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Job Details

CRA Denmark

Company: RBW Consulting
Location:
Reference: CRA-dk
Closing Date: 16 Dec 16
Type: Full Time
Salary (£): Competitive
Benefits:

Job Summary:

CRO is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team!

Requirements:

Description

SUMMARY OF POSITION

 

CRO is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team!

Our clinical activities are growing rapidly, and we are currently seeking a full-time, home-based Clinical Research Associate to join our Clinical Operations team. This position will work with a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

The Clinical Research Associate at CRO is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivalled support to our customers. If you want an exciting career where you use your medical or health background and education, travel extensively and are instrumental in the clinical trials process, this could be the opportunity for you. Our successful Clinical Research Associates possess varied backgrounds in the medical and related healthcare fields. Individuals who have succeeded in the CRA role include Registered Nurses, Dieticians, Pharmacy Technicians, Pharmaceutical Sales Representatives and Research Assistants. An extensive training program provides the platform to effectively and confidently carry out your duties. 

DESCRIPTION OF JOB DUTIES
•Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
•Perform source document verification and case report form review;
•Perform regulatory document review;
•Conduct study drug inventory;
•Perform adverse event and serious adverse event reporting and follow-up; and
•Assess patient recruitment and retention.

 

QUALIFICATIONS/REQUIREMENTS:
•Bachelor of Science in health-related field;
•Broad knowledge of medical terminology and clinical patient management;
•Basic knowledge of drug therapy techniques and clinical research methodologies;
•Broad knowledge of the local language and excellent English.
•Clinical research experience.

If you are interested in this position then please contact Nathalie Nordqvist at RBW Consulting using the email address or link provided on this website. 

 

Apply for this job: CRA Denmark

Contact Information:

Address:  Brighton
Southdown House, 130a Western Road, Brighton BN1 2LA
BN1 2LA
England
Tel:  01293 584 300

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