Average Clinical Research Associate (CRA) Salary at Medpace, Inc.

The average salary for a Clinical Research Associate (CRA) is $56,415 in 2024

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What is the pay by experience level for clinical research associate (cra)s .

An entry-level Clinical Research Associate (CRA) with less than 1 year experience can expect to earn an average total compensation (includes tips, bonus, and overtime pay) of $50,209 based on 23 salaries. An early career Clinical Research Associate (CRA) with 1-4 years of experience earns an average total compensation of …Read more

What Do Clinical Research Associate (CRA)s Do?

Clinical research associates (CRA) are responsible for assisting in the clinical research process, providing advanced technical expertise in steps such as handling supplies, ordering tests, and collecting results, presenting specific research information to the public, and a variety of administrative tasks. CRAs must follow strict privacy and safety regulations to prevent problems with subjects and ethical concerns; they must also be organized and pay close attention to detail when conducting …Read more

Common Health Benefits for a Clinical Research Associate (CRA)

Gender breakdown for clinical research associate (cra)s.

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FAQs About Clinical Research Associate (CRA)s

What is the highest pay for clinical research associate (cra)s.

Our data indicates that the highest pay for a Clinical Research Associate (CRA) is $88k / year

What is the lowest pay for Clinical Research Associate (CRA)s?

Our data indicates that the lowest pay for a Clinical Research Associate (CRA) is $44k / year

How can Clinical Research Associate (CRA)s increase their salary?

Increasing your pay as a Clinical Research Associate (CRA) is possible in different ways. Change of employer: Consider a career move to a new employer that is willing to pay higher for your skills. Level of Education: Gaining advanced degrees may allow this role to increase their income potential and qualify for promotions. Managing Experience: If you are a Clinical Research Associate (CRA) that oversees more junior Clinical Research Associate (CRA)s, this experience can increase the likelihood to earn more.

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What Does a Medpace Clinical Research Associate Do?

Find out what a Medpace Clinical Research Associate does, how to get this job, and what it takes to succeed as a Medpace Clinical Research Associate.

clinical research associate medpace salary

Medpace is a global clinical research organization that provides comprehensive clinical development services to the biopharmaceutical and medical device industries. They specialize in providing clinical trial management, regulatory affairs, data management, and other services to help bring new treatments to market.

A Clinical Research Associate at Medpace is responsible for managing clinical trials from start to finish. This includes developing study protocols, recruiting and training study staff, monitoring study sites, and ensuring compliance with all applicable regulations. The Clinical Research Associate is also responsible for collecting and analyzing data, preparing reports, and presenting results to the client.

Medpace Clinical Research Associate Job Duties

A Medpace Clinical Research Associate typically has a wide range of responsibilities, which can include:

  • Monitor clinical trials in accordance with Good Clinical Practice (GCP) and applicable regulations
  • Ensure that all study-related activities are conducted according to the protocol, SOPs, ICH/GCP guidelines, and local regulations
  • Perform site selection, initiation, monitoring, and closeout visits for assigned studies
  • Prepare and submit visit reports within specified timelines
  • Review source documents for accuracy and completeness
  • Track regulatory documents and ensure timely submission of required documents
  • Assist in the development of project plans and budgets
  • Provide guidance and training to sites on protocol requirements and GCP compliance
  • Maintain effective communication with internal teams and external vendors
  • Monitor data entry into electronic databases and review data listings for accuracy
  • Participate in investigator meetings as needed
  • Develop and maintain relationships with investigative sites

Medpace Clinical Research Associate Salary

The salary of a Clinical Research Associate at Medpace is determined by a variety of factors, including the individual’s experience and qualifications, the complexity of the job, the geographic location of the position, and the company’s budget. Additionally, the company may take into consideration the cost of living in the area, the availability of similar positions in the area, and the overall market demand for the position.

  • Median Annual Salary: $82,926 ($39.87/hour)
  • Top 10% Annual Salary: $112,270 ($53.98/hour)

Medpace Clinical Research Associate Job Requirements

To be hired as a Clinical Research Associate at Medpace, applicants must have a Bachelor’s degree in a scientific field, such as biology, chemistry, or a related field. Previous experience in clinical research is preferred, but not required. Additionally, applicants must have excellent communication and organizational skills, as well as the ability to work independently and as part of a team. Certification in Good Clinical Practice (GCP) is also preferred, but not required. Finally, applicants must be able to travel up to 25% of the time, as some clinical research sites may be located outside of the local area.

