Project Specialist II

INC Research UK Limited
02 Dec 2017
05 Jan 2018
Contract Type
Full Time
We are currently seeking a Project Specialist to support the contracted services and expectations of clinical studies assigned to our clinical devices project team. This position is located in the UK, Spain or Netherlands at either of our offices.

A brief summary of duties you will be involved in:

* Tracks, processes and analysis clinical information relating to regulatory documents, adverse/serious adverse events, supplies, protocol deviations, IRB approvals, data queries
* Supports the Project Manager with financial aspects such as customer invoices and resource expenses; review of financial reports and analysis of upcoming project events.
* Oversees all regulatory documentation
* Preparation and attendance at Investigator meetings, Kick off meetings, Quick Start Camps and Quality Finish Camps
* Preparation and distribution of all meetings minutes, following up on action points
* Assist with training of new employees to assigned projects

Qualifications This position requires the following skills and experience:

* Degree educated in the science/healthcare field, nursing degree, or equivalent combination of education and experience
* Experience of working in a CRO preferable
* Effective communication and customer interfacing skills
* Basic understanding and knowledge of ongoing protocol and disease related terminology, FDA regulations, GCP/ICH guidelines, drug development process for assigned study, as well as company and sponsor SOPs and WIs
* Strong attention to detail, organizational and problem solving skills
* Ability to perform several tasks simultaneously to meet deadlines
* Self-motivation and ability to work independently

Why choose us:
It takes skill and passion to develop medicines the way we do. Don't worry - if you've got the passion part, we'll help you develop the skills you need to enhance every aspect of your career in the clinical research industry.
We've got an attitude at INC: "Can do, I own it." Absolutely everyone has ownership of what they do here. And because we're given the freedom and responsibility to really own our projects, we can take them to new levels. And that means we can take our careers wherever we want them, too.
"We were ranked "Top CRO" to work with in the CenterWatch 2017 Investigative Site Relationship Survey (a biannual survey of over 2,000 sites worldwide)."

What happens next:
If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.