Do you want to combine the opportunities that a global company provides with the benefits of a family-owned business? Headquartered in Lachen near Zurich, Switzerland, the Octapharma Group is a leading company in the worldwide market for therapeutic human proteins. Working at Octapharma means to have an opportunity to contribute to our common goal – developing lifesaving therapies to improve patients’ lives.What's the best thing about working with us?You help save lives - Every day is meaningful as we produce life-saving medicinesFamily values - Long-term perspective for employees and relationships Be rewarded with an attractive 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 solutions
What will you be doing as Clinical Trial Manager?Be responsible for the day-to-day operations of clinical trials and the clinical trial implementation in Europe and globally under minimal supervisionContribute to the successful execution of clinical study projectsPerform independent site management of investigative sites, external study vendors and oversight of contractorsParticipate in the development, writing and reviewing of clinical trial documents and manualsParticipate in the feasibility assessments and evaluation of investigative sitesReview and oversee monitoring reportsWho are you?Biological and/or clinical science or nurse/study nurse backgroundMinimum of 3 years experience in clinical research (as CTM) in CRO, pharmaceutical or biotechnology company (monitoring, study management)Proficient In English and GermanStrong operational, presentation, documentation, communication skills, and interpersonal skillsSelf-starter requiring minimal supervision, with a team-oriented approachWilling to travel (approximately 10%)
The Clinical Research and Development Haematology DepartmentThe CRD Haematology Department is part of the CRD department of OctapharmaThe overall responsibility of the CRD Haematology 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 worldwide We primarily work with other internal departments like Regulatory Affairs, Pharmacovigilance, and International Business Units, with external opinion leaders, with study sites and with clinical research organizations.The Haematology team in Lachen, Switzerland consists of 9 people, with further team members and coworkers at locations in Austria and USAYou report to the VP Haematology
Apply Today!Please apply in English. If you have questions about the position, contact Ms. Claudia Vignau, Recruiter; +41 55 451 21 35."The contribution to improving patient care is deeply felt and lived in our day-to-day CRD work, be it through careful planning, acute awareness of the clinical needs, appropriate documentation, or out-of-the-box solutions to unexpected challenges during the study course. This contribution is the actual measure of work satisfaction within the organization and outside of it."- VP CR&D Haematology
If you proceed in the processWe will endeavor to review your profile as quickly as possible and provide you with feedbackThe next step is to conduct a phone interview, which takes about 30 minutes.
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