Medpace Clinical Research Associate Skills

Medpace Clinical Research Associate employees need the following skills in order to be successful:

Site Initiation Visits (SIVs): SIVs are the first time a clinical research associate visits a research site to assess its suitability for clinical trials. This is an important part of the job, as it ensures the site meets the standards of the clinical research industry. Clinical research associates must be able to assess a site’s facilities, staff and resources to determine if it’s a good fit for clinical trials.

Informed Consent: Informed consent is the process by which a research participant is informed about the details of a study, including the potential risks and benefits of participating. Clinical research associates must be able to explain study details to participants in a way that is clear and easy to understand. This requires clinical research associates to have a thorough understanding of the study protocol and procedures.

IRB: An associate working in a clinical research company’s IRB (Institutional Review Board) is responsible for ensuring that the company follows all regulations and laws regarding the treatment of human subjects. This position requires a thorough understanding of the regulations and laws, as well as the ability to interpret and apply them to the company’s research.

Good Clinical Practice (GCP): GCP is a set of standards that clinical research associates must follow to ensure the integrity of a study. These standards include ethical treatment of patients, accurate data collection and reporting and compliance with all regulations. Clinical research associates must be familiar with GCP to ensure the quality of the data they collect and the safety of the patients involved in the study.

Ethics Committee Approval Process: Clinical research associates must follow ethical guidelines when conducting research. This includes ensuring the safety of the participants and ensuring the research follows the guidelines set by the committee. Clinical research associates must also follow ethical guidelines when recording data and maintaining confidentiality.

Medpace Clinical Research Associate Work Environment

Medpace Clinical Research Associates (CRA) typically work in an office setting, but may also travel to clinical sites to monitor clinical trials. CRA’s typically work 40 hours per week, but may be required to work additional hours to meet deadlines or to complete tasks. CRA’s may also be required to travel to clinical sites to monitor clinical trials, which may require overnight stays. CRA’s must be able to work in a fast-paced environment and handle multiple tasks simultaneously. They must also be able to work independently and be able to handle stressful situations.

Medpace Clinical Research Associate Trends

Here are three trends influencing how Medpace Clinical Research Associate employees work.

Data Management

Data management is becoming increasingly important in the clinical research field. Medpace Clinical Research Associates must be able to manage and analyze large amounts of data from multiple sources, including patient records, laboratory results, and medical images. They must also be able to interpret this data accurately and efficiently.

Data management tools are being developed to help streamline the process of collecting, organizing, and analyzing data. These tools can help reduce errors and improve accuracy, as well as provide insights into trends that may not have been previously visible. As such, it is essential for Medpace Clinical Research Associates to understand how to use these tools effectively in order to maximize their efficiency and effectiveness.

The Role of the CRA During and After COVID-19

The role of the Clinical Research Associate (CRA) has become increasingly important during and after the COVID-19 pandemic. As clinical trials have been disrupted due to the pandemic, CRAs are now tasked with ensuring that protocols are followed and data is collected accurately.

CRAs must also be able to adapt quickly to changing regulations and guidelines in order to ensure compliance. Additionally, they must be able to effectively communicate with sponsors and sites to ensure that all parties involved understand the protocol and can work together to achieve successful outcomes.

The CRA’s role will continue to evolve as the industry recovers from the pandemic. It is essential for CRAs to stay up to date on new technologies and trends in order to remain competitive and provide the best possible service to their clients.

Patient Engagement in Clinical Trials

Patient engagement in clinical trials is becoming increasingly important as the healthcare industry shifts to a more patient-centric approach. Medpace Clinical Research Associates are at the forefront of this trend, working with patients and their families to ensure that they understand the risks and benefits associated with participating in a trial.

Patient engagement also helps to improve data quality by providing real-time feedback on how the trial is progressing. This allows for better decision making and faster results. Additionally, it can help to reduce costs associated with running a trial by reducing the need for additional resources or personnel. By understanding the importance of patient engagement, Medpace Clinical Research Associates will be well positioned to take advantage of this emerging trend.

