Global Feasibility Associate

Description du poste:

Company Description:

As part of the world's leading testing, inspection and certification company, you share the benefits of our stability and growth; secure employment in a financially stable, Swiss-based company; a proud heritage that has been making the world a better, safer place for over 140 years; and a global, multicultural, and multinational organization.
Grow in a company that is the home of global knowledge and expertise; that operates in a wide range of countries, services and sectors; and that offers you endless opportunities to learn, grow and fulfill you potential!
In the spirit of continued growth, we are currently looking for a Global Feasibility Associate.

Job Description:

The primary responsibility of the Global Feasibility Associate is the organization and coordination of site feasibilities for all multicenter Phase II-IV clinical trial projects.
Your tasks
* Analyse and Assess Request for Proposal
* Review the RFP and the included study description
* Review the protocol for specific information
* Prepare blinded synopsis from protocol summary.
* Draft a feasibility plan in consultation with the Global feasibility manager
* Prepare project-specific feasibility questionnaire
* Prepare message text for the specific project and target population
* Execute Feasibility
* Participate in Kick-off meeting(s)
* Support the development of the feasibility plan
* Identify the persons/sites to be contacted
* Collect Information
* Send out blinded synopsis or feasibility questionnaire to the pre-specified sites
* Follow-up on answers received or outstanding response
* Enter the feedback into the database
* Write Feasibility Outcome Report/ Feasibility Preliminary Assessment
* Draft a feasibility outcome or preliminary assessment report
* Consult with clinical project managers regarding the proposal, including the country split and patient target per country.
* Finalise the report and distribute internally
* Ad hoc requests:
* Assist in preparing PPT slides for bid defense when required
* Identify potential sites for placing trials, assess their interest for close collaboration and conclude with contract.
You will report to Head of Feasibility.

Qualifications:

* University degree (equal to 4 years of college) in (para-)medical, pharmaceutical, sciences, life-sciences or biosciences. Equally recognised degrees and/or relevant qualifications by experience may also be acceptable and assessed on a case-by-case basis.
* A basic to intermediate understanding of clinical trials and key elements of a trial protocol.
* At least 1 year of experience in clinical trial conduct or management (phase I-III) at the site, CRO, or sponsor level would be preferred.
* Knowledge of EU CTR and ICH-GCP and, if applicable, of FDA CFR 21
* Professional: you bring quality, excellence, and ownership to everything you do
* Responsible and results-oriented: you have a sense of accountability for business results
* Committed: you bring your whole self to work with passion and focus
* Driven and eager: you are curious, flexible, and ambitious to learn from a global network
* Open to learning: from the range of different skills, backgrounds, and behaviors around you
* Capable of taking ownership and being independent
* Ambitious: you always challenge yourself to continuously improve and be the best you can be

Additional Information:

What we can offer you:
* A truly rewarding career, working at the highest level of international standards for quality, safety and integrity
* The chance to share our growth and stability.
* Continuous learning from the best experts in the industry
* The chance to expand and enrich your career
* Professional and personal growth
* Experiences and opportunities across the global business

Do you want to be part of this?
Were you already considering a big switch in your career? Maybe this could be your next step. We are looking forward to hearing from you! Send us your story and your resume via the apply button and maybe you will soon join us for work and coffee breaks. Still have questions? Anneleen can give you more details about the job. Send her an e-mail at anneleen.vanbuggenhout@sgs.com