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Join to apply for the Senior Clinical Project Manager role at Octapharma
Job-ID: 60004
Location: Lachen, CHE
Job Level: Professionals
Category: Research and Development
Employment Type: Permanent position
Would you like to combine the opportunities provided by a global company 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 having 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 medicines
Family values - Long-term perspective for employees and relationships
Be rewarded with market-related 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
What will you be doing as Senior Clinical Project Manager?
Planning, implementation and evaluation of global clinical Phase 1-4 GCP studies
Directing activities of team members to ensure compliance with protocols and overall clinical objectives. Providing input to overall clinical development programs with coagulation and critical care products and lead the development of study protocols
Evaluate, analyse and interpret clinical data. Preparing study reports, CTDs, summary reports, expert statements, etc. for Competent Authorities
Keeping track of study budgets, involvement in vendor oversight
Interacting with Independent Data Monitoring and Steering Committees (install, update, present results, etc.)
Representing Octapharma`s Clinical Research at meetings with Competent Authorities
Contribute to publications and prepare abstracts, posters and/or presentations for national and international congresses
Review scientific literature, participate in continuing education activities or attend conferences and seminars to maintain / keep up to date current knowledge of all aspects regarding clinical studies
Who are you?
PhD or MD background
Minimum of 8 / 13 years experience in clinical research (as CPM / 10 years for Senior CPM) in a pharmaceutical or biotechnology company
Excellent communication skills to be able to effectively convey messages across to both study team members and other external persons like vendors and external consultants
Good organizational, and leadership skills
Ability to maintain oversight of various aspects of the clinical study conduct and to integrate cross-functional input into development milestones
Ability to pay keen attention to detail at all times and work within stipulated timeframes or deadlines even in the face of multiple responsibilities or projects
Engaging and convincing personality for team building and in many cases leading a team
In depth knowledge of medical terminology, physiology and pathophysiology related to the relevant clinical trial
Experience in writing clinical study procedures and other clinical documents
Preferably experienced in the field of coagulation and critical care
Excellent problem-solving skills with ability to daily resolve trial issues
Strong project management skills and planning competencies to set plans and execute on time and within budget
Experience managing CROs and outside vendors to plan and execute Phase 1- 4 clinical trials
Excellent presentation skills and expertise in stakeholder management
Demonstrated ability to collaborate, multi-task and work effectively in a fast-paced matrix environment
Fluent in German and English (written and spoken)
Willing to travel up to 30%
Apply Today!
If you have questions about the position, contact Ms. Claudia Vignau, Senior Expert Talent & Acquisition; +41 55 451 21 35
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
Octapharma 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.
For more information, please visit www.octapharma.com
Apply now
Seniority level Seniority level Mid-Senior level
Employment type Employment type Full-time
Job function Job function Project Management and Information Technology
Industries Pharmaceutical Manufacturing
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