This home-based opportunity is for clinical research professionals with at least two years of Clinical Research Coordinator experience to become Clinical Research Associates (CRA) with Medpace. Through the PACE® Training Program, you will receive the necessary training to become a fully resourced CRA. You will also have the opportunity to earn a generous travel bonus.
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
Communicate with 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
Perform medical record and research source documentation verification against case report form data, including informing site staff of any entry errors, ensuring good documentation practices are adhered to, and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
Conduct on-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through the 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
Verify the investigator is enrolling only eligible subjects
Review regulatory documents
Perform medical device and/or investigational product/drug accountability and inventory
Verify and review 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 offer suggestions for improvement
Complete monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance
Requirements
Minimum of a Bachelor’s degree in a health or science related field
Experience as a Clinical Research Coordinator (minimum 2 years)
Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely
A valid driver’s license and the ability to drive to monitoring sites
Proficient knowledge of Microsoft Office
Strong communication and presentation skills
Detail-oriented and efficient in time management
Benefits
Competitive travel bonus
Equity/Stock option program
Training completion and retention bonus
Millions of jobs, with real people getting hired every day
200,000+
New jobs added daily
7,000,000+
Verified job listings
1,000,000+
Tailored applications submitted
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
CRA training program - PACE®
Ongoing therapeutic training by in-house physicians who are medical and regulatory experts
In-house administrative support for all levels of CRA
Opportunity to work with an international team of CRAs
Purpose-driven work alongside physicians, scientists, and industry-leading experts
Collaborative culture with an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust
Accessible and approachable leadership
Office-based environment with on-site mentors
Defined career paths with clear advancement opportunities
Industry-renowned onboarding and training programs designed to accelerate professional development
Ongoing training and continuous learning opportunities
An environment that encourages employees to influence change, contribute ideas, and grow quickly
Comprehensive health, wellness, retirement, and PTO benefits
Office-based culture with occasional WFH that provides flexibility for eligible positions after training
Company-sponsored social events and intramural sports
A modern corporate campus designed to support collaboration and productivity
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
Application Process
A Medpace team member will review your application
If your profile matches current needs, you will be contacted for an interview
About the Company
Medpace is a full-service clinical contract research organization (CRO) providing phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Its mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. Medpace leverages 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, it employs more than 6,500 people across 40+ countries.
