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Feasibility and Site ID Lead

IQVIA Holdings Inc.

Hanoi, Vietnam

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

RESPONSIBILITIES

  • Manage and lead activities associated with Feasibility and/or Site Identification for regional and country projects for the larger or more complex trial opportunities.
  • Secure site partnerships and alliances to improve the experiences of our customers and the patients. Accountable for non-project issues such as site business strategy, infrastructure and capabilities, mutual recruitment pipelines, achieving patient recruitment and performance results for assigned sites.
  • Manage assigned opportunities / project / program and adhere to timelines and budget.
  • Support project efforts through data mining of internal databases, review of investigators for quality assurance and development of prioritize site list based on historic site performance and capability
  • Provide information such as disease prevalence, IQVIA’ experience in various therapeutic areas, standard of care, availability / registration status / reimbursement status / price of drugs etc. to relevant parties as necessary or upon request
  • Reconcile and interpret feasibility data. Extrapolate data collected to provide a country-level assessment.
  • Provide accurate, robust and realistic recommendations for country site numbers, recruitment rates, timelines and screen failure rates.
  • May liaise with internal and external customers to coordinate the collection and delivery of feasibility data.
  • Distribute, track, negotiate and review the Confidential Disclosure Agreements (CDAs) with assistance from Management / Legal department as appropriate.
  • Manage the investigator database entry and quality, ensuring complete investigator and site information is captured, monitor for duplicate entries.
  • Track all communications with sites in IQVIA Databases, ensure status of documents is updated in real time
  • Train and support junior team members as appropriate

REQUIREMENTS

  • Bachelor's degree in life sciences or related field, with 3 years’ relevant experience in clinical monitoring or site ID, including demonstrable experience in acting as the main local lead in studies
  • Sound knowledge of medical terminology, GCP, FDA regulations, and Drug Development process and procedures.
  • Strong communication, organizational and interpersonal skills.
  • Proficient in the use of Microsoft Office, Presentation skills and team training.
  • Ability to work independently, prioritize actively, seek input, problem solve and work in a team environment.
  • Strong negotiation skills.
  • Strong verbal and written communication including good command of English language
  • Ability to handle multiple tasks with varying deadlines.
  • Ability to maintain confidentiality.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

Job posted: 2020-06-12

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