Click the link below to learn more about our exciting CRA position with opportunities located Dallas, Texas!http://video.digi-me.com/digime/jobs/Healthcare/Medpace/Clinical Research Associate/MW0001MEDPACE CRA TRAINING PROGRAM (PACE)No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence:PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.PACE will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process. WE OFFER THE FOLLOWINGCompetitive travel bonusThe opportunity to work from homeRetain airline reward miles and hotel reward pointsHome office furniture allowance, laptop, mobile phone with hotspot for internet access anywhereIn-house travel agents, reimbursement for airline club, TSA pre-check, and automatic enrollment in AAAOpportunity for CRA leadership positions - Lead CRA, CRA ManagerCustomized Fast PACE training program based on your experience and therapeutic background and interestUser friendly CTMS with electronic submission and approval of monitoring visit reportsOngoing therapeutic training by our in-house physicians who are medical and regulatory expertsNationwide assignments with average of 2 protocolsIn-house administrative support for all levels of CRAsOpportunities to work with international team of CRAsMany additional perks unmatched by other CROs! Perform qualification, initiation, monitoring, and closeout visits;Establish an open line of communication with site staff;Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;Evaluate the quality and integrity of site practices - escalating quality issues as appropriate;Manage site progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution;Regulatory document review;Medical device and/or investigational product/drug accountability and inventory;Completion of follow-up activities including visit reports and follow-up letters.Minimum 1 year of nursing experience preferred;Must have at minimum a bachelor's degree in nursing;Approximately 60-80% non-local, nationwide travel is required;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; andMust be detail-oriented and efficient in time management.EO/AA Employer M/F/Disability/Vets
Website : http://www.medpace.com
A global leader in research-based drug and medical device development, Medpace builds strong strategic partnerships with select Sponsors to advance the most efficient and cost-effective path to approval. As a therapeutically-focused Contract Research Organization (CRO), we view ourselves as stewards of your drug and device, leveraging our extensive medical and regulatory expertise to deliver additional input, strategy, and efficiencies to each and every phase of the clinical trial. Medpace has the breadth, depth, and flexibility to deliver a superior result, specific to your needs, on six continents.