Advancement Prospects

Clinical research associates can advance their careers by taking on more responsibility and gaining experience in different areas of clinical research. They may move up to a supervisory role, such as a clinical research manager, or they may move into a more specialized role, such as a clinical research coordinator or a clinical research scientist. They may also choose to pursue a higher degree in clinical research or a related field, such as a Master’s degree in Clinical Research Administration.

Interview Questions

Here are five common Medpace Clinical Research Associate interview questions and answers.

1. How would you handle an irate client?

This question can help interviewers assess your interpersonal skills and ability to handle challenging situations. In your answer, try to show that you have the patience and problem-solving skills to diffuse a tense situation and resolve it quickly.

Example: “I would first listen carefully to what they’re saying and ask questions if I don’t understand something. Then, I’d explain in simple terms why their concerns aren’t valid or how we are working on resolving them. If they continue to be upset, I would offer to speak with them privately so no one else has to hear their complaints.”

2. Have you worked with any regulatory documents before? What kind?

This question can help the interviewer understand your experience with regulatory documents and how you apply them to your work. You can use examples from previous jobs to show that you know what a regulatory document is, how it works and how to apply it to your research.

Example: “I have worked with several regulatory documents in my past roles as a clinical research associate. I’ve worked with both FDA and IRB regulations for all of my projects, which has helped me ensure that our company’s research was safe and ethical. I also used GCP guidelines when working on studies abroad, where we had to comply with local laws.”

3. What are some of your skills that would help make you successful as a Clinical Research Associate?

This question is an opportunity to highlight your relevant skills and abilities. When answering this question, it can be helpful to include a brief description of the skill or ability along with an example from your experience that shows how you use it.

Example: “I have excellent organizational skills, which I developed through my previous role as a medical records clerk at a hospital. This helped me keep track of patient information and ensure all documents were filed correctly. Another skill I possess is my attention to detail, which has helped me notice errors in data entry before sending reports to clients.”

4. What is your experience with data collection and management?

This question can help the interviewer understand your experience with clinical research and how you might fit into their team. Use examples from your previous job to highlight your skills, but also consider including any personal projects or volunteer work that helped you develop these skills.

Example: “In my last position as a medical researcher, I was responsible for collecting data on patient demographics, health history and treatment plans. This involved entering information into our database and ensuring it was accurate before sending it to the lead researchers. I also worked closely with other members of the team to ensure we were all using the same terminology when recording data.”

5. Tell me about a time when you were under a lot of pressure at work, what did you do to manage it?

This question can help the interviewer get a better idea of how you handle stressful situations. Use your answer to highlight your ability to work under pressure and remain calm, focused and productive.

Example: “I once had an extremely busy week at my previous job where I was working on several projects at once. One day, I received a call from one of our clients who needed some additional information about their study. I told them that I would look into it right away and find out what they needed. After finishing up with all of my other tasks for the day, I looked over the client’s file again and found the information they were looking for. They were very happy with my response.”

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MEDPACE Clinical Research Associate-Dallas Entry Level Salary in the United States

How much does an Clinical Research Associate-Dallas Entry Level make at companies like MEDPACE in the United States? The average salary for Clinical Research Associate-Dallas Entry Level at companies like MEDPACE in the United States is $86,567 as of January 26, 2024, but the range typically falls between $74,919 and $98,214 . Salary ranges can vary widely depending on many important factors, including education, certifications, additional skills, the number of years you have spent in your profession. With more online, real-time compensation data than any other website, Salary.com helps you determine your exact pay target.  View the Cost of Living in Major Cities2

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What does an Clinical Research Associate-Dallas Entry Level do at companies like MEDPACE?

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. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 3,000 people across 36 countries.

Job Summary

The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a  medical and/or health/life science background who want to explore the research field, travel the US , and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

Our successful Clinical Research Associates possess various backgrounds in medical and other science-related healthcare fields. Backgrounds of individuals who have succeeded in the CRA role include:

  • Pharmacy Technician/Pharmacist
  • Pharmaceutical/Device Sales Representative
  • Biomedical/Chemical Engineer
  • PhD/Post-Doc
  • Pharm.D candidates
  • Health and Wellness Coordinators
  • Research Assistants

MEDPACE 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  P rofessionals A chieving C RA E xcellence:

  • 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. 

