Clinical Research Coordinators Medpace CRA Training Program ( PACE ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Clinical Research Coordinators Medpace CRA Training Program ( PACE ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Clinical Research Coordinators Medpace CRA Training Program ( PACE ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Clinical Research Coordinators Medpace CRA Training Program ( PACE ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Clinical Research Coordinators Medpace CRA Training Program ( PACE ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Clinical Research Coordinators Medpace CRA Training Program ( PACE ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Clinical Research Coordinators Medpace CRA Training Program ( PACE ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Clinical Research Coordinators Medpace CRA Training Program ( PACE ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Clinical Research Coordinators Medpace CRA Training Program (PACE ® ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Clinical Research Coordinators Medpace CRA Training Program (PACE ® ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Clinical Research Coordinators Medpace CRA Training Program ( PACE ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
Clinical Research Coordinators Medpace CRA Training Program ( PACE ) No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.
CRA 1, IQVIA Biotech
Durham, NC · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Durham, NC · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Houston, TX · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Houston, TX · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Boston, MA · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Boston, MA · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
New York, NY · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
New York, NY · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Las Vegas, NV · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Las Vegas, NV · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Rosemont, IL · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Rosemont, IL · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
San Francisco, CA · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
San Francisco, CA · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Chicago, IL · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Chicago, IL · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Pleasant View, UT · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Pleasant View, UT · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Henderson, NV · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Henderson, NV · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Cleveland, OH · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Cleveland, OH · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Collegeville, PA · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Collegeville, PA · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Indianapolis, IN · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Indianapolis, IN · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Philadelphia, PA · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
CRA 1, IQVIA Biotech
Philadelphia, PA · On-site
$71K - $145K/yr
You will provide protocol training, set expectations, address sitelevel challenges, and support ... The CRA I prepare detailed monitoring visit reports, followup letters, and all required study ...
Cra Training information
See salary details
$11K - $22.5K
0% of jobs
$28.2K is the 25th percentile. Wages below this are outliers.
$22.5K - $34K
51% of jobs
$34K - $45.5K
13% of jobs
$45.5K - $57K
0% of jobs
$57K - $68.5K
0% of jobs
$68.5K - $80K
0% of jobs
$80K - $91.5K
0% of jobs
$91.5K - $103K
0% of jobs
$103K - $114.5K
0% of jobs
$114.5K - $126K
0% of jobs
$129.6K is the 75th percentile. Wages above this are outliers.
$126K - $137.5K
36% of jobs
$11K
$79.4K
$137.5K
How much do cra training jobs pay per year?
What is the difference between Cra Training vs Clinical Research Associate?
| Aspect | Cra Training | Clinical Research Associate |
|---|---|---|
| Required Credentials | Training programs, certifications (e.g., CCRP) | Typically requires a degree in life sciences and certification |
| Work Environment | Classroom, online courses, training sessions | Monitoring sites, data review, site communication |
| Industry Usage | Prepares individuals for clinical research roles | Performs monitoring and oversight in clinical trials |
Cra Training provides foundational education and certifications to prepare individuals for roles in clinical research. A Clinical Research Associate (CRA) is a professional who applies this training by monitoring clinical trials, ensuring compliance, and managing site activities. While Cra Training is focused on education, a CRA is an active role within the industry, often requiring prior training or certification.
What is CRA training?
What are some common challenges faced during CRA training and how can trainees overcome them?
How to become a certified CRA?
What qualifications do I need to be a CRA?
What are the key skills and qualifications needed to thrive as a Clinical Research Associate (CRA), and why are they important?

Other
Medical, Retirement, PTO
Re-posted 19 days ago
Medpace rating
8.6
Based on 12 frontline employees who took The Breakroom Quiz
14th of 72 rated research
Job description
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:
- Nursing
- Dietetics
- Nutrition Science
- Pharmaceutical/Device Sales Representative
- Physical and Occupational Therapists
- Biomedical/Chemical Engineer
- Public Health
- PhD/Post-Doc
- Pharm.D
- Health and Wellness Education Coordinators
- Research Assistants
- Clinical Research Coordinators
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
- 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
- Minimum of a Bachelor's degree in a health or science related field
- 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 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 its 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 6,000 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.
Dallas Perks
- Dallas Campus Overview
Flexible work environment
Competitive PTO packages, starting at 20+ days
Competitive compensation and benefits package
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Community involvement with nonprofit organizations
Structured career paths with opportunities for professional growth
Discounts on local sports games, fitness gyms and attractions
Modern, ecofriendly campus with an on-site fitness center
Free on-site parking
Outdoor seating and workspace
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.
Employment Type: OTHERAbout Medpace
Sourced by ZipRecruiter
Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.
Industry
Medical equipment and supplies manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1992