Home-Based Experienced CRA; Clinical Research Associate​/Equity

Position: Home-Based Experienced CRA (Clinical Research Associate)- Bonus/Equity
Job Summary Experienced Clinical Research Associate (CRA) - join our growing team!

Medpace is growing quickly and we are seeking experienced Clinical Research Associates to join our team. We are an innovative, scientifically oriented, mid-sized CRO focused on full-service project work. Through our expedited PACE Training Program, you will receive customized training and efficient onboarding to familiarize yourself with Medpace systems.

We Offer the Following:
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

User friendly CTMS with electronic submission and approval of monitoring visit reports;

Customized, expedited PACE training program based on your experience, therapeutic background, and interest

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

In-house administrative support for all levels of CRAOpportunity 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

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

Qualifications

Clinical Research Associate Experience (minimum 1 year)
Ability to travel 60-70% to locations nationwide is required

Minimum of a bachelor’s degree in a health or science related field

Proficient knowledge of Microsoft Office Strong communication and presentation skills

Detail-oriented and efficient in time management#LI-Remote Medpace Overview 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…