CRO Pełny etat

    Job DescriptionWe are seeking a highly skilled Clinical Trial Lead to join our team at PSI CRO. As a Central Monitoring Manager, you will be responsible for leading the implementation of risk-based monitoring approaches on clinical study and program levels.You will:Facilitate initial and ongoing study Risk Management activities.Participate in the selection...


  • Warszawa, Mazovia, Polska Rho Pełny etat

    OverviewJoin us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges.At Rho, we're committed to you just as you're committed to us. You'll have the opportunity to...


  • Warszawa, Mazovia, Polska Rho, Inc. Pełny etat

    OverviewJoin us in redefining what it means to work for a CRO. Working at Rho, you'll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity's biggest challenges.At Rho, we're committed to you just as you're committed to us. You'll have the opportunity to...


  • Warszawa, Mazovia, Polska IQVIA Pełny etat

    Role Summary:We are seeking a skilled Clinical Trial Vendor Manager to join our team. This individual will be responsible for managing vendor relationships, coordinating study start-up activities, and monitoring vendor performance to ensure timely delivery of high-quality services.Key Responsibilities:Develop and maintain strong relationships with vendors to...


  • Warszawa, Mazovia, Polska TN Poland Pełny etat

    TN Poland is seeking a detail-oriented and organized individual to fill the role of Associate Site Manager.Responsibilities:The Associate Site Manager will be responsible for ensuring site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases.This role also involves contributing to site...


  • Warszawa, Mazovia, Polska TN Poland Pełny etat

    The Clinical Trial Support Coordinator role at TN Poland involves providing support to clinical trial teams through troubleshooting, problem identification, solution identification and resolution.Key ResponsibilitiesProvide technical support to clinical trial teams.Collaborate with cross-functional teams to resolve issues.Analyze data to identify trends and...


  • Warszawa, Mazovia, Polska TN Poland Pełny etat

    Transforming lives through clinical research is at the core of our mission at Thermo Fisher Scientific. As a leading global contract research organization, we are dedicated to improving health outcomes that people and communities depend on. Our purpose is to help customers deliver life-changing therapies, and our strategy is to bend the cost and time curve...


  • Warszawa, Mazovia, Polska TN Poland Pełny etat

    About the Role:The Global Study Manager will be responsible for managing clinical studies from initiation to closure, ensuring timely delivery, within budget and to the required quality standards.This role will involve working cross-functionally with internal and external partners to deliver delegated aspects of the clinical study in accordance with the...


  • Warszawa, Mazovia, Polska IQVIA Pełny etat

    Job Summary:We are seeking a skilled Clinical Trial Vendor Manager to oversee vendor performance and ensure timely delivery of high-quality services at the study level. The ideal candidate will have extensive experience in clinical operations processes, excellent vendor management skills, and strong project management abilities.Key...


  • Warszawa, Mazovia, Polska Rho Pełny etat

    OverviewRho is a global contract research organization (CRO) dedicated to healthcare and clinical research. We take a personalized approach to working with our clients, understanding their unique needs and challenges.We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our team in Poland, Estonia, Lithuania, or Latvia. As a...


  • Warszawa, Mazovia, Polska Rho, Inc. Pełny etat

    OverviewJoin us in redefining what it means to work for a CRO. Dokumeds has become part of Rho, an award-winning, full-service CRO based in North America. As one company, we will deliver global full-service clinical development services and unmatched customer support – worldwide. Working at Rho, you'll be joining a team who take healthcare and clinical...


  • Warszawa, Mazovia, Polska IQVIA Pełny etat

    Job SummaryThis is an exciting opportunity to join our team at IQVIA as a Trial Master File Manager. The successful candidate will be responsible for managing TMFs and other related documents, ensuring compliance with applicable SOPs, processes, and study-specific requirements.Main AccountabilitiesManage TMFs and other related documents from creation through...


