Come discover what our 25,000+ employees already know: work here matters everywhere. We’re a growing and evolving biopharmaceutical industry leader, which means you’ll have endless opportunities to work with experts around the world and build the career you’ve dreamed of.
As a part of the Syneos Health team, you’ll help us deliver results for a rewarding reason – we improve patients’ lives around the world. Because to us, a patient isn’t just a number, they’re our family, friends, and neighbors.
Why Syneos Health
• #SyneosHealthLife means we’re committed to our Total Self culture – where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person’s unique contributions make a difference.
• We believe our success is a direct result of the people who are driving it – you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That’s why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.
We are currently recruiting for a (Senior) Global Project Manager to work on a sponsor-dedicated role for one the world’s leading Pharmaceutical companies located in Switzerland.
The position is office based in Boudry with the possibility of 2 home – based days.
Your main responsibilities:
Leads successful and timely operational execution of global clinical trials from concept to final clinical study report
Focused on project management concepts to support management of issues, risks, timelines and budget
Primary operational contact for the clinical trial
Develop protocol-level documents, plans and training
Collaborate with cross-functional teams and external vendors
Monitor study budget
Contribute to database locks in collaboration with Data Management partners
Manage and comply with various quality and compliance systems
The ideal candidate will need the following experience / skills to be considered:
Bachelor’s or Master’s degree within life sciences or equivalent
Min. 5 years of clinical trial management experience
Experience in leading clinical trials and multi-functional teams
Very good knowledge of GCP/ICH guidelines
Experience with electronic quality, compliance and CTMS systems
Strong organization and time management skills
Ability to effectively manage multiple competing priorities
Fluency in English language
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.
Primary Location: Europe - CHE-Client-Based
Job: Clinical Project Management
Travel: Yes, 25 % of the Time
Employee Status: Regular