Medpace, Inc.

Role Description Our clinical activities are growing rapidly, and we are currently seeking a full-time home-based Regulatory Submissions Coordinator. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. - Prepare, review, and file clinical trial applications to domestic regulatory agencies; - Prepare and submit responses to queries and amendments to clinical trial applications; - Ensure submissions comply with applicable regulations and guidance documents; - Advise sponsors and internal stakeholders on changing regulations and compliance requirements; - Track submissions and ensure timely filing of documents. Qualifications - Minimum Bachelor's degree in life sciences; - At least one year of work experience as a Regulatory Submissions Coordinator for European regulation (CTR); - Excellent organization and communication skills; - Knowledge of Microsoft® Office; - Hands-on experience preparing, reviewing, and submitting regulatory documentation; - Greek (mother tongue) and very good knowledge of English. Benefits - Flexible work environment; - Competitive compensation and benefits package; - Competitive PTO packages; - Structured career paths with opportunities for professional growth; - Company-sponsored employee appreciation events; - Employee health and wellness initiatives. Company Description 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.

Role Description 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. Responsibilities - Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol. - Communication with the medical site staff including coordinators, clinical research physicians and their site staff. - Verifying 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. - Assessing 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 - Must have a minimum of a university degree in a health or life science related field. - 1.5 years’ work experience as a CRA. - Oncology monitoring experience would be an advantage. - Willing to travel approximately 60-80% nationally. - Familiarity with Microsoft® Office. - Must be detail-oriented and efficient in time management. - Strong communication and presentation skills a plus. - Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities. - Excellent verbal - written communication skills and excellent negotiations skills in Spanish and English. - Excellent time management and organization skills. Benefits - Interesting projects, career advancement, and recognition and exposure to our international footprint. - Flexible working conditions – Opportunity to work from home and flexible working hours. - Competitive employee benefits. - Annual Merit increases. - Fast PACE® – Accelerated, tailored training program based on your experience. - Opportunity for cross-functional and CRA leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager. - Sign on bonus may be appropriate for qualifying candidates. Company Description 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 5,000 people across 40+ countries.

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 medical and/or health/life science interest and 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 varied backgrounds in medical and other science-related healthcare fields. Individuals who have succeeded in the CRA role include: - Nurses - Dieticians - Pharmacy Technicians - Pharmaceutical/Device Sales Representatives - Biotech Engineers - PhD/Pharm.D candidates - Health and Wellness Coordinators - Research Assistants. PACE – MEDPACE CRA TRAINING PROGRAM 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 Professionals Achieving CRA Excellence: - 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. UNEXPECTED REWARDS 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 Responsibilities - Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol; - Communication with the medical site staff including coordinators, clinical research physicians and their site staff; - Verifying 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; - Assessing 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; Health or life science related field preferred; - Willing to travel approximately 60-80% nationally; - Familiarity with Microsoft® Office; and - Strong communication and presentation skills a plus. Medpace Overview 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 5,000 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. Medpace Perks - Flexible work environment - Competitive compensation and benefits package - Competitive PTO packages - Structured career paths with opportunities for professional growth - Company-sponsored employee appreciation events - Employee health and wellness initiatives Awards - 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.

