Clinical Research Associate (CRA) - Dallas
Medpace
Join Our CRA Team in Dallas, Texas!The Clinical Research Associate position offers an exciting career within clinical research! For those with medical and life science backgrounds wanting to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this is the right opportunity for you!This position is office based in Dallas, Texas.Our successful Clinical Research Associates possess various backgrounds within the medical, healthcare, and science-related fields:NursingDieteticsNutrition SciencePharmaceutical/Device Sales RepresentativePhysical and Occupational TherapistsBiomedical/Chemical EngineerPublic HealthPhD/Post-DocPharm.DHealth and Wellness Education CoordinatorsResearch AssistantsClinical Research CoordinatorsMedpace CRA Training Program (PACE®)No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. The PACE® (Professionals Achieving CRA Excellence) Training Program includes the following:A platform to effectively and confidently carry out CRA duties to ultimately become a high-functioning, independent, Medpace CRAInteractive discussions with hands-on exercises and practicumsCore departmental rotations to learn various aspects of the drug/device development and approval processWhy CRA?Exciting travel opportunitiesMake a difference on a larger scale through the development of medical drugs and devicesDynamic working environment with varying day-to-day responsibilitiesExposure to multiple therapeutic areasDefined CRA promotion and growth ladderWe Offer the Following:Competitive travel bonusEquity/Stock option programTraining completion and retention bonusAnnual merit increases401K matchingOpportunity to work from homeFlexible work hours across days within a weekRetain 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 membership, and TSA pre-checkOpportunity for leadership positions – Lead CRA, CRA Manager, Training and Development Manager, and many moreCRA training program - PACE®Ongoing therapeutic training by our in-house physicians who are medical and regulatory expertsIn-house administrative support for all levels of CRAOpportunity to work with international team of CRAsResponsibilitiesConduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocolCommunication with the medical site staff including coordinators, clinical research physicians, and their site staffVerify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staffMedical 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 requirementsOn-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 forwardVerification the investigator is enrolling only eligible subjectsRegulatory document reviewMedical device and/or investigational product/drug accountability and inventoryVerification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocolAssess the clinical research site's patient recruitment and retention success and offering suggestions for improvementCompletion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure complianceQualificationsMinimum of a Bachelor's degree in a health or science related fieldAbility to travel 60-70% to locations nationwide is requiredA valid driver's license and the ability to drive to monitoring sitesMinimum 1 year healthcare-related work experience preferredProficient knowledge of Microsoft OfficeStrong communication and presentation skillsDetail-oriented and efficient in time managementMedpace OverviewMedpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.Why Medpace?When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.Purpose-Driven WorkWork alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellenceCollaborative CultureContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.Leadership throughout Medpace is both accessible and approachableContinuous Growth & DevelopmentOffice based environment with on-site mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quicklyOther Employee BenefitsCompetitive compensation programs that recognize and reward performanceComprehensive health, wellness, retirement, and PTO benefitsOffice based culture with occasional WFH that provides flexibility for eligible positions after trainingCompany-sponsored social eventsPlease note benefits may vary based on country.What to Expect NextA 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.
- ...Join Our CRA Team in Dallas, Texas! The Clinical Research Associate position offers an exciting career within clinical research! For those with medical and life science backgrounds wanting to explore the research field, travel the US, and be part of a team bringing...SuggestedContract workWork experience placementWork at officeRemote workWork from homeHome officeFlexible hours
$40k
...Clinical Research Associate IThis is a grant funded position with an end date of 12/31/2026, renewable based upon availability of funding, work performance... ...for clinical research.The Clinical Research Associate I (CRA I) is responsible for assisting in the planning, execution,...SuggestedInternshipWork at officeWeekend workAfternoon shift$71.9k - $169.3k
IQVIA Biotech is now hiring for CRA 2 with a minimum of 1 year of on-site monitoring and will also consider CRA 1 candidates... ...to patients faster.Job OverviewWe are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key role in ensuring the...SuggestedFull timePart timeImmediate startWorldwide$40k
...Job Posting Title: Clinical Research Associate I ---- Hiring Department: Department of Psychiatry ---- Position Open To: All Applicants... ...goals. Purpose The Clinical Research Associate I (CRA I) provides foundational operational support for clinical...SuggestedFull timeFor contractorsInternshipWork at officeRemote work- Job Purpose The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study...SuggestedLocal areaRemote workFlexible hoursShift work
- The Clinical Research Associate (CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical...Local areaRemote work
$40k
Clinical Research Associate I Department: Psychiatry, University of Texas at Austin Location: Austin, TX Weekly Hours: 40 Full Time: Exempt Start... ...requirements and study protocols. The Clinical Research Associate I (CRA I) will work independently or with general direction at the...Full timeFor contractorsWork at officeImmediate startAfternoon shift- The University of Texas at Austin invites applications for a Clinical Research Associate I in the Psychiatry department. This full-time exempt on-... ...to ensure protocol adherence and regulatory compliance. The CRA I will manage sites, collect data in REDCap, help prepare...Full time
$89k - $148k
...interact with their digital world.Team Description:The Neuralink Clinical team is at the heart of an ecosystem that merges... ...in people!Job Description and Responsibilities:As a Clinical Research Associate, you'll play a crucial role in pioneering groundbreaking clinical...Full timeTemporary workInterim roleRemote work- Parexel in Austin, Texas is seeking a Clinical Research Associate (CRA) responsible for overseeing clinical studies at assigned sites. You will ensure compliance with ICH-GCP and work closely with local study teams. The successful candidate will manage site selection,...Local area
- ...Specialist, Diasorin continuously invests in research, technology, and people. Guided by our... ...Job Scope The Clinicial Research Associate will be responsible for conducting day-to... ...day work associated with analytical and clinical studies conducted by Luminex, A DiaSorin...Full timeWork experience placementSecond jobLocal areaWorldwide
- ...Medical Park Tower Department/Specialty: Research Cardiology Schedule: Full time | Monday... ...'ll make an impact in this role Drive Clinical Trial Lifecycle: Co-design, administer,... ...with 2 years of cumulative experience OR Associate's degree/Technical degree OR 4 years of...Full timeTemporary workLocal areaMonday to Friday
- A premier academic institution in Austin is seeking a Clinical Research Coordinator to oversee various aspects of clinical trials. The ideal candidate will ensure compliance with protocols, manage site performance, and coordinate participant schedules. A Bachelor's degree...