WHY BECOME A CRA

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 devices.  The CRA position provides many other distinctive advantages including:

  • Dynamic working environment, with varying responsibilities day-to-day
  • Expansive experience in multiple therapeutic areas
  • Work within a team of therapeutic and regulatory experts
  • Defined CRA promotion and growth ladder with potential for mentoring and management advancements
  • Competitive pay and opportunity for significant travel bonus

WE OFFER THE FOLLOWING

  • Competitive travel bonus
  • The opportunity to work from home
  • 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, TSA pre-check, and automatic enrollment in AAA
  • Opportunity for CRA leadership positions – Lead CRA, CRA Manager
  • Customized Fast PACE training program based on your experience and therapeutic background and interest
  • User friendly CTMS with electronic submission and approval of monitoring visit reports
  • Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
  • Nationwide assignments with average of 2 protocols
  • In-house administrative support for all levels of CRAs
  • Opportunities to work with international team of CRAs
  • Many additional perks unmatched by other CROs!

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;
  • 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.

Qualifications

  • Must have a minimum of a bachelor’s degree in a health or science related field;
  • Approximately 60-80% non-local, nationwide travel is required;
  • Must maintain a valid driver’s license and the ability to drive to monitoring sites;
  • Minimum 1 year relevant work experience preferred;
  • Proficient knowledge of Microsoft® Office;
  • Strong communication and presentation skills; and
  • Must be detail-oriented and efficient in time management.

Why Medpace?

When you join Medpace, you become part of a team dedicated to supporting the development of ground breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities. 

  • Medpace Named a Top Cincinnati Workplace for 2015, 2016, 2017 and 2018 by the Cincinnati Enquirer
  • Winner of the ACRP-Avoca CRO Quality Award in 2018
  • Recognized with six CRO Leadership Awards from Life Science Leader magazine
  • Eagle Award winner - which recognizes outstanding leadership, professionalism, integrity, and dedication to advancing the clinical research profession through strong site partnerships

What to Expect Next

We look forward to receiving your application.  A member of our recruitment team will review your qualifications and if interested, you will be contacted for an interview.

EO/AA Employer M/F/Disability/Vets

*WARNING: Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money.  These scammers pose as legitimate employees from actual companies.  Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process.

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Nursing in Clinical Research: Cody McClanahan Pulls Back the Curtain

  • May 12, 2023

clinical research associate medpace salary

“To put it simply, I wanted to help people,” says Clinical Research Associate (CRA) Manager Cody McClanahan, RN, BSN. Today, Cody is a CRA Manager at Medpace, but he actually began his career as a nurse caring for patients at a hospital. It wasn’t until he learned that clinical research could broaden his reach to patients all around the world that he began to explore such paths.  

As a bedside nurse, Cody wasn’t aware a path existed for nurses in clinical research. He was first introduced to Contract Research Organizations (CROs) by a coworker, but what really piqued his interest was the scope of patients he could reach through clinical research. “…I was making a positive impact on the lives of four to five patients I interacted with each day.” Cody shares that, at the time, he was working with patients recovering from various urologic procedures on the Urology floor. “However, the thought of joining Medpace and playing a part in the development of safe and effective therapeutics that could improve the lives of millions was compelling.”

When considering having a hand in impacting the lives of people around the world, Cody found himself unable to pass up the opportunity. Ready to make a change, he applied to Medpace and accepted a role as a CRA. As he waited to begin his first day as a CRA, Cody initially anticipated that his time would be filled with administrative tasks and that his arsenal of nursing knowledge might be underutilized. However, he discovered this to be far from the truth: he routinely worked with physicians, pharmacists, fellow nurses, and many other healthcare professionals. Cross-departmental collaboration is essential to develop comprehensive care plans for participating patients to ensure their safety. Following his first week on the job, he “realized it was the perfect fit for me and never looked back.”

“Playing a part in the development of safe and effective therapeutics that could improve the lives of millions was compelling.”