Our European activities are growing rapidly, and we are currently seeking a full-time, home-based Regulatory Submissions Coordinator & Contract Specialist (Dual role) to join our Clinical Operations team, in the country of Georgia. As a Regulatory Submissions Coordinator & Contract Specialist (Dual role) you will have the opportunity to work within Regulatory Submissions and contract negotiations, supporting our many projects. You will be a productive member of the team and will be mentored and supported as you develop your skills. Working directly with Regulatory Submissions Coordinators and Contract Specialists, you will gain valuable hands-on experience to enable you to develop a career in clinical research. Please note that this role is not US based and you must be located in the country of Georgia to be considered. Responsibilities - Prepare, review, and file initial clinical trial applications to regulatory authorities and Ethics committees in Georgia; - Prepare and submit responses to queries and amendments to clinical trial applications; - Ensure submissions comply with applicable regulations and guidance documents; - Advise team members on changing regulations and compliance requirements; - Maintain the Clinical Trial Management System and ensure timely filing of documents; - Collection of essential documents and preparation essential documents packages for drug release; - Drafting, reviewing, negotiating, and finalizing agreements, termination letters or other legal documents required for a clinical study; - Identify and assesses legal, financial, and operational risks and escalate to appropriate Contract Lead or Contract Manager; - Provide recommendations and alternative resolutions throughout negotiations using established escalation channels; - Coordinate with internal functional departments to ensure various site startup activities are aligned with contractual process and mutually agreed up timelines. Qualifications - A minimum of a Bachelor's degree is required (preferably in a Life Sciences field or Law); - Experience preparing, reviewing, and submitting regulatory documentation to Ethics Committees and Regulatory Agencies; including formulating responses to queries; - Relevant working experience at a CRO, Pharmaceutical Company, or an investigative site; - Knowledge of local regulatory guidelines and legislation; - Excellent organizational and prioritization skills; - Use to work independently with a proactive approach; - Knowledge of Microsoft Office; - Fluency in Georgian and English; and - Great attention to detail and excellent oral and written communication skills. We kindly ask to submit applications in English. Medpace Overview 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 5,000 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. Medpace Perks - Flexible work environment - Competitive compensation and benefits package - Competitive PTO packages - Structured career paths with opportunities for professional growth - Company-sponsored employee appreciation events - Employee health and wellness initiatives Awards - 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.

Our European activities are growing rapidly, and we are currently seeking a full-time, home-based Regulatory Submissions Coordinator & Contract Specialist (Dual role) to join our Clinical Operations team, in Serbia. As a Regulatory Submissions Coordinator & Contract Specialist (Dual role) you will have the opportunity to work within Regulatory Submissions and contract negotiations, supporting our many projects. You will be a productive member of the team and will be mentored and supported as you develop your skills. Working directly with Regulatory Submissions Coordinators and Contract Specialists, you will gain valuable hands-on experience to enable you to develop a career in clinical research. Responsibilities - Prepare, review, and file initial clinical trial applications to regulatory authorities and Ethics committees in Latvia; - Prepare and submit responses to queries and amendments to clinical trial applications; - Ensure submissions comply with applicable regulations and guidance documents; - Advise team members on changing regulations and compliance requirements; - Maintain the Clinical Trial Management System and ensure timely filing of documents; - Collection of essential documents and preparation essential documents packages for drug release; - Drafting, reviewing, negotiating, and finalizing agreements, termination letters or other legal documents required for a clinical study; - Identify and assesses legal, financial, and operational risks and escalate to appropriate Contract Lead or Contract Manager; - Provide recommendations and alternative resolutions throughout negotiations using established escalation channels; - Coordinate with internal functional departments to ensure various site startup activities are aligned with contractual process and mutually agreed up timelines. Qualifications - A minimum of a Bachelor's degree is required (preferably in a Life Sciences field or Law); - Experience preparing, reviewing, and submitting regulatory documentation to Ethics Committees and Regulatory Agencies; including formulating responses to queries; - Relevant working experience at a CRO, Pharmaceutical Company, or an investigative site; - Knowledge of local regulatory guidelines and legislation; - Excellent organizational and prioritization skills; - Use to work independently with a proactive approach; - Knowledge of Microsoft Office; - Fluency in Serbian and English; and - Great attention to detail and excellent oral and written communication skills. We kindly ask to submit applications in English. Medpace Overview 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 5,000 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. Medpace Perks - Flexible work environment - Competitive compensation and benefits package - Competitive PTO packages - Structured career paths with opportunities for professional growth - Company-sponsored employee appreciation events - Employee health and wellness initiatives Awards - 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.

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. Through our PACE® Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a competitive salary. Please note that this role is fully home based and we are looking for candidates who will be comfortable learning and developing under a remote program. PACE® – MEDPACE CRA TRAINING PROGRAM Through our PACE® Training Program, you will join other Professionals Achieving CRA Excellence: - 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. UNEXPECTED REWARDS 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: - Remote working; - 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; - CRA training program (PACE®); - Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts; - Opportunities to work with international team of CRAs. - Defined CRA promotion and growth ladder with potential for mentoring and management advancements 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 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; - Experience as a Clinical Research Coordinator (minimum 1 year); - Ability to travel 60-70% to locations nationwide is required; some visits may be conducted remotely; - 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. Medpace Overview 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 5,000 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. 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.

