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Job Details

Senior Clinical Research Associate

Company: Medpace
Location: München (81249)
Reference: 2016-2156
Closing Date: 22 Dec 16
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

The Clinical Research Associate position at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. ...

Requirements:

The Clinical Research Associate position at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and/or health/life science interest and background who want to explore the research field, travel throughout Germany, Austria, Switzerland, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. Individuals who have succeeded in the CRA role include:
•Dieticians
•Pharmacists
•Pharmaceutical/Device Sales Representatives
•Biotech Engineers
•PhD/Pharm.D candidates
•Health and Wellness Coordinators
•Research Assistants.



JOB DUTIES AND MAIN RESPONSIBILITIES
As a CRA, you will specifically be responsible for the following:
•Conduction of 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.



QUALIFICATIONS/REQUIREMENTS:
•Must have a minimum of a university degree in a health or life science related field,
•Approximately 60-80% travel;
•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;
•Previous experience as a CRA of min. 2 years as well as
•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: Senior 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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