Junior Clinical Project Manager - Germany - International Development Nr ref.: /JOBS.pl My client is looking for experienced CRA II's / SCRAs to join their company as Junior Project Managers! During this period of exciting growth they have tasked me to find some of the best SCRA's looking to progress their career. Due to several business wins, my client is looking to expand their clinical teams across the business. These are home and office based roles that are available. I am looking for candidates who have proven independent, multi-centric monitoring experience. About the opportunities. Depending on experience responsibilities include: All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties All aspects of site and registry management as prescribed in the project plans Organize and make presentations at Investigator Meetings Report, write narratives and follow-up on serious adverse events Review progress of projects and initiate appropriate actions to achieve target objectives You may serve as lead monitor for a protocol or project and assist in establishing monitoring plans if required Participate in the development of protocols and Case Report Forms as assigned Interact with internal work groups to evaluate needs, resources and timelines Education/Qualifications Typically required: University/college degree (life science preferred), or certification in a related allied health profession (e.g. nursing certification, medical or laboratory technology). Alternatively, candidates with two or more years of relevant clinical research experience in pharmaceutical or CRO industries will also be considered Experience Typically required: Clinical research monitoring experience (including pre-study, initiation, routine monitoring and close-out visits) preferably in a CRO or Pharma environment Ability to monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP and ICH Guidelines Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs Good knowledge of ICH Guidelines and GCP, monitoring procedures and understanding of the clinical trial process Good planning, organization and problem solving abilities Good communication and interpersonal skills This role offers a very clear career progression with amazing training schemes in place to get you to fast track your clinical career! With an amazing culture and family feel this company is renowned for their work atmosphere and has been voted one of the best companies to work for in 2015 & 2016! Act now and apply If you feel you would be the right person for this job or know anyone who you believe this would be ideal for please contact me on or email me on Clinical Trials / Clinical Research / SCRA / RGN / Clinical Research Organisation / CRO / Research Services / Pharmaceutical industry / CRO's / Phase I / Phase II / Phase III / Phase IV / Oncology / Cardiovascular / Therapy Areas / Home based / Office Based / Development / Culture / Progression / Competitive Salary / Sunny / Job Satisfaction / Neurology / Rare Diseases / Pharma Market / Global Exposure Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .
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