久久久久久久久免费_久久久久久久久网站_久久久久久久久一区_久久久久久久网_一级免费在线_一级女人真人毛片免费看

工作职责:Why Patients Need YouPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.What You Will AchieveYou will facilitate in conducting clinical trials and monitoring their progress. You will coordinate all activities that support the clinical trials and assist the managers in conducting them. As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team.? Your focus and ability to meet team targets will help in completing critical deliverables.It is your hard work and commitment that will help in making Pfizer ready to achieve new milestones and help patients across the globe.How You Will Achieve ItContribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.Identify issues that may impact on the conduct of the study and ensure appropriate closure of all issues.Assist Clinical Research Site Assistant in site activation activities such as gathering IIP documentation where required to ensure timely site activation.Reviews data to ensure quality and completeness, including Quality Control (QC) review of documents.Ensure clinical trials data are submitted to data management in a timely fashion.Support the study clinician in ensuring patient safety and eligibility.Ensure induction and appropriate Pfizer specific trainings are undertaken.Provide support for coordinating with sites for finalizing budget worksheets and contractual agreements.Maintain accurate site-level information on corporate clinical trials registry.Support study team as needed with Regulatory, Central, and Local Ethics Submissions and responses.Ensure patient safety is maintained and all safety issues are reported correctly according to all relevant local and international regulatory requirements.Maintenance of Electronic Library and Records Archive etc. to ensure audit trail is complete and accurate.Attend investigator meeting when required.??任职资格:QualificationsMust-HaveBachelors Degree3 years CRA experienceExperience in clinical trial administration and clinical trial monitoringDemonstrated success/results in prior roles including matrix organizationDemonstrated knowledge of quality and regulatory requirements across a range of different countriesKnowledge of International Conference on Harmonization Good Clinical Practices and local regulationsKnowledge of applications used in the clinical trialsSOP compliance knowledge and expertise on all relevant SOPsEffective verbal and written communication skills, and must be fluent in EnglishProficiency in Microsoft SharePoint, SharePoint Designer etcNice-to-HaveMasters degreeRelevant therapeutic area experienceHigh level of project management skills#LI-PF 职能类别：医药技术研发人员