Senior / Regional Feasibility Specialist and Site Identification (Base in any South-East Asia countr Job in Tanjong Pagar, Central Business District Singapore
Quintiles pioneered the idea of helping pharma companies conduct objective clinical trials to establish not only whether a drug is effective, but who can take it safely. Our customers have relied on us to design and conduct rigorous clinical research for decades, from small studies to multinational mega-trials. However, we continue to develop new ways of interpreting and evaluating data that allow us to create more effective trials and determine outcomes faster. If that is your passion, we have a place for you.
We are looking for suitable individuals to fill the position of :
Senior / Regional Feasibility Specialist and Site Identification (Base in any South-East Asia countries)
Job Responsibilities
• Accountable for making recommendations for Quintiles commitments for future studies in terms of recruitment rate, timelines and screen failure rates
• Take independent responsibility for capability exercises and larger feasibility projects / deliverables
• Prepare for strategy calls by research into therapeutic areas using internal databases, scientific literature, the
internet and expert medical knowledge to provide background information.
• Attend strategy calls with internal stakeholders including Medical Directors and Advisors, Business Developers,Sales Staff and Program Directors. Present background information, particularly including country recruitment and screen failure data.
• Design of protocol-specific questionnaires for collection of global feasibility information for individual countries and sites in order to determine patient populations and protocol suitability.
• Develop feasibility analysis systems and data collection tools in Excel to support the collection of associated metrics
• Provide appropriate tools for country feasibility leads to carry out feasibility and capability exercises e.g. telephone training and detailed emails
• Coordinate the collection and analysis of global feasibility information to meet the challenging timelines of the proposal process and independent feasibility assessments
• Reconcile and interpret feasibility data, providing solid recommendations to internal stakeholders
• Production of feasibility text for proposals and feasibility reports
• Review budgets for stand-alone paid feasibility studies
• Train and support new team members
• Attend client meetings as required to present feasibility process and explain recommendations
• Liaise with internal and external customers globally to coordinate the collection and delivery of feasibility data.
• Maintain and update departmental information repositories and databases
Requirements:
• Degree in Science, with a major in Pharmacy, Biological / Life Sciences or Nursing from a recognised tertiary institution.
• Minimum 1 year relevant experience in the pharmaceutical / CRO industry
• Good knowledge of drug development process, clinical trial monitoring procedures, GCP guidelines and medical terminology.
• Excellent analytical and problem-solving skills.
• Effective organizational, verbal/written communication and interpersonal skills.
• Able to travel when required.
• Can be based in any of South-East Asia (Singapore/Malaysia/South Korea/Taiwan/China)
