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Clinical Research Associate - Research Nurses

Company

Medpace, Inc.

Address , Cincinnati, 45227, Oh
Employment type FULL_TIME
Salary
Expires 2023-06-29
Posted at 1 year ago
Job Description
Job Summary:
We are hiring Nurses at Medpace!

The Clinical Research Associate position at Medpace offers 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 a Research Nursing background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

Positions are office based in Cincinnati-OH and Dallas-TX


MEDPACE CRA TRAINING PROGRAM (
PACE®)

No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE®. 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.

WHY BECOME A CRA

This role takes you on a journey through travel and excitement which 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:

  • Expansive experience in multiple therapeutic areas
  • Competitive pay and many additional perks unmatched by other CROs (SEE BELOW).
  • Work within a team of therapeutic and regulatory experts
  • Dynamic working environment, with varying responsibilities day-to-day
  • Defined CRA promotion and growth ladder with potential for mentoring and management advancements


WE OFFER THE FOLLOWING

  • Training completion and retention bonus;
  • Flexible work hours across days within a week;
  • Annual merit increases;
  • Equity/Stock Option program;
  • The opportunity to work from home;
  • Opportunities to work with international team of CRAs.
  • CRA training program (PACE®);
  • Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts;
  • In-house travel agents, reimbursement for airline club, TSA pre-check, and automatic enrollment in AAA;
  • Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere;
  • Retain airline reward miles and hotel reward points;
  • Opportunity for leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more;
  • Competitive travel bonus;
  • 401K matching;
  • In-house administrative support for all levels of CRAs; and
Responsibilities :
  • Verification that the investigator is enrolling only eligible subjects;
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
  • Communication with the medical site staff including coordinators, clinical research physicians, and their site 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;
  • Medical device and/or investigational product/drug accountability and inventory;
  • Regulatory document review;
  • Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
  • Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
  • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
Qualifications :
  • Must have a minimum of a Bachelor’s degree in a health or science related field; BSN preferred
  • Must maintain a valid driver’s license and the ability to drive to monitoring sites;
  • Minimum 1 year healthcare-related work experience preferred;
  • Must be detail-oriented and efficient in time management.
  • Proficient knowledge of Microsoft® Office;
  • Strong communication and presentation skills; and
  • Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits required;

Medpace 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 more than 5,000 people across 40+ countries.
Why Medpace?:
People. Purpose. Passion. Make a Difference Tomorrow. Join Today

The work we’ve done over the past 30 years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Celebrates 30 Years
As we celebrate 3 decades of industry expertise and organic growth, we recognize the global team responsible for driving clinical development at Medpace. Click here to learn more about Medpace Celebrating 30 Years.
Cincinnati Perks
  • Flexible work hours
  • Hybrid work-from-home options (dependent upon position and level)
  • Community involvement with local nonprofit organizations
  • Discounted tuition for UC online programs
  • Partnership and discount with onsite childcare
  • Structured career paths with opportunities for professional growth
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Official Sponsor of FC Cincinnati
  • Modern, ecofriendly campus with an on-site fitness center, bar, and restaurants
  • Cincinnati Campus Overview
  • Employee health and wellness initiatives
  • Discounts on local sports games, local fitness gyms and attractions
    • Official Sponsor of FC Cincinnati
  • Company-sponsored employee appreciation events

Awards:
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
  • Recognized by Forbes as one of America's Best Mid-size Companies in 2021 and 2022

What to Expect Next:
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

EO/AA Employer M/F/Disability/Vets