Virtual CRC Event - July 23, 2026

Medpace, Inc.•UNAVAILABLE, UNAVAILABLE

17h•Remote

About The Position

Medpace is hosting a Virtual Networking Event to highlight exciting Clinical Research Associate (CRA) opportunities for qualified Clinical Research Coordinators and Research Nurses. This event is an opportunity for clinical research professionals with at least 1.5 years of Clinical Research Coordinator experience to fill CRA openings at Medpace. Through the PACE® Training Program, you will receive the 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.

Requirements

Must have a minimum of a Bachelor’s degree in a health or science related field.
Experience as a Clinical Research Coordinator (minimum 1.5 years).
Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely.
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.
Must be detail-oriented and efficient in time management.

Nice To Haves

Clinical Research Coordinator experience

Responsibilities

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.
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.
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.

Benefits

Competitive travel bonus
Equity/Stock Option program
Training completion and retention bonus
Annual merit increases
401K matching
The opportunity to work from home
Flexible work hours across days within a week
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 and reimbursement for airline club
Opportunity for leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more
CRA training program (PACE®)
Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
In-house administrative support for all levels of CRAs
Opportunities to work with international team of CRAs
Flexible work environment
Competitive PTO packages – starting at 20+ days
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Competitive compensation and benefits package
Structured career paths with opportunities for professional growth
Discounts for local businesses