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Job Details

Clinical Research Associate

Company: Medpace
Location: München (81249)
Reference: 2017-3082
Closing Date: 01 Mar 18
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

Medpace 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 European activities are growing rapidly, and we are currently seeking an office- or home-based CRA/Sr CRA to join our Clinical Operations team. ...

Requirements:

Medpace 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 European activities are growing rapidly, and we are currently seeking an office- or home-based CRA/Sr CRA to join our Clinical Operations team. This position will work on 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.



As a CRA, you will specifically be responsible for the following:

* Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
* Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
* Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
* Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
* Verification that the investigator is enrolling only eligible subjects;
* Regulatory document review;
* Medical device and/or investigational product/drug accountability and inventory;
* Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
* Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement;
* Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.



* Must have a minimum of a university degree in a health or life science related field;
* Min. 2 years of previous experience as a CRA;
* Approximately 60-80% travel in Germany, Austria and Switzerland;
* Proficient knowledge of Microsoft® Office and general computer literacy;
* Outstanding communication and Presentation skills;
* Must be detail-oriented and efficient in time management;
* Excellent verbal and written communication skills in English and German;
* Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities.

AWARDS
Medpace is being recognized locally, nationally, and globally for their work in the industry as well as the culture they have developed for their team.

* Medpace Named a Top Cincinnati Workplace for 2015 by the Cincinnati Enquirer
* Medpace named Top Ten CRO in 2015 CenterWatch Investigative Site Survey
* Medpace once again is nominated for the Eagle Award in 2015 – which recognizes outstanding leadership, professionalism, integrity, and dedication to advancing the clinical research profession through strong site partnerships. (Medpace previous Eagle Award award winner two years running)



WHY MEDPACE?
Join Medpace, a mid-size global CRO that is growing and offers limitless opportunities in career growth and where you will be rewarded for strong performance. At Medpace, you will find work that is both challenging and rewarding and you will be given the tools and training to succeed.



WHAT TO EXPECT NEXT
We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an interview.

Apply for this job: Clinical Research Associate

Contact Information:

Address:  Medpace, Inc
5375 Medpace Way
Cincinnati
Ohio
45227
USA
Tel:  +1 513 579 9911
Fax:  +1 513 579 0444
Website:  Visit Our Web Site

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