Bachelor's degree in health or science related field
Minimum 2 years experience as a Clinical Research Coordinator
Willingness to travel 60-70% nationally
Valid driver's license for travel to monitoring sites
Proficient in Microsoft Office suite
Strong communication and presentation skills
Detail-oriented with effective time management skills
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits at research sites
Communicate with site staff including coordinators and physicians
Verify qualifications and resources of investigators and their facilities
Ensure accurate medical record verification against case report form data
Conduct on-site and remote monitoring activities with a risk-based approach
Verify eligibility of subjects for enrollment
Review regulatory documents and manage investigational product accountability
Assess patient recruitment and retention success and suggest improvements
Benefits
Competitive travel bonus
Equity and stock option program
Training completion and retention bonus
Annual merit increases
401K matching
Work-from-home opportunity
Flexible work hours
Retain airline and hotel reward points
Home office furniture allowance and equipment provided
Access to in-house travel agents and TSA pre-check reimbursement
Clear pathway to leadership positions
Comprehensive CRA training program - PACE®
Ongoing therapeutic training by in-house physicians
In-house administrative support for CRAs
Collaboration with an international team of CRAs
Full Job Description
Job Summary
Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team!
This is an exciting home-based opportunity for clinical research professionals with at least two years of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE® Training Program, you will receive the training needed to become a fully resourced CRA. You will also have the opportunity to earn a generous travel bonus, in addition to a competitive salary.
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
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 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
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
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
#LI-Remote
Please note benefits may vary based on country.
What to Expect Next
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.
About Medpace
Medpace is a clinical research organization that provides services to pharmaceutical, biotechnology, and medical device companies. The company's services include clinical trial management, regulatory consulting, and medical imaging. Medpace was founded in 1992 and is headquartered in Cincinnati, Ohio. The company has operations in North America, Europe, and Asia.
