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 supervision
Contribute to the successful execution of clinical study projects
Perform independent site management of investigative sites, external study vendors and oversight of contractors
Participate in the development, writing and reviewing of clinical trial documents and manuals
Participate in the feasibility assessments and evaluation of investigative sites
Review and oversee monitoring reports
Who are you?
Biological and/or clinical science or nurse/study nurse background
Minimum of 3 years experience in clinical research (as CTM) in CRO, pharmaceutical or biotechnology company (monitoring, study management)
Proficient In English and German
Strong operational, presentation, documentation, communication skills, and interpersonal skills
Self-starter requiring minimal supervision, with a team-oriented approach
Willing to travel (approximately 10%)
The Clinical Research and Development Haematology Department
The CRD Haematology Department is part of the CRD department of Octapharma
The 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 USA
You report to the VP Haematology
What's the best thing about working with us?
You help save lives - Every day is meaningful as we produce life-saving medicines
Family values - Long-term perspective for employees and relationships
Be rewarded with an attractive salary and benefits package
You will have a high level of influence where you can make a difference and leave your footprint
Work with skilled and fun colleagues in a relatively informal organization
Skills development - We offer various internal and external employee and leadership trainings, trainee programs and digital solutions
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 process
We will endeavor to review your profile as quickly as possible and provide you with feedback
The next step is to conduct a phone interview, which takes about 30 minutes.
Would you like to get to know us better? Learn more about us on our website and follow us daily on LinkedIn!
About Octapharma
Headquartered in Lachen, Switzerland, Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines.
Octapharma employs nearly 12,000 people worldwide to support the treatment of patients in 118 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care.
Octapharma has seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany and Sweden, and operates more than 195 plasma donation centres across Europe and the US. Octapharma has 40 years of experience in patient care.
For more information, please visit www.octapharma.com