Medpace
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Medpace, Miami, Florida, us, 33222
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Job Locations:United States-AZ-Phoenix | United States-OH-Cincinnati | United States-TX-Irving (Dallas) | United States-UT-Salt Lake City | United States-TX-Houston | United States-TX-Austin | United States-TN-Nashville | United States-Miami | United States-PA-Philadelphia | United States-MOJob Summary
Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team! This is an exciting opportunity for clinical research professionals with at least one year 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 functional CRA with the opportunity to work home-based. 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;The 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, and TSA pre-check;Opportunity for leadership positions - Lead CRA, CRA Manager, Clinical Trial 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 CRAs;Opportunities to work with an international team of CRAs.Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;Communicate 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;Perform medical record and research source documentation verification against case report form data, ensuring good documentation practices are adhered to;Conduct on-site and virtual/remote monitoring activities to identify site deviations/deficiencies and corrective/preventive actions;Verify that the investigator is enrolling only eligible subjects;Review regulatory documents;Accountability and inventory for medical devices and/or investigational products/drugs;Verify and review adverse events, serious adverse events, and concomitant medications for accurate data reporting;Assess the clinical research site's patient recruitment and retention success and offer suggestions for improvement;Complete monitoring reports and follow-up letters summarizing significant findings, deviations, deficiencies, and recommended actions.Qualifications
Must have a minimum of a Bachelor's degree in a health or science-related field;Experience as a Clinical Research Coordinator (minimum 1 year);Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely;Must maintain a valid driver's license and the ability to drive to monitoring sites;Proficient knowledge of Microsoft Office;Strong communication and presentation skills;Must be detail-oriented and efficient in time management.#LI-RemoteMedpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks:Hybrid work-from-home options (dependent upon position and level);Competitive PTO packages - starting at 20+ days;Company-sponsored employee appreciation events;Employee health and wellness initiatives;Flexible work schedule;Competitive compensation and benefits package;Structured career paths with opportunities for professional growth;Discounts for local businesses.Awards:Named a Top Workplace in 2024 by The Cincinnati Enquirer;Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024;Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.What to Expect Next:A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets
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Job Locations:United States-AZ-Phoenix | United States-OH-Cincinnati | United States-TX-Irving (Dallas) | United States-UT-Salt Lake City | United States-TX-Houston | United States-TX-Austin | United States-TN-Nashville | United States-Miami | United States-PA-Philadelphia | United States-MOJob Summary
Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team! This is an exciting opportunity for clinical research professionals with at least one year 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 functional CRA with the opportunity to work home-based. 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;The 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, and TSA pre-check;Opportunity for leadership positions - Lead CRA, CRA Manager, Clinical Trial 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 CRAs;Opportunities to work with an international team of CRAs.Responsibilities
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;Communicate 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;Perform medical record and research source documentation verification against case report form data, ensuring good documentation practices are adhered to;Conduct on-site and virtual/remote monitoring activities to identify site deviations/deficiencies and corrective/preventive actions;Verify that the investigator is enrolling only eligible subjects;Review regulatory documents;Accountability and inventory for medical devices and/or investigational products/drugs;Verify and review adverse events, serious adverse events, and concomitant medications for accurate data reporting;Assess the clinical research site's patient recruitment and retention success and offer suggestions for improvement;Complete monitoring reports and follow-up letters summarizing significant findings, deviations, deficiencies, and recommended actions.Qualifications
Must have a minimum of a Bachelor's degree in a health or science-related field;Experience as a Clinical Research Coordinator (minimum 1 year);Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely;Must maintain a valid driver's license and the ability to drive to monitoring sites;Proficient knowledge of Microsoft Office;Strong communication and presentation skills;Must be detail-oriented and efficient in time management.#LI-RemoteMedpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace Perks:Hybrid work-from-home options (dependent upon position and level);Competitive PTO packages - starting at 20+ days;Company-sponsored employee appreciation events;Employee health and wellness initiatives;Flexible work schedule;Competitive compensation and benefits package;Structured career paths with opportunities for professional growth;Discounts for local businesses.Awards:Named a Top Workplace in 2024 by The Cincinnati Enquirer;Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024;Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.What to Expect Next:A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.EO/AA Employer M/F/Disability/Vets
#J-18808-Ljbffr