  • Warszawa, Mazovia, Polska Rho Pełny etat

    We are seeking a highly skilled Freelance Regional Clinical Trial Coordinator to join our Clinical Operations team in Poland, Estonia, Lithuania, or Latvia. The successful candidate will have experience in Clinical Trials and possess excellent organizational, communication, and teamwork skills.Key Responsibilities:Preparation of ISFs (Investigator Site...


  • Warszawa, Mazovia, Polska Rho, Inc. Pełny etat

    Job DescriptionRho, Inc. is a leading Contract Research Organization (CRO) with a global presence.We are seeking a highly experienced Freelance Clinical Project Manager to join our team in the EU, working on a freelance basis to manage international Phase I-IV clinical trials.Main DutiesManage clinical studies from start to finish, ensuring compliance with...

Clinical Trial Project Manager

1 tydzień temu


Warszawa, Mazovia, Polska IQVIA Argentina Pełny etat

Job Overview

Clinical trials are a crucial part of bringing new drugs to the market faster, and at IQVIA Argentina, we're looking for a skilled Tactical and Operational Scientific Co-Ordinator to join our team. As a key member of our clinical trial delivery team, you'll work closely with clinical teams to improve patient outcomes.

Essential Functions:

  • Participate in bid defense presentations, collaborating with Business Development and leading presentations for smaller, less complex regional studies.
  • Manage smaller, less complex, regional studies, ensuring timely and cost-effective delivery.
  • Develop integrated study management plans with core project teams.
  • Oversee the execution of clinical studies, optimizing speed, quality, and cost while maintaining compliance with standard processes and policies.
  • Set objectives for core project teams and/or sub-teams according to agreed-upon contracts, strategies, and approaches, effectively communicating and assessing performance.
  • Collaborate with other functional groups within the company to support milestone achievement and manage study issues and obstacles.
  • Monitor progress against contract requirements and present project information proactively to stakeholders internally and externally.
  • Proactively manage risk and contingencies, leading problem-solving and resolution efforts.
  • Achieve project quality by identifying quality risks and issues, responding to concerns raised by project teams and/or sub-team members, and planning/implementing corrective and preventative action plans.
  • Serve as primary or backup project contact with customers, owning relationships with project's key customer contacts, and communicate/collaborate with IQVIA business development representatives as necessary.
  • Build cross-functional project teams, leading their efforts; responsible for managing cross-collaboration of core teams and overall project delivery to support milestone achievement and manage study issues and obstacles.
  • Ensure financial success of projects, forecasting revenue and identifying opportunities to accelerate activities to bring revenue forward.
  • Identify changes in scope and manage change control processes as necessary.
  • Identify lessons learned and implement best practices.
  • May be assigned as primary contact for vendors, leading project vendor management and vendor management-related activities as per project requirements.
  • Acknowledge and adapt to corporate initiatives and changes, serving as a change advocate when necessary.
  • Provide input to line managers on project team members' performance relative to project tasks.
  • Support staff development and mentor less experienced project team members on assigned projects to support their professional growth.

Qualifications:

  • Bachelor's Degree in Life Sciences or related field.
  • 5 years of prior relevant experience, including > 1 year of project management experience or equivalent combination of education, training, and experience.
  • Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience.
  • Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations, and guidelines, towards clinical trial conduct.
  • Broad protocol knowledge; therapeutic knowledge desired. Good understanding of competitive environment and how to communicate/demonstrate value through IQVIA solutions.
  • Strong written and verbal communication skills, including good command of English language. Strong presentation skills.
  • Strong problem-solving skills.
  • Ability to work through others to deliver results to appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross-functionally and with customers to advance work effectively and efficiently.
  • Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.
  • Planning, time management, and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives, and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.
  • Ability to handle conflicting priorities.
  • Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.
  • Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.
  • Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel, and PowerPoint.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients. Strong customer service skills.
  • Ability to work across geographies displaying high awareness and understanding of cultural differences.
  • Good understanding of project financials including experience managing contractual obligations and implications.
  • Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, Innovation, Ownership).