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Clinical Research Associate (Biomedical Engineering Candidates)
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Full-time
bachelor degree
Competitive travel bonus, Equity/Stock option program, Training completion and retention bonus, Annual merit increases, 401K matching, Flexible work hours
Posted 43d ago
Apply by Jul 31
~40 hrs/week
Responsibilities
The Clinical Research Associate conducts qualification, initiation, monitoring, and closeout visits at research sites to ensure compliance with protocols and regulatory requirements. They are responsible for verifying investigator qualifications, reviewing medical records, and ensuring accurate data reporting for clinical trials.
Requirements
Candidates must hold a Bachelor’s degree in a health or science-related field, with a preference for Biomedical Engineering. The role requires the ability to travel 60-70% of the time nationwide and possess a valid driver's license.
Full job description
Join our CRA Team in Dallas, TX!
We are hiring those with Biomedical Engineering backgrounds for the CRA role!
The Clinical Research Associate position offers an exciting career within clinical research! For those with biomedical engineering 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, TX.
Medpace 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 CRA
Interactive discussions with hands-on exercises and practicums
Core departmental rotations to learn various aspects of the drug/device development and approval process
Why CRA?
Exciting travel opportunities
Make a difference on a larger scale through the development of medical drugs and devices
Dynamic working environment with varying day-to-day responsibilities
Exposure to multiple therapeutic areas
Defined CRA promotion and growth ladder
We Offer the Following:
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 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 membership, and TSA pre-check
Opportunity for leadership positions – Lead CRA, CRA 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 CRA
Opportunity to work with international team of CRAs
Responsibilities
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 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
Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance
Qualifications
Minimum of a Bachelor’s degree in a health or science related field; degree in Biomedical Engineering preffered
Ability to travel 60-70% to locations nationwide is required
A valid driver’s license and the ability to drive to monitoring sites
Minimum 1 year healthcare-related work experience preferred
Proficient knowledge of Microsoft Office
Strong communication and presentation skills
Detail-oriented and efficient in time management
Medpace Overview
Medpace 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 Work
Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
Contribute 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 approachable
Continuous Growth & Development
Office based environment with on-site mentors
Defined career paths with clear advancement opportunities
Industry renowned onboarding and training programs designed to accelerate professional development
Ongoing training and continuous learning opportunities throughout your career
An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
Competitive compensation programs that recognize and reward performance
Comprehensive health, wellness, retirement, and PTO benefits
Office based culture with occasional WFH that provides flexibility for eligible positions after training
Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A 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.
Related keywords
Clinical Research AssociateBiomedical EngineeringCROPACE Training ProgramClinical TrialsPharmaceuticalMedical DevicesGCPSOPMonitoringRegulatory AffairsData ManagementSite ManagementProtocol DeviationsAdverse EventsPatient Recruitment
Accelerating Drug, Biologic and Medical Device Clinical Development
Industry
Pharmaceutical Manufacturing
Company size
5,001-10,000 employees
Founded
1992
Headquarters
Cincinnati, OH
LinkedIn followers
376,524
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 6,500 people across 46 countries.
Offices: 5375 Medpace Way, Cincinnati, OH 45227, US
Early Phase Clinical ResearchPhase II-III Clinical ResearchRWE-Late Phase Clinical ResearchMedical Device and DiagnosticsRegulatory AffairsMedical WritingClinical MonitoringClinical Trial ManagementBiostatistics and Data SciencesDrug Safety and Pharmacovigilance
How many Healthcare jobs are open in Irving, TX right now?
There are currently 616 open healthcare positions in Irving, TX listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Healthcare roles in Irving, TX?
Companies currently hiring include McKesson Canada, Vizient, Caris Life Sciences, PDS Health, Centre for Neuro Skills, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Healthcare jobs in Irving, TX?
Yes — 173 of the 616 open healthcare positions offer remote or hybrid work (43 remote, 130 hybrid).
How do I apply for Healthcare jobs in Irving, TX?
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