London - Clinical Trial Assistant (Site Budget & Contracts)

placeLondon calendar_month 
Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Assistant to join our Clinical Operations team. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success.

If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities
  • Finalization and quality check of contracts, amendments and other contract related documents before they are sent for signatures (EMEA, APAC);
  • Uploading fully executed legal documents to the Company’s data bases;
  • Performing Quality Checks of contracts, amendments and other contract related documents uploaded to the Company’s data bases( EMEA and APAC). Active participation in resolving any discrepancies or quality issues if detected;
  • Support for APAC, EMEA Contract Team (shipment of documents, tracking progress of signatures, following up on the status of documents etc.), if required;
  • Tracking progress of assigned tasks in the Company’s tracking systems.
Qualifications
  • A high school diploma or equivalent (Bachelor’s degree preferred);
  • Proficiency English;
  • At least 1 year of CTA experience would be ideal;
  • Excellent organizational and prioritization skills;
  • Knowledge of Microsoft Office programs; and
  • Attention to detail and excellent oral and written communication skills.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.

We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 4,000 people across almost 40 countries.

Why Medpace?

When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.

Awards:

  • Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
  • Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.

Medpace Perks
  • Competitive PTO packages
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Flexible work schedule
  • Competitive compensation and benefits package
  • Structured career paths with opportunities for professional growth
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