jobs in IQVIA

IQVIA

50-200 Employees · IT / Software ·

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67 Job Vacancies

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IQVIA Job Vacancies and Careers

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Hong Kong

  • R1568038Responsibilities
  • Lead study strategy developmentPartner with Sales, Medical, and Operations teams to develop competitive and operationally feasible solutions for client opportunities.Provide expertise in protocol assessment, feasibility strategy, site and country selection, patient recruitment, and study execution planning.Support proposal development, bid defense meetings, and client presentations.Ensure effective transition of study strategy to project delivery teams and provide strategic guidance throughout study execution.
  • Qualifications ...
Posted
2 days ago
WFH

Hong Kong

  • R1565543Global Project Leadership Team (Oncology)Key ResponsibilitiesLead the end-to-end delivery of complex global oncology clinical studies and programs, ensuring quality, timelines, budgets, and customer satisfaction.Serve as the primary point of contact for sponsors and stakeholders, building strong client relationships and managing expectations throughout the project lifecycle.Drive cross-functional global teams to achieve study milestones, proactively identify and mitigate risks, and resolve operational challenges.Lead complex multinational and multi-regional clinical trials (MRCTs), ensuring successful execution across regions including China, the US, and Europe.Influence and drive results across a global matrix organization without direct reporting authority.Support business development activities, including RFP responses, bid defenses, client presentations, and strategic account growth initiatives.Partner with sponsors to understand development strategies and deliver tailored project solutions.Contribute to client retention, expansion, and new business opportunities.Requirements10+ years of project management experience within CRO, pharmaceutical, or biotechnology organizations, including 7+ years independently leading global clinical projects/programs.Strong oncology clinical trial experience is required.Proven track record serving as a Project Lead (PL) for complex global and multi-regional clinical studies (MRCTs).Fluent in English and Mandarin.
  • 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 at https://jobs.iqvia.com
  • IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. ...
Posted
2 days ago

Singapore

  • Identify, escalate, and support the timely resolution of patient safety, quality, and data integrity issues, including oversight of investigations, corrective actions, and proficiency testing programs.
  • Review and approve validation plans, protocols, and reports for new assays and testing methodologies prior to implementation in the production environment.
  • Support the transition of clinical trial assays from development into routine testing operations and ensure appropriate technical and operational procedures are established and maintained. ...
Posted
3 days ago

KL City

  • Support proposal development, bid defense meetings, and client presentations.
  • Ensure effective transition of study strategy to project delivery teams and provide strategic guidance throughout study execution.
  • Bachelor's degree or above in Life Sciences, Pharmacy, Medicine, Public Health, or a related field. ...
Posted
4 days ago

KL City

  • Support proposal development, bid defense meetings, and client presentations.
  • Ensure effective transition of study strategy to project delivery teams and provide strategic guidance throughout study execution.
  • Bachelor's degree or above in Life Sciences, Pharmacy, Medicine, Public Health, or a related field. ...
Posted
4 days ago

Singapore

  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
  • You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You will need to have a good knowledge of applicable clinical research regulatory requirements. ...
Posted
8 days ago

Singapore

  • Ability to manage multiple tasks and meet deadlines with guidance and support.
  • Experience in an office or administrative environment, or an equivalent combination of education and experience.
  • Regular use of a computer and keyboard for extended periods. ...
Posted
9 days ago

Singapore

  • Lead complex multinational and multi-regional clinical trials (MRCTs), ensuring successful execution across regions including China, the US, and Europe.
  • Influence and drive results across a global matrix organization without direct reporting authority.
  • Support business development activities, including RFP responses, bid defenses, client presentations, and strategic account growth initiatives. ...
Posted
9 days ago

Singapore

  • ELISA testing & Immunoassay systems
  • Perform and document laboratory testing and analytical procedures in compliance with company and regulatory standards.
  • Analyze data, identify unusual results, and escalate issues when necessary. ...
Posted
9 days ago

KL City

  • Develop, finalize, and review master and country-specific subject information sheets (SIS)/ICFs.
  • Review and translate drug labels.
  • Perform independent quality review of submission packages. ...
Posted
9 days ago