Clinical Research Associate (Pharm D Candidates)

We are hiring Pharm Ds for the CRA role! 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 rofessionals A chieving C RA E xcellence) Training Program includes the following: A platform to effectively and confidently carry out CRA duties to ultimately become a high-functioning, independent, Medpace CRA Interactive discussions with hands-on exercises and practicums Core departmental rotations to learn various aspects of the drug/device development and approval process Why CRA?

Exciting travel opportunities Make a difference on a larger scale through the development of medical drugs and devices Dynamic working environment with varying day-to-day responsibilities Exposure to multiple therapeutic areas Defined CRA promotion and growth ladder We Offer the Following: CRA training program - PACE® Competitive travel bonus Equity/Stock option program Training completion and retention bonus Annual merit increases 401K matching 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, 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 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 the investigator is enrolling only eligible subjects Regulatory document review <span style="font-family: ar