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Job Details

Junior Clinical Research Associate

Company: Medpace
Location:
Reference: DEJCRA1118
Closing Date: 23 Dec 18
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

Medpace is looking for a Junior CRA to join our Clinical Monitoring team in Munich, Germany

Requirements:

Junior Clinical Research Associate

Location: Munich, Germany 

Overview

Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,700 people across 36 countries.

Job Summary

The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development. 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. 

 

PACE – MEDPACE CRA TRAINING PROGRAM

No clinical experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.  Through ourPACE Training Program, you will join other  Professionals Achieving CRA Excellence:

  • PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.
  • PACE will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.
  • To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process. 

UNEXPECTED REWARDS

This role will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices.  The CRA position provides many other distinctive advantages including:

  • Dynamic working environment, with varying responsibilities day-to day;
  • Expansive experience in multiple therapeutic areas;
  • Work within a team of therapeutic and regulatory experts;
  • Defined CRA promotion and growth ladder with potential for mentoring and management advancements;
  • Competitive pay and opportunity for significant travel bonus.

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; and
  • 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

  • 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; and
  • Excellent verbal and written communication skills in English and German.

Why Medpace?

When you join Medpace, you become part of a team dedicated to supporting the development of ground breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities. 

 

Awards

  • Medpace Named a Top Cincinnati Workplace for 2015, 2016, 2017 and 2018 by the Cincinnati Enquirer
  • Winner of the ACRP-Avoca CRO Quality Award in 2018
  • Recognized with six CRO Leadership Awards from Life Science Leader magazine
  • Eagle Award winner - which recognizes outstanding leadership, professionalism, integrity, and dedication to advancing the clinical research profession through strong site partnerships

 

What to Expect Next

We look forward to receiving your application (CV and cover letter).  A member of our recruitment team will review your qualifications and if interested, you will be contacted for an interview.

 

Apply for this job: Junior Clinical Research Associate

Contact Information:

Address:  Medpace Germany GmbH
Theresienhoehe 30 80339 München Germany
80339
Germany
Tel:  +49 (0) 89 89 55 718 0
Website:  Visit Our Web Site

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