Clinical Research Monitoring (CRA)

The Clinical Research Associate position offers an exciting career within clinical research! For those with Pharm D backgrounds wanting to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this is the right opportunity for you!

This position is office based in Cincinnati, OH.

Medpace CRA Training Program (PACE®)

No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. The PACE® (P A C E) Training Program includes the following:

A platform to effectively and confidently carry out CRA duties to ultimately become a high-functioning, independent, Medpace CRA

Exciting travel opportunities

Make a difference on a larger scale through the development of medical drugs and devices

CRA training program - PACE®

Competitive travel bonus

Equity/Stock option program

Training completion and retention bonus

Opportunity to work from home

Flexible work hours across days within a week

Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere

In‑house travel agents, reimbursement for airline club membership, and TSA pre‑check

Opportunity for leadership positions - Lead CRA, CRA Manager, Training and Development Manager, and many more

Ongoing therapeutic training by our in‑house physicians who are medical and regulatory experts

In‑house administrative support for all levels of CRA

Opportunity to work with international team of CRAs

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol

Communication with the medical site staff including coordinators, clinical research physicians, and their site staff

Verify 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

On‑site and virtual/remote monitoring activities with a risk‑based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward

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

Assess 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

Minimum of a Bachelor’s degree in a health or science related field; Ability to travel 60-70% to locations nationwide is required

Proficient knowledge of Microsoft Office

Medpace is a full-service clinical contract research organization (CRO) providing phase l‑lV 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 the advancement of clinical research. We leverage in‑country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti‑viral and anti‑infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

When you join Medpace, you become part of an innovative team that brings cutting‑edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross‑functional collaboration.

Work alongside physicians, scientists, and industry‑leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.

Continuous Growth & Development

Office based environment with on‑site mentors

Industry renowned onboarding and training programs designed to accelerate professional development

Ongoing training and continuous learning opportunities throughout your career

Competitive compensation programs that recognize and reward performance

Comprehensive health, wellness, retirement, and PTO benefits

Office based culture with occasional WFH that provides flexibility for eligible positions after training

Multiple on‑site dining options in the heart of Madison Square

Free on‑site parking

Convenient access to on‑site 24‑7 fitness and wellness facilities

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

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