Become 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 Manager - Central MonitoringYour main tasks and responsibilitiesCentral Data ReviewPerform ongoing, in-depth review of clinical trial data across multiple studies (, EDC, IVRS, safety, central laboratory databases).Identify data inconsistencies, missing data, protocol deviations, and outliers at patient and site level.Cross-Study OversightManage simultaneous data review across multiple small trials, ensuring consistency in oversight.Query Management & Data Quality ImprovementReview and initiate targeted queries for critical or inconsistent data points.Provide clear, actionable feedback to avoid repetitive errors.Protocol Compliance MonitoringDetect protocol deviations through data review.Communication & Issue EscalationAct as a central point of contact for data-related issues.Collaboration with Functional TeamsWork closely with:Data Management, Biostatistics, Medical Monitoring, and PharmacovigilanceYour expertise and ideal skill setStrong analytical and clinical judgmentAbility to connect isolated data points across patients and studiesHigh attention to detailEffective prioritization across multiple projectsComfort with manual and semi-structured data reviewYour department - where you make an impactThe overall responsibility of the CRD department is to ensure timely and efficient delivery of clinical study results with a continuous focus on patient safety, on compliance with the clinical research guidelines, codes, rules and regulations, and on delivering the clinical data for improved therapeutic options needed for the care of patients worldwideThe Haematology team is based in Lachen, Switzerland, with further team members and coworkers at locations in Austria and USA You report to the SeniThrive 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 Lachen T: Want 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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