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Clinical Research Monitor(CRA) Milan based (maternity leave replacement)

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Clinical
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18000HZT Requisition #
Thanks for your interest in the Clinical Research Monitor(CRA) Milan based (maternity leave replacement) position. Unfortunately this position has been closed but you can search our 1,357 open jobs by clicking here.

BASIC QUALIFICATIONS:

 

EDUCATION REQUIRED: 

 

Degree in life sciences, nursing or other health related disciplines

 

YEARS OF EXPERIENCE

 

Two (2) years Clinical Research experience

One (1) year of Clinical Research monitoring preferred

 


DESIRED/PREFERRED QUALIFICATIONS

 

Capable of clearly and effectively communicating verbally and in writing

Excellent interpersonal skills

Experience working in a team/matrix environment requiring strong working relationships

Ability to handle and prioritize multiple therapeutic areas and projects simultaneously

Ability to work in a fast paced environment

Competencies and essential skills in the following: cross functional relationships, decision making, execution/results/process improvement, customer satisfaction

Demonstrated ability to maintain composure in difficult circumstances and to identify and adapt to shifting priorities and competing demands

High attention to detail and accuracy

Excellent problem solving skills

Experience with word processing, spreadsheets, and databases applications (e.g., MS Word and Excel)

Basic understanding of any applicable regulations (e.g., Good Clinical Practices, ICH guidelines, FDA CFR, ISO, clinical research ethics, HIPAA and patient privacy laws, EU Directive, etc.)

Business knowledge or experience with the medical / healthcare industry

Class III medical device and/or phase II, III and IV pharmaceutical experience

Experience of conducting clinical research activities in a regulated environment

Proficient knowledge of medical terminology

Regulations/standards training (FDA, ISO, GCP and other country specific training, such as for Canada, Asia, Latin American, etc. as applicable)

Scientific/clinical knowledge needed to adequately monitor the trial (e.g. general therapeutic area education and training)

 

PHYSICAL JOB REQUIREMENTS:

 

The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions

While performing the duties of this job, the employee is regularly required to be independently mobile.  The employee is also required to interact with a computer, and communicate with peers and co-workers

Ability to travel up to 80%

Travel with colleagues and manager as requested.

May require international travel

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