Clinical Research Associate – Cincinnati, OH (Entry-Level)
About the position
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol.
Communicate with medical site staff including coordinators and clinical research physicians.
Verify adequate investigator qualifications, training, and resources, including facilities and staff.
Perform medical record and research source documentation verification against case report form data.
Conduct on-site and virtual monitoring activities with a risk-based approach.
Ensure the investigator is enrolling only eligible subjects.
Review regulatory documents and ensure compliance with protocols.
Manage medical device and investigational product accountability and inventory.
Verify and review adverse events and ensure accurate data reporting.
Assess patient recruitment and retention success and suggest improvements.
Complete monitoring reports and follow-up letters summarizing findings and recommended actions.
Requirements
Bachelor's degree in a health or science-related field; advanced degrees or prior clinical research experience is a plus.
Ability to travel 60-70% to locations nationwide.
Valid driver's license and ability to drive to monitoring sites.
Proficient knowledge of Microsoft® Office.
Strong communication and presentation skills.
Detail-oriented and efficient in time management.
Nice-to-haves
Advanced degrees in health or science-related fields.
Prior clinical research experience.
Benefits
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
Home office furniture allowance
In-house travel agents and reimbursement for airline club
Opportunities for leadership positions
Ongoing therapeutic training by in-house physicians
In-house administrative support for CRAs
Opportunities to work with an international team of CRAs.
Apply Now
Apply Now
Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol.
Communicate with medical site staff including coordinators and clinical research physicians.
Verify adequate investigator qualifications, training, and resources, including facilities and staff.
Perform medical record and research source documentation verification against case report form data.
Conduct on-site and virtual monitoring activities with a risk-based approach.
Ensure the investigator is enrolling only eligible subjects.
Review regulatory documents and ensure compliance with protocols.
Manage medical device and investigational product accountability and inventory.
Verify and review adverse events and ensure accurate data reporting.
Assess patient recruitment and retention success and suggest improvements.
Complete monitoring reports and follow-up letters summarizing findings and recommended actions.
Requirements
Bachelor's degree in a health or science-related field; advanced degrees or prior clinical research experience is a plus.
Ability to travel 60-70% to locations nationwide.
Valid driver's license and ability to drive to monitoring sites.
Proficient knowledge of Microsoft® Office.
Strong communication and presentation skills.
Detail-oriented and efficient in time management.
Nice-to-haves
Advanced degrees in health or science-related fields.
Prior clinical research experience.
Benefits
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
Home office furniture allowance
In-house travel agents and reimbursement for airline club
Opportunities for leadership positions
Ongoing therapeutic training by in-house physicians
In-house administrative support for CRAs
Opportunities to work with an international team of CRAs.
Apply Now
Apply Now