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Clinical Research Monitor


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  • Biotechnology / Science
  • Healthcare
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Job Details

Company Medtronic
Job Title Clinical Research Monitor
JobId 27058
Location: Budapest, HUN

Clinical Research Monitor


Budapest, Budapest, Hungary

Requisition #:


Post Date:

Nov 29, 2017

**Clinical Research Monitor** **– Budapest, Hungary.**

**Careers that Change Lives**

Would you like to work for a rapidly growing international healthcare

Do you consider you have the right experience for a Clinical Research Monitor role? If yes, then send us
your resume and enter the recruitment process right away!

Join Medtronic where we appreciate your talent,
experience and passion for your work. You can count on professional and
personal development, exciting challenges and a dynamic environment.

This is an exciting opportunity where, as a Clinical
Research Monitor youwill be
responsible for the oversight of clinical research, conducted at
investigation sites to ensure compliance with study protocols, applicable
regulatory standards, IRB/EC policies and procedures and business

In return, we will provide you with world-class
training, development opportunities, and the opportunity to work in a varied
and challenging role. Our offer package will include a competitive salary and
other great benefits.

For this role
you will be expected to be located in Budapest, Hungary.

**A Day in the Life**

**Principal responsibilitiesof Clinical Research Monitor:**

+ Perform sitemonitoring visits in accordance with the study Monitoring Plan to ensurecompliance with the Investigational Plan, Monitoring Plan, applicable regulatory,IRB/EC, and Medtronic standards, guidelines and policies.

+ Prepare sitevisit reports and correspondence for all visits conducted in accordance withthe study Monitoring Plan.

+ Communicatevisit findings with site personnel, ensure relevant follow-up.

+ Identificationand escalation of protocol deviations, discrepancies in data, andnon-compliance to study protocols, applicable regulations, Good ClinicalPractices and Standard Operating Procedures.

+ Identify siteneeds, provide solutions to facilitate the clinical trial process.

+ Act as a primarypoint of contact for study sites as requested.

+ Assist ininitial and ongoing site personnel training as required.

+ Possess aworking knowledge of disease state and investigation product.

+ Attend Investigatorand/or Coordinator meetings.

+ Lead allrelevant monitor responsibilities.

**Must Haves and Nice to Haves**

+ Bachelor’s Degree in life sciences, nursing or otherhealth related disciplines.

+ Min. 2 years of Clinical Research experience.

+ Proficient knowledge of medical terminology.

+ Clear and effective communication skills.

+ Excellent interpersonal skills.

+ Experience working in a team/matrix environmentrequiring strong working relationships.

+ Ability to handle and prioritize multiple therapeuticareas and projects simultaneously.

+ Ability to work in a fast paced environment.

+ High attention to detail and accuracy.

+ Excellent problem solving skills.

+ Computer literacy (MS Word, Excel, PP).

+ Ability to travel up to 80% (may require alsointernational travel).


Is this the position you were waiting for? Then
please apply directly via the apply button!

**About Medtronic**

Together, we can change
healthcare worldwide. At Medtronic, we push the limits of what technology, therapies and services can
do to help alleviate pain, restore health and extend life.

We challenge ourselves and each other to make tomorrow better than
yesterday. It is what makes this an exciting and rewarding place to be.

We want to accelerate and advance our ability to create meaningful
innovations - but we will only succeed with the right people on our team.

your specialty or ambitions, you can make a difference at Medtronic - both in
the lives of others and your career. Join us in our commitment to take
healthcare Further, Together.

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