Informacje o stanowisku

We are currently recruiting for a Clinical Trial Associate for a global leader in diagnostics/medical industry. This position is responsible for assisting in the execution of clinical trials by providing quality administrative and project management support.

If you already have at least one year of experience in clinical trials and have advanced English skills - this offer is just for you!

Apply and let us know you!

What we expect

• min. 1 year of experience in a clinical research setting
• experience in a healthcare, clinical, or science related field
• Bachelor’s degree in the life sciences or related field
• general knowledge of applicable clinical research principles and requirements, including GCP and ICH guidelines
• fluent English (min. C1)
• proficient in using basic software applications including Microsoft Office and various search engines for conducting Internet searches
• a willingness to learn, and adapt to new processes

Employment agency entry number 47

this job offer is intended for people over 18 years of age

What we offer

• cooperation based on an employment contract
• private medical care
• Multi-Sport Card
• personal insurance plan
• annual bonus
• hybrid work system: 3 days from the office and 2 days of remote work per week
• timeoff to volunteer
• employee recognition platform
• real opportunities to grow your skills in a global setting

Your tasks

• collect essential documents and review for completeness and compliance with Standard Operating Procedures, the protocols, and appropriate regulations
• interact with clinical study sites to support study start-up, execution, and close-out activities
• create and maintain study related trackers, including but not limited to, enrollment, study supplies, receipt of samples, and site information
• coordinate the ordering, tracking, and accountability of clinical supplies
• review for completeness and route legal documents for execution
• draft study documents (study trackers, templates, presentations, etc.)
• support case report form (CRF) development, participate in user acceptance testing (UAT) for electronic data systems and review related data management documents, as applicable
• represent Exact Sciences as a customer advocate/liaison both internally and externally
• coordinate study start-up, execution, and close-out activities, or Investigator Meetings
• identify and report problems, investigate alternatives, and make recommendations for resolution and process improvements
• responsible for organizing cross-functional project meetings
• provide support to Clinical Trial Manager for clinical study budget review, tracking, and maintenance
• author and provide input to Clinical Affairs business processes
• maintain a working understanding of current SOPs, work instructions, applicable regulations, and guidance documents, such as FDA Code of Federal Regulations (CFR) and International Council on Harmonisation (ICH), Guideline for Good Clinical Practices (GCP)

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