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.

Here at Syneos Health we are currently recruiting for a (Senior) Clinical Trial Associate in Boudry (Switzerland) for an office - based sponsor-dedicated role with the possibility of 2 home-based days.

Your main responsibilities:

Contributes to the operational execution of clinical studies, e-filling the documents including QC and follow up with the team

Reviews of invoices

Collaborates closely with the global team members

Provides operational input on development, management and maintenance of study deliverables

Drives process/system enhancements related to role responsibilities

Manages various quality and compliance systems

Uses applications and software to support the processes and team

Attend global meetings and contribute meeting minutesThe ideal candidate will need the following experience / skills to be considered:

Min. 1 year of experience on a similar role

Good knowledge of CTMS and eTMF

Excellent communication, prioritization, organizational and time management skills

Proficient use of Microsoft Office and general computer systems

Fluency in English language (both written and spoken)

#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.