R&D Clinical Trial Manager

Location: Belgium

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Pharmaceutical organization, based in Belgium.

The company is a big international player with multiple locations throughout the world. This office is based in Diegem, just above Brussels.

ROLE DESCRIPTION

As a local Trial Manager you are responsible for leading one or several clinical trials to execute company sponsored clinical trials for the medical devices franchise.

You have to work 3 days a week in the Diegem office, 2 days can be home based. The position is for 40 hours a week and the contract for at least one year.

RESPONSIBILITIES

• Serve as a Clinical Trials Leader within the Clinical R&D Operations CoE operations group to execute company sponsored clinical trials for the Medical Device Franchises
• Manage all operational activities of assigned clinical studies within the Clinical R&D Operations group
• Serves as a member of the clinical trial/study/program core team and may serve as the liaison with the Clinical R&D Franchise and Clinical R&D BSDM for projects under his/her responsibility
• May serve as the primary contact for clinical trial sites
• Independently solves problems arising during clinical study execution, and will seek guidance for more complex problems, as needed
• Provide internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders
• May be involved in other tasks to support Clinical R&D Operations and R&D Clinical Franchise as needed
• Plan, track, and manage assigned clinical trials/programs budgets to ensure adherence to business plans
• Support the implementation of new clinical systems/processes, and provide support for publications, as needed.
• Interface and collaborate with site personnel, IRBs/ECs, Competent Authorities/MoH, contractors/vendors, and company personnel
• Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliance
• Manage resources assigned to designated clinical studies to provide quality deliverables while maintaining optimal efficiency

REQUIREMENTS

- 4 years experience in clinical research
- Knowledge of GCP
- Experience with Project Management
- Experience with clinical Trials
- Advanced Technical Writing Skills
- Fluent in English
- Dutch
- Plus: (not required) medical device experience
- Pus: (not required) experience managing others

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Romy van Ooijen.