In his previous role as a CRA, Cody monitored clinical research sites and worked to certify that the collected data was accurate. Now as a CRA Manager, Cody manages a broader range of responsibilities. Among team management, cross-functional collaboration, and assuring patient safety throughout the trial process, he also works much closer with his CRA team. Cody provides guidance and training to his team, and he ensures studies are conducted within local regulations and company policies.

Cody was two years into his nursing career before he learned about the vast opportunities open to nurses, and he wants to change this for the next generation of nurses. Both new and seasoned nurses should “note that even if the first position you come across doesn’t seem like the right fit, there are still many more options to explore…It’s about finding the right fit for you.” Career paths aren’t a ‘one size fits all,’ and Cody encourages those considering careers as nurses in clinical research to “dive in headfirst.”

While he no longer plays a hands-on role in patient care as he did at the hospital, Cody is still able to interact with patients and “witness firsthand the positive impact our investigational products are having on their daily lives and activities.” Cody joined the field of clinical research with the same goal that drove him to become a nurse: to help people. And each day at Medpace he does just that.

clinical research associate medpace salary

Medpace careers

Clinical Research Associate

clinical research associate medpace salary

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COMMENTS

  1. Medpace Clinical Research Associate Salaries

    $72K - $108K / yr Base Pay

  2. How Much Does Medpace Pay in 2024? (2,230 Salaries)

    Interviews 313 Benefits 42 Photos 492 Diversity + Add a Salary Medpace Salaries How much do Medpace employees make? Glassdoor has salaries, wages, tips, bonuses, and hourly pay based upon employee reports and estimates. Research & Science 1K Salaries submitted Clinical Research Associate 273 salaries Statistical Analyst 68 salaries View More >

  3. Medpace Clinical Research Associate I Salaries

    The estimated total pay range for a Clinical Research Associate I at Medpace is $72K-$108K per year, which includes base salary and additional pay. The average Clinical Research Associate I base salary at Medpace is $83K per year. The average additional pay is $5K per year, which could include cash bonus, stock, commission, profit sharing or tips.

  4. Clinical Research Associate Salaries in the United States for Medpace

    $80,010 per year 12% Below national average Average $80,010 Low $28,000 High $158,000 Salary estimated from 25 employees, users, and past and present job advertisements on Indeed in the past 12 months. Last updated: January 10, 2024 Compare all Clinical Research Associate salaries in the United States Common benefits at Medpace

  5. Clinical Research Associate (CRA) Salary at Medpace, Inc. in 2023

    $44k MEDIAN $56k 90% $88k The average salary for a Clinical Research Associate (CRA) is $56,415 in 2023 Base Salary $44k - $88k Bonus $1k - $23k Total Pay $44k - $92k Based on 42 salary...

  6. MEDPACE Clinical Research Associate-Entry Level

    The average salary for Clinical Research Associate-Entry Level at companies like MEDPACE in the United States is $86,567 as of January 26, 2024, but the range typically falls between $74,919 and $98,214.

  7. Clinical Research Associate Medpace Salary: Hourly Rate

    A Clinical Research Associate Medpace in your area makes on average $41 per hour, or the same as the national average hourly salary of $41.13. Virginia ranks number 5 out of 50 states nationwide for Clinical Research Associate Medpace salaries. To estimate the most accurate hourly salary range for Clinical Research Associate Medpace jobs ...

  8. Medpace salaries: How much does Medpace pay?

    Clinical Research Associate $80,010 per year 25 salaries reported Clinical Trial Administrator $111,709 per year 13 salaries reported Statistical Analyst $86,762 per year 13 salaries reported Scientific Research & Development Scientist $89,090 per year

  9. Medpace Clinical Research Associate Job Description: Salary, Duties

    Medpace Clinical Research Associate Salary. The salary of a Clinical Research Associate at Medpace is determined by a variety of factors, including the individual's experience and qualifications, the complexity of the job, the geographic location of the position, and the company's budget. Additionally, the company may take into ...

  10. Clinical Research Associate Medpace jobs

    60 Clinical Research Associate Medpace jobs available on Indeed.com. Apply to Clinical Research Coordinator, Clinical Assistant, Clinical Research Associate and more!

