OverviewBecome part of a vital chain and contribute to our common goal of making people’s lives better. Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation.Join us in shaping our vision to provide new health solutions advancing human life.Clinical Trial AssociateYour main tasks and responsibilitiesSet up and maintenance of Trial Master Files and Investigator Site Files according to Octapharma SOPsAssist the Clinical Team in preparing clinical trial documentsPrepare, distribute, file, and archive clinical documentationReview study files periodically for accuracy and completenessAssist in the organization of Investigator Meetings and participatePerform administrative tasks to support team members with clinical trial execution, as requiredAssists in development of SOPsAssist the Clinical Team in preparation of audits or inspectionsMay act as a central contact for the clinical team for designated project communications, correspondence, and associated documentationManage returning/archiving of study filesAssemble and review regulatory packages for trial-related submissions to RA and IRB/IEC in accordance with ICH-GCP, applicable regulations, company SOPs and check the documents for regulatory submissionsYour expertise and ideal skill setPrevious experience as CTA in international trials or similar experience in office management of international trials would be strongly preferredFluent in both written and spoken English; preferably also in GermanComputer literacyProficient in Word, Excel and PowerPointAble to manage multiple and various tasks with positive attitudeAble to prioritize workload with attention to details and within timelinesWork in a team and independentlyA flexible attitude with respect to work assignmentsYour department - where you make an impactThe Clinical Research and Development (CRD) Lachen team works in the therapeutic areas of Haematology and Critical CareThe overall responsibility of the CRD Lachen department is to develop medicines that target complex and life-threatening conditions.We specialize in clinical development at all stages for newly developed and already marketed productsThe department consists of 11 team members, and you will support both of the therapeutic areas while working in close collaboration with the Business Units, Medical Affairs and Regulatory Affairs.Thrive with usYou help save lives - Every day is meaningful as we produce life-saving medicinesFamily values - Long-term perspective for employees and relationshipsBe rewarded with market-related salary and benefits packageYou will have a high level of influence where you can make a difference and leave your footprintWork with skilled and fun colleagues in a relatively informal organizationSkills development - We offer various internal and external employee and leadership trainings, trainee programs and digital solutionsIt´s in our bloodWe live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion. Please apply in English.Do you have any questions? Then get in touch with your contact person.Mrs. Claudia VignauOctapharma AGSeidenstrasse 2, 8853 LachenT: +41 55 451 21 35Want to find out more about us?Visit our website: Octapharma Career and follow us daily on LinkedIn.About OctapharmaOctapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide.
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