Associate Director, Corporate Quality Partnerships - (15665)

Description

Do you want to work for a global top 10 CRO? INC Research is a full-service clinical research organization, providing the full range of Phase I to IV clinical development services for the world’s pharmaceutical, biotechnology and medical device industries. We do this across six continents. We believe that therapeutic and operational experience forms the foundation for taking medicines successfully through clinical development. From our early days as an academic CNS research organization in the 1980s, to the formation of INC in 1998, to where we are today, we’ve continued to improve what we do.

INC Research was rated the “Top CRO” in the 2013 CenterWatch Global Investigative Site Relationship Survey.

Here at INC Research we value the importance of all departments and their contribution to the success of our work. From Finance to IT, from Recruitment to facilities everyone has the potential to make a difference and ensure our studies run successfully.

As such, due to continued growth, we have an exciting new position for an Associate Director of Corporate Quality Partnerships.

This position can be based in any of our European INC Research Offices.

• A brief summary of duties you will be involved in as an Associate Director of Corporate Quality Partnerships
• To partner with our internal and external customers, providing them with expert support, based on a deep understanding of current global Good Clinical Practice (GCP) requirements and regulatory expectations with the ultimate goal of improved quality and increased customer satisfaction
• To provide strategic Quality oversight for designated key accounts (Sponsor)
• To partner with the designated Account (Sponsor) Management Lead and the customer Quality representative to develop and execute a Quality
• Management Plan that will meet the needs of the customer.
• Continually manage the plan by supporting internal operational teams to ensure quality delivery and continuous improvement.

Qualifications

Thorough knowledge of drug development and ICH GCP Guidelines is necessary
•Experience in Quality Management and/or process improvement is essential
•Comfortable working closely with customers and communicating with Executives
•Highly effective strategic planning, communication, written, presentation and analytical skills
•Advanced proficiency in Microsoft Office Suite (Word, Excel, PowerPoint), email, and voice-mail is required
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.
What happens next:
Once you have submitted your application you will be contacted by one of our dedicated recruiters. If your application is successful they will arrange a suitable date and time to speak to you further about this opportunity.

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract.

Occasionally required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.

Primary Location : Europe - Belgium Regional
Job : Corporate Quality
Schedule : Full-time
Travel : No
Employee Status : Regular