Clinical Project Coordinator

Location:

Maastricht, Limburg, Netherlands

Requisition #:

210000H1

Post Date:

Jan 07, 2021


**Careers that Change Lives**


At Medtronics Bakken Research Center in Maastricht, over 390 experts from more than 33 nationalities work together. They are clinical researchers, scientists and technical engineers who cooperate closely with medical specialists in and outside of Europe to develop new and improve existing therapies in Coronary and Structural Heart (CSH) indications. Our broad range of clinical services includes international clinical trial management, project management, statistical advice, IT support and medical writing.


**A Day in the Life**


In this role, you will be part of the CSH Clinical Research Team.


You will focus on supportive administrative tasks across global or regional clinical studies consistent with applicable regulations, guidelines and policies.


You will prioritize your work to make sure to reach clinical trials milestones and you will communicate about your workload status with your manager and team members on a regular basis.


You will highlight bottlenecks as soon as possible and propose options to your manager to handle them. A straightforward communication is key.


Your main tasks and responsibilities include:


Provide administrative support to study team members within the CSH Clinical Research Team by:


creating and managing the clinical study files and oversees the organization and distribution of clinical study documents


tracking and filing Ethics Committees submissions, case report forms, study reports, and study documentation based on protocol requirements


Provide technical support, which may include data extraction to compile general and cus-tomized reports, data review and tracking


Get a broad practical knowledge of operational systems


Communicate with internal and external contacts


Assists with periodic audits of clinical study files for completeness and accuracy


Make changes in systems and processes to solve problems or improve effectiveness of job area


Assist in the development, implementation and administration of program/system guidelines and procedures


Build experience and become the right hand of the Clinical Research Specialist by for example helping her/him solving open action items, sending out upcoming trending / safety reporting, upcoming compliance emails/scorecards, preparing upcoming payment round and following up on new trainings to be sent out for study team and site personnel


Do you have what it takes:


Bachelors Degree


Strong organization and communication skills


Ability to work in a matrix organization


Fluent in English, both in writing and speaking


Affinity to work with several operational systems


To be successful in this role you recognize yourself as a:


Experience administrative support for Clinical trials


Experience with work prioritization and planning


Experience with work flexibility and teamwork, ready to help team members


**Your Answer**


Is this the position you are waiting for? Dont hesitate and send us your cv and cover letter by using the apply button.
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.