- ...senior staff oversight.* Coordinates with clinical staff for specimen collection and... ...Assists in the training of new site staff and research team members.* Participates in internal... ...guidelines.* Certified Clinical Research Associate (CCRA) or Certified Clinical Research...InternshipWork at officeLocal area
$40k
A prominent educational institution in Austin, Texas, seeks a Clinical Research Associate I to oversee clinical research projects and manage participant recruitment. This role involves ensuring regulatory compliance and coordinating with clinical staff for research activities...- A leading educational institution in Texas is seeking a Clinical Research Associate I responsible for managing and overseeing clinical research projects. This position entails significant involvement in recruitment and data collection while ensuring compliance with regulatory...
- Ascension in Austin, TX is seeking a Research Cardiology professional to drive the clinical trial lifecycle, co-design protocols, administer studies, and monitor daily activities to ensure seamless execution. You will manage regulatory documentation, maintain informed...
- Urology Alliance is seeking a dedicated Clinical Research Coordinator to support protocol-specific procedures and documentation. You will work with study coordinators and the research team to conduct screenings, manage visits, and ensure adherence to study requirements,...
- The University of Texas at Austin, Dell Medical School, seeks a Clinical Research Associate I to support clinical trials under supervision. The role focuses on site monitoring, data quality checks, and regulatory document management, with potential for renewal based on...
- University of Texas at Austin is seeking a Clinical Research Associate I to support clinical trials within the Psychiatry department. The role focuses on site coordination, participant recruitment, data integrity, and regulatory compliance. This grant-funded position requires...
- ...Clinical Research Assistant IOur goal is to advance retinal research, offer new treatment opportunities to our community, and provide the highest quality patient care. Austin Retina Associates is seeking curious and patient-focused individuals for a Clinical Research...Work at office
$40k
...Research Associate I Dell Medical School is seeking a Research Associate I. This position is temporary with an end date of... ...techniques used in the research area. Certification as a Clinical Research Associate (CRA) from the Association of Clinical Research...Temporary workCasual workWork at officeAfternoon shift$18 - $24 per hour
...Clinical Research Assistant (Round Rock) Are you a skilled ophthalmic technician and passionate about the advancement of Ophthalmology?... ...individuals like you! Join our dedicated team at Austin Retina Associates, at the forefront of ophthalmic innovation. We are committed...Hourly payFull time$20 per hour
...Dallas/Ft. Worth Part-time Operations Assistant, Texas McCombs Under direct to general supervision, this part-time Dallas- Fort Worth based role will provide university employees, students, and faculty with technical assistance, support, advice, as well as policy and...Hourly payPart timeCasual workWork at officeShift workWeekend workAfternoon shift$21.63 - $26.44 per hour
...Public Health Sciences (PHS) is the home for the core quantitative research fields in public health: biostatistics, epidemiology and health... ...public health scholars and professionals. Job Summary The Clinical Sr. Research Assistant will oversee key aspects of clinical research...Hourly payWork experience placement- Bilingual Clinical Research Assistant (Path to Clinical Research Coordinator) Austin, TX Bilingual (English/Spanish) Clinical Research Assistant to join our Austin team. This role is ideal for someone looking to build a long-term career in clinical research, with hands...Local areaFlexible hours
- A clinical research organization in Austin is seeking a Bilingual Clinical Research Assistant to support clinical trials and collect patient data. This role is perfect for those looking to advance into a Clinical Research Coordinator position. Responsibilities include assisting...
- Clinical Research Assistant Job at Diasorin, USA | Biology Candidates, Apply Now Clinical Research Assistant Job at Diasorin, USA. Biology... ...External Study Execution: Managing day‑to‑day hands‑on work associated with analytical method validation and clinical trials for in...Full timeWork experience placementWorldwideRelocationShift work
- The University of Chicago seeks a Clinical Sr. Research Assistant to oversee key aspects of clinical research, including subject recruitment, data collection, and database development. This role supports data analysis, manuscript preparation, and adherence to study protocols...Hourly pay
- Under general direction of the Laboratory Supervisor or Director, the Embryologist II or III, performs advanced technical clinical and research duties independently in the embryology laboratory. Interacts directly with physicians and demonstrates ability to use own judgement...Extra incomeFull timeWork experience placementRelocation packageWeekend work
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