Clinical Project Manager

1 week ago


Athens, Attica, Greece IQVIA Full time €35,000 - €60,000 per year

Job OverviewProject Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. Clinical Project leads can run their own studies. The Project Lead focus is on leveraging therapeutic expertise and IQVIA's suite of solutions to drive operational excellence and strategic leadership with our customers.Essential Functions• Participate in bid defense presentations in partnership with Business Development and may lead the presentation for smaller, less complex regional studies.• May be responsible for delivery and management of smaller, less complex, regional studies.• Develop integrated study management plans with the core project team.• Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.• Set objectives of the core project team and/or sub-team(s) according to agreed upon contract, strategy and approach, effectively communicate and assess performance.• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.• Monitor progress against contract and prepare/present project and/or sub-team information proactively to stakeholders internally and externally.• Manage risk (positive and negative) and contingencies proactively and lead problem solving and resolution efforts.• Achieve project quality by identifying quality risks and issues, responding to issues raised by project team and/or sub-team members and planning/implementing appropriate corrective and preventative action plans.• May serve as primary or backup project contact with customer and would then own the relationship with the project's key customer contacts, as well as communicate/collaborate with IQVIA business development representatives, as necessary.;• Build the cross-functional project team and lead their efforts; responsible for managing cross-collaboration of the core team and for overall project delivery to support milestone achievement and to manage study issues and obstacles.;• Ensure the financial success of the project.• Forecast and identify opportunities to accelerate activities to bring revenue forward.• Identify changes in scope and manage change control process as necessary.• Identify lessons learned and implement best practices.• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements.;• Adopt corporate initiatives and changes and serve as a change advocate when necessary.• Provide input to line managers of their 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 development.Qualifications• Bachelor's Degree Life sciences or related field Req• 5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience. Req• Advanced knowledge of job area, and broad knowledge of other related job areas, typically obtained through advanced education combined with experience. Req• 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 the competitive environment and how to communicate/demonstrate value through IQVIA solutions.;• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.• Problem solving - Strong problem solving skills.• Leadership - Ability to work through others to deliver results to the 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.• Leadership - Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.• Organisation - 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.• Prioritisation - Ability to handle conflicting priorities.• Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.• Quality - Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.• IT skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.• Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.• Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.• Finances - Good understanding of project financials including experience managing, contractual obligations and implications.• IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).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 and population health worldwide. Learn more



  • Athens, Attica, Greece IQVIA Full time €45,000 - €90,000 per year

    Clinical Trial Manager - IQVIA Biotech * Please note: due to sponsor requirements for the role only candidates based in the listed location/s and with previous Global CTM experience will be considered. Any applications from candidates based outside of these locations will not be considered.Job OverviewClinical Trial Managers (CTM) are an integral part of...


  • Athens, Attica, Greece ICON plc Full time €50,000 - €150,000 per year

    Manager Clinical OperationsICON 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 developmentWe are currently seeking a Manager, Clinical Operations to join our diverse...


  • Athens, Attica, Greece ICON plc Full time €110,000 - €170,000 per year

    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.We are currently seeking a Manager, Clinical Operations to join our diverse and dynamic team. As a...


  • Athens, Attica, Greece Fortrea Full time €25,000 - €45,000 per year

    Job Overview:The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned....


  • Athens, Attica, Greece Fortrea Full time €50,000 - €80,000 per year

    Job OverviewThe Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation of project plans, as assigned. Function as leader for projects of limited scope, as assigned. Assume...

  • Clinic Coordinator

    6 days ago


    Athens, Attica, Greece AT Skin Clinic Ιατρική ΜΟΝ ΙΚΕ Full time €25,000 - €40,000 per year

    Short DescriptionManaging daily operations at a medical clinic, including patient scheduling, call answering, and coordination between medical doctors and patients. Ensures smooth workflow, excellent patient service, and adherence to clinic protocols.Medical Secretary / Clinical Coordinator (Athens & Remote Support for London Clinic)We are looking for a...


  • Athens, Attica, Greece Pfizer Full time

    Role SummaryAs part of the Clinical Data & Information Sciences (CDIS) group, an integral delivery unit within the Clinical Development & Operations (CD&O) organization, the Asset Lead is responsible for timely and high-quality data management deliverables supporting the Pfizer portfolio. Responsibilities include delivery of asset level information...


  • Athens, Attica, Greece IQVIA Full time €50,000 - €80,000 per year

    Job OverviewPerform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.Essential Functions• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with...


  • Athens, Attica, Greece IQVIA Full time €48,000 - €72,000 per year

    Clinical Specialist Consultant - Greek Speaking Location:  Remote/virtualHours:  Estimated 10-16h/monthRole:  Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. The quality of assessments is...


  • Athens, Attica, Greece IQVIA Full time

    Clinical Specialist Consultant - Greek SpeakingLocation: Remote/virtualHours: Estimated 10-16h/monthRole: Clinical SpecialistJob Description:The Clinical Specialist reviews scales administered by raters in a clinical trial to ensure that assessments are being conducted in a standardized manner to ensure data reliability. The quality of assessments is...