(Senior) Clinical Trial Associate – Sponsor – Dedicated, Czech Republic
Job title: (Senior) Clinical Trial Associate – Sponsor – Dedicated, Czech Republic
Company: Syneos Health
Job description: 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 Clinical Trial Associate role to work for one the world’s leading Pharmaceutical companies located in Czech Republic.
Your main responsibilities:
Providing ongoing administrative support to study team members and other managers
Supporting colleagues in tracking study progress in various studies
Responsible for managing the study documentation (tracking, filing, collecting relevant study information)
Ability to collaborate with Site Staff to resolve daily administrative issues.
Assist study team in coordinating the planning start up, management and monitoring activities.
Responsible for maintaining effective communication and working relationship with internal and external stakeholders
Ability to work effectively in a remote environment
The ideal candidate will need the following experience / skills to be considered:
Min. 1 year on a similar role as a CTA
Good knowledge of country regulations, ICH GCP-guideline
Strong administrative skills
Excellent planning and organizational skills
Ability to manage the multiple priorities simultaneously
Excellent interpersonal, oral, written communication skills
Good level of English (written &verbal communication skills)
Advanced level of Microsoft Office (PowerPoint, Excel, Word & Outlook)
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. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Job date: Fri, 26 Mar 2021 06:16:15 GMT
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