Global Site Staff Training Lead

Recruiter
Syneos Health
Location
London (Greater)
Posted
11 Jan 2018
Closes
10 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Global Site Staff Training Lead

Home based UK or Belgium

Permanent - Fixed term contract.

Here at Syneos Health we are looking for a Global Site Staff Trainer to join one of our sponsor clients.

The Global Site Staff Training Lead is primarily responsible to provide global technical support to the clinical teams in the creation and maintenance of all study customized site staff training documents.mCTMS Trial Builds:

mCTMS Trial Builds:

Monitor the Technical Support eMail Inbox ensuring quick and accurate response to all messages. Create study customized site staff training documents for all new trials. Mentor, liaise and assist GTMs with the development/programming of study customized site staff training materials. Maintain SharePoint site to include all key forms, study training materials and project tracking information. Monitor the Technical Support eMail Inbox ensuring quick and accurate response to all messages.

Create study customized site staff training documents for all new trials. Mentor, liaise and assist GTMs with the development/programming of study customized site staff training materials.

Maintain SharePoint site to include all key forms, study training materials and project tracking information

Updates to existing trials:

Responsible for making protocol required updates to core site staff training forms. Maintain clear versioning for all changes throughout each trial. File all master documents in TMF. Develop communications and tools for GTM/SM/LTM staff regarding the site staff training process. Attend SMT meetings and other study team meetings as required. Provide supplemental training/support to GTM/LTM/SM roles. Liaise with GTMs to assess and apply protocol required changes master.

A minimum of a Bachelor's/University degree or equivalent experience is required. A minimum of 5 years clinical trial experience in the pharmaceutical and/or health care industry is required. Knowledge of required clinical trial documentation and operational experience in clinical trials with a pharmaceutical company and/or a CRO is required. The individual must work well in an international environment. The individual should be able to handle multiple projects simultaneously and have excellent project management and organizational skills. Excellent communication skills (written and verbal English) are required. High level of technical knowledge in Excel and WORD is required. Must have extreme attention to detail; Ability to work under tight timelines and be accurate; Strong communication and training skills.

Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.