Medpace is growing quickly and we are seeking a Clinical Research Associate to join our team in Montreal Canada. We are an innovative, scientifically oriented mid-sized CRO that is focused on full-service project work. This is a home-based position in Montreal Canada. Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence and receive customized, expedited training, and efficient onboarding to familiarize experienced CRAs with Medpace systems. WE OFFER THE FOLLOWING - Competitive bonus plans including Resourcing Bonus (following training completion and successful assignment to studies) and Yearly Travel Incentives - Voluntary retirement scheme - Home office furniture allowance, mobile phone and hotspot for internet access anywhere - In-house travel agents, reimbursement for airline club and TSA pre-check - Customized 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 - National assignments with average of 2 protocols - In-house administrative support for all levels of CRAs - Opportunities to work with international team of CRAs - Low turnover rates for CRAs - No metric for minimum required days on site per month - Flexible work hours across days within a week - Opportunity for CRA leadership positions – Lead CRA, CRA Manager - Many additional perks unmatched by other CROs! Responsibilities - Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP; - Maintain ongoing site correspondence and site files; - Complete visit reports and maintaining study-related databases; - Oversight and interaction with clinical research sites; and - Review of patient charts and clinical research data. Qualifications - Bachelor’s degree in science from an accredited university; - At least 1 year as a Clinical Research Associate or Clinical Research Coordinator; - Bilingual in English and French; - Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ICH E-6 guidelines and per Part-C, Division 5 of the Health Canada Food and Drug regulations; - Excellent interpersonal, written and verbal communication skills in English and French; - Strong attention to detail and organization skills; - Highly motivated, independent, flexible; - Ability to travel between 60-80%; - Ability to prioritize workload to meet timelines across multiple studies; and - Proficient in Microsoft Office. Medpace Overview 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 5,000 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. Medpace Perks - Flexible work environment - Competitive compensation and benefits package - Competitive PTO packages - Structured career paths with opportunities for professional growth - Company-sponsored employee appreciation events - Employee health and wellness initiatives Awards - 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.

Our European clinical activities are growing rapidly, and we are currently seeking full-time, home-based Clinical Research Associates to join our Clinical Monitoring team, in the country of Georgia. This position will be instrumental in growing the team in Georgia and accomplishing tasks and projects that are vital to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. The Clinical Research Associate at Medpace is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivalled support to our customers. If you want an exciting career where you use your medical or health background and education, travel extensively and are instrumental in the clinical trials process, this could be the opportunity for you. Our successful Clinical Research Associates possess varied backgrounds in the medical and related healthcare fields. Individuals who have succeeded in the CRA role include Registered Nurses, Dieticians, Pharmacists, Faculty of Science Graduates and Research Assistants. An extensive training program provides the platform to carry out your duties effectively and confidently. Please note that this role is not US based and you must be located in the country of Georgia to be considered. Responsibilities - Conduct pre-study, initiation, monitoring, and closeout visits for research sites - Perform source document verification and case report form review - Perform regulatory document review - Conduct study drug inventory - Perform adverse event and serious adverse event reporting and follow-up; and - Assess patient recruitment and retention Qualifications - Minimum a Bachelor of science in health-related field, MD or equivalent - Minimum of 1 year independent CRA monitoring - Broad knowledge of medical terminology and clinical patient management - Basic knowledge of drug therapy techniques and clinical research methodologies - Comprehensive knowledge of Local Regulations and ICH GCP - Excellent oral and written communication skills - Fluency in Georgian and English - Great attention to detail - Must hold a valid driver’s license - We kindly ask to submit applications in English Medpace Overview 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. Medpace Perks - Flexible work environment - Competitive compensation and benefits package - Competitive PTO packages - Structured career paths with opportunities for professional growth - Company-sponsored employee appreciation events - Employee health and wellness initiatives Awards - Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, 2024 and 2025 - 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.