Clinical Research Associate (CRA) - Dallas
Behavioral Health Market Context
Benefits
This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devicesDynamic working environment, with varying responsibilities day-to-dayDefined CRA promotion and growth ladder with potential for mentoring and management advancementsCompetitive pay and many additional perks unmatched by other CROs (SEE BELOW)WE OFFER THE FOLLOWINGCompetitive travel bonus;Equity/Stock Option Program;Training completion and retention bonusAnnual 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; andOpportunities to work with international team of CRAsFlexible work environmentCompetitive PTO packages, starting at 20+ daysCompetitive compensation and benefits packageCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesCommunity involvement with nonprofit organizationsStructured career paths with opportunities for professional growthDiscounts on local sports games, fitness gyms and attractionsModern, ecofriendly campus with an on-site fitness centerFree on-site parkingOutdoor seating and workspace28 more items(s)
Qualifications
- •No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs
- •Expansive experience in multiple therapeutic areas
- •Work within a team of therapeutic and regulatory experts
- •Ability to travel 60-70% to locations nationwide is required, or less if remote/virtual visits 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; and
- •Must be detail-oriented and efficient in time management
- •Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
- •6 more items(s)
Responsibilities
- •Pharmaceutical/Device Sales Representative
- •Health and Wellness Education Coordinators
- •Research Assistants
- •MEDPACE CRA TRAINING PROGRAM (PACE)
- •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
- •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 that 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; and
- •Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance
- •15 more items(s)
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