Global Clinical Research Associate Opportunities

Global Clinical Research Associate Opportunities

Responsibilities 

SUMMARY OF POSITION

Our European 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 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.

Ours is a culture of expertise, and we empower our teams to employ their unique talents and experience to take an assertive approach to research, problem solving, and ultimately supporting our partners. At Medpace our employees embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return they are rewarded with interesting projects, career advancement, and recognition and exposure to our international footprint. These are just a few reasons talented individuals join the Medpace team.

The Clinical Research Associate at Medpace is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivaled 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.

 DUTIES AND MAIN RESPONSIBILITIES

•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.
•At least 2 years of proven track record of monitoring experience.

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.

EO/AA Employer M/F/Disability/Vets

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