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Job Overview Provide support to the Project Manager and related team members by performing routine procedures and tasks associated with the day to day running of projects throughout the entire study lifecycle (e.g. start-up, maintenance and close-out). Ensure work is conducted in
Essential Functions • Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional development, rewarding and disciplining employees, and addres
The Local Clinical Project Manager (Sponsor dedicated) will be leading Local Study Teams at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines
Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include m
- 根据试验方案、合同规定的工作范围、SOP和GCP的要求进行研究中心筛选、启动、监查和关闭访视。 - 可同时负责多个方案、研究中心和治疗领域内的研究中心监查工作。 - 对所负责的研究中心进行方案和研究相关的培训,与研究中心进行定期沟通以管理项目进行中的要求和问题。 - 评估研究中心工作的质量和完整性,确定研究中心是否是按照方案和适用的法规进行研究。将质量问题汇报给负责的PM和/或直线经理。 - 通过追踪注册申报和批复、招募和入选、病例报告表(CRF)完成和递交、以及数据疑问产生和解决的情况
- Develop basic market research skills / competencies via on-the-job learnings and class-room trainings. - Support project team on overall execution of market research project to ensure timely delivery and assist in proposal preparation. - Assist in drafting research materia
Medical Information Specialist with Greek, German and English This position will put you at the forefront of Patient Safety. With daily direct contact with Health Care Professionals (HCPs) and patients (the very people we are working to help), this is a highly visible and import
IQVIA is hiring Clinical Research Associates (CRA) at the 1 and 2 level. Candidate are required to have 6 months to 2 years of onsite monitoring experience within oncology as well as a preference for Cardiovascular/Renal/Metabolic, and/or Neurology. Candidates can be located anyw
- Ensure the accuracy, completeness, and consistency of data during the production of IQVIA Belgium information assets. - Investigate challenges, analyze complex business problems and make recommendations to improve on data quality and procedures whilst applying best practices -
Vous souhaitez contribuer à améliorer l’accès des patients à des traitements innovants ? Rejoignez-nous en tant que Délégué(e) Hospitalier(ère) dans le Grand Est et contribuez activement au développement des médicaments biosimilaires de nouvelle génération. Véritable partenaire
Job Overview Work performed is in accordance with ICH E6 Guideline for Good Clinical Practice. Essential Functions • Collect all deliveries from loading bay, log, QC, receipt in, store and distribute as required • Maintain stock on shelves in a tidy manner, executing stock rotat
Responsibilities - Work alongside the strategy & investment team of IQVIA’s APAC HQ, supporting routine central planning tasks, strategic initiatives and M&A deal execution; - Help conduct industry research and evaluate potential investment opportunities; - Assist in M&A du
Essential Functions • Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOP
• 作为研究团队成员,遵照法规要求、商定的工作范围、适用的SOP、工作授权和试验方案,在研究中心进行工作。 • 协助研究者完成可行性调查问卷和回收问卷。 • 推动研究中心启动工作:协助研究中心筛选访视,协助及时提交文件到伦理委员会进行审批和试验用药品的发放,协助研究中心启动访视。 • 协助研究者进行受试者筛选和入组研究。 • 得到研究者授权后,根据法规和GCP的要求,协助研究者顺利完成方案要求的随访和步骤:如制定计划、清点核对药品和其他协调工作
工作职责: 1. 作为研究团队成员,遵照法规要求、商定的工作范围、适用的SOP、工作授权和试验方案,在研究中心进行工作。 2.协助研究者完成可行性调查问卷和回收问卷。 3.推动研究中心启动工作:协助研究中心筛选访视,协助及时提交文件到伦理委员会进行审批和试验用药品的发放,协助研究中心启动访视。 4.协助研究者进行受试者筛选和入组研究。 5.得到研究者授权后,根据法规和GCP的要求,协助研究者顺利完成方案要求的随访和步骤:
• Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance and guiding professional development, rewarding and disciplining employees, and addressing employee relati
IQVIA™ – The Human Data Science Company™ – ist ein führender, globaler Anbieter von zukunftsweisender Analytik, Technologielösungen und klinischer Auftragsforschung. IQVIA unterstützt Life Science Unternehmen, Verbände, Institutionen, Kostenträger und weitere Akteure im Gesundhei
IQVIA Health System Services (HSS) wurde 1990 gegründet und ist einer der führenden Technologieanbieter und Dienstleister im deutschen Gesundheitsmarkt. Zu den Schwerpunkten unserer Tätigkeit gehören das Genehmigungs- und Abrechnungsmanagement, die Softwareentwicklung und -bereit
Job Overview IQVIA provides scientific services spanning clinical trials, real world evidence, and consulting in all areas of the product lifecycle. The Patient Centered Solutions (PCS) team leads the industry in generating data to ensure that the patient voice is incorporated i
- 根据试验方案、合同规定的工作范围、SOP和GCP的要求进行研究中心筛选、启动、监查和关闭访视。 - 可同时负责多个方案、研究中心和治疗领域内的研究中心监查工作。 - 对所负责的研究中心进行方案和研究相关的培训,与研究中心进行定期沟通以管理项目进行中的要求和问题。 - 评估研究中心工作的质量和完整性,确定研究中心是否是按照方案和适用的法规进行研究。将质量问题汇报给负责的PM和/或直线经理。 - 通过追踪注册申报和批复、招募和入选、病例报告表(CRF)完成和递交、以及数据疑问产生和解决的情况
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