Here at Syneos Health we are currently recruiting for a 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.
Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.
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
Qualifications - 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 demonstrated project management experience
- Experience in I-III phase of study execution
- Experience in leading clinical trials and multi-functional teams
- Very good knowledge of GSP/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
#LI-BC1
Disclaimer:
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
Schedule : Full-time
Travel : Yes, 25 % of the Time
Employee Status : Regular