Home-Based Clinical Research Associate - Clinical Research Coordinator Experience

Job Locations United States
Category
Clinical Operations

Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing approximately 3,500 people across almost 40 countries.

Job Summary

Clinical Research Coordinators wanted at Medpace!  Become a CRA and join our growing team!

 

This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace.  Through our Fast PACE Training Program, you will receive the expedited training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a competitive salary.

 

WE OFFER THE FOLLOWING

  • Competitive travel bonus
  • The opportunity to work from home
  • Retain airline reward miles and hotel reward points
  • Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere
  • In-house travel agents, reimbursement for airline club, TSA pre-check, and automatic enrollment in AAA
  • Opportunity for CRA leadership positions – Lead CRA, CRA Manager
  • Customized Fast PACE training program based on your experience and therapeutic background and interest
  • User friendly CTMS with electronic submission and approval of monitoring visit reports
  • Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
  • Nationwide assignments with average of 2 protocols
  • In-house administrative support for all levels of CRAs
  • Opportunities to work with international team of CRAs
  • Many additional perks unmatched by other CROs!

Responsibilities

 

  • Perform qualification, initiation, monitoring, and closeout visits;
  • Establish an open line of communication with site staff;
  • Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
  • Evaluate the quality and integrity of site practices – escalating quality issues as appropriate;
  • Manage site progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution;
  • Regulatory document review;
  • Medical device and/or investigational product/drug accountability and inventory; and
  • Completion of follow-up activities including visit reports and follow-up letters.

Qualifications

 

  •  Must have a minimum of a bachelor’s degree in a health or science related field;
  • Experience as a Clinical Research Coordinator (minimum 1 year);
  • Approximately 60-80% non-local, nationwide travel is required;
  • Must maintain a valid driver’s license and the ability to drive to monitoring sites;
  • Proficient knowledge of Microsoft® Office;
  • Strong communication and presentation skills; and
  • Must be detail-oriented and efficient in time management.

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 historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
  • Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.

 

EO/AA Employer M/F/Disability/Vets

2020-Top-Cincinnati-Workplace-Ribbon

*WARNING: Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money.  These scammers pose as legitimate employees from actual companies.  Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process.

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