  11. Medpace Clinical Research Associate Salaries

    Medpace Clinical Research Associate Salaries | Glassdoor See All Photos Medpace Engaged Employer Overview 1.2K 705 Jobs 2.8K Salaries 566 Interviews 293 Benefits 42 Photos 475 Diversity + Add a Salary Salary Details for a Clinical Research Associate at Medpace in Dallas-Fort Worth, TX Updated Oct 29, 2023 Any Location Argentina Australia Belgium

  12. MEDPACE Clinical Research Associate-Dallas Entry Level

    The average salary for Clinical Research Associate-Dallas Entry Level at companies like MEDPACE in the United States is $86,349 as of December 27, 2023, but the range typically falls between $74,731 and $97,966.

  13. Medpace hiring Clinical Research Associate

    The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the ...

  14. Clinical Research Associate (CRA)

    9494 Job Summary The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them.

  15. Clinical Research Organization Jobs

    Clinical Research Organization Jobs | Medpace When you want to work alongside some of the brightest minds in biotech, Medpace is where you belong. We support our clients to advance the development of treatments for diseases that impact millions — inspiring solutions that make our team, our communities, and our world better. Join us today.

  16. Clinical Research Associate yearly salaries in Ohio at Medpace

    Average Medpace Clinical Research Associate yearly pay in Ohio is approximately $83,461, which is 8% below the national average. Salary information comes from 164 data points collected directly from employees, users, and past and present job advertisements on Indeed in the past 36 months. Please note that all salary figures are approximations ...

  17. Medpace Associate Clinical Research Salaries

    758 Jobs 2.7K Salaries 571 Interviews 291 Benefits 42 Photos 461 Diversity + Add a Salary Salary Details for a Clinical Research Associate at Medpace Updated Oct 15, 2023 United States Argentina Australia Belgium Canada Czech Republic France Germany India Italy Netherlands Russia Singapore Spain United Kingdom United States Any Experience

  18. Clinical Research Associate

    9311 Job Summary Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team! This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace.

  19. Medpace Clinical Research Associate II Salaries

    $74K - $105K /yr $88K (Median Total Pay) The estimated total pay range for a Clinical Research Associate II at Medpace is $74K-$105K per year, which includes base salary and additional pay. The average Clinical Research Associate II base salary at Medpace is $83K per year.

  20. Clinical Research Coordinators

    Key Positions Clinical Research Coordinators Whether you're striving to make the transition into a CRA role, or wanting to develop your skills in new area, our Clinical Operations department has a position for you! Clinical Research Associate Clinical Trial Manager Data Coordinator Patient Recruitment Coordinator Project Coordinator

  21. Nursing in Clinical Research: Cody McClanahan Pulls Back the Curtain

    Nursing in Clinical Research: Cody McClanahan Pulls Back the Curtain. May 12, 2023. "To put it simply, I wanted to help people," says Clinical Research Associate (CRA) Manager Cody McClanahan, RN, BSN. Today, Cody is a CRA Manager at Medpace, but he actually began his career as a nurse caring for patients at a hospital.

  22. Medpace Entry Level Clinical Research Associate Salaries

    Salary Details for a Clinical Research Associate (Entry Level) at Medpace Updated Oct 29, 2023 United States Spain United States Any Experience Any Experience 0-1 Years 1-3 Years 4-6 Years 7-9 Years 10-14 Years 15+ Years Confident Total Pay Range $50K - $77K / yr Base Pay $50K - $77K / yr $62K /yr

  23. Clinical Research Associate Salaries in Cincinnati, OH for Medpace

    Average Medpace Clinical Research Associate yearly pay in Cincinnati is approximately $86,267, which meets the national average. Salary information comes from 161 data points collected directly from employees, users, and past and present job advertisements on Indeed in the past 36 months. Please note that all salary figures are approximations ...

  24. Entry-Level Clinical Research Associate (Cincinnati, OH)

    Cincinnati, Ohio Clinical Research Associate 9290 Job Summary Join our team in Cincinnati, Ohio! The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them.

  25. Clinical Research Associate

    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 5,000 people across 40+ countries.