(Snr) Global Trial Manager

Job content

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 several (Snr) Global Trial Manager/PMsto work on a sponsor-dedicated role for one the world’s leading Pharmaceutical companies located in Switzerland.

The position is 50% office based in Boudry, with the rest of the work week being home-based.

The level of the role will be adjusted to the successful candidates´ experience, however below are some sample responsibilities and qualifications.

Your Main Responsibilities

• Lead successful and timely operational execution of global insourced or outsourced, non-registrational data generating or registrational data generating interventional clinical trials from concept to final clinical study report
• Act as the primary operational contact for the study and leads the cross- functional global team for execution of the study
• May provide quality oversight of one or more Contract Research Organization (CRO) teams and vendors.
• Focus on project management concepts to support management of issues, risks, timelines, and budget and ensure quality compliance with ICH/GCP, Regulatory Authorities’ regulations/guidelines, and applicable SOPs/WPs
• Act as the primary operational contact for the clinical trial
• Develop protocol-level documents, plans and training
• Collaborate with cross-functional teams and external vendors
• Contribute to database locks in collaboration with Data Management partners
• Manage and comply with various quality and compliance systems
  

Qualifications

• Minimum of BA/BS or equivalent in relevant discipline, and fluency in English
• Min 2 yrs (the more you have the role will be adjusted to your level) experience of demonstrated project management experience
• Experience in leading global clinical trials and multi-functional teams
• Experience in, ideally, all phases of study execution, and thorough knowledge of GCP/ICH guidelines/regs
• Demonstrated singular leadership of a global clinical trial/significant geographical portion of trial/ISR/cross RDG and NRDG/other applicable Pharma experience
• Demonstrated project management and organizational skills with strong presentation and communication abilities
• Experience with electronic quality, compliance and CTMS systems
• Knowledge of pharmaceutical industry regarding pre-clinical, clinical, regulatory and commercial components - focus on clinical components
• Ability to travel for work, estimated at ≤ 25%
  

Nice To Have

• TA experience in Oncology, CV, Immunology, Fibrosis, Neuroscience, Clin Pharm
• Experience managing CROs
• Risk Management experience preferred
  

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