Cincinnati, Ohio, United States · Remote OK
We are growing rapidly, and currently seeking a full-time, office or remote-based Site Contract Manager to join our Clinical Operations team (CRO experience required for remote-based). This position will work on a team t…
Skills: Clinical Trial Agreement (CTA) Management, Contract Negotiation, Budget Negotiation, Clinical Research Organization (CRO) Experience, Stakeholder Management
China · Remote OK
Our clinical activities are growing rapidly, and we are currently seeking a full-time, home-based Clinical Research Associate to join our Clinical Operations team in China. If you want an exciting career where you use yo…
Skills: Clinical Monitoring, Source Document Verification, Case Report Form Review, Regulatory Document Review, Drug Inventory Management
Taipei, Taipei, Taiwan · On-site
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Project Assistant to join our Clinical Safety team. This position will work on a team to accomplish tasks and projects …
Skills: Project Coordination, Clinical Safety Knowledge, English Fluency, Mandarin Fluency, Microsoft Office
Cincinnati, Ohio, United States · On-site
Medpace Reference Laboratories is currently seeking Laboratory Receiving Assistants to work in our Sample Management/Biorepository Department. This individual will be responsible for basic administrative duties as well a…
Skills: Sample Processing, Data Entry, Sample Management, Logistics, Good Documentation Practices
City of London, England, United Kingdom · On-site
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Contract Specialist to join our Clinical Operations team. This position plays a key role in the study start-u…
Skills: Contract Negotiation, Budget Negotiation, Clinical Trial Management, Administrative Support, Communication Skills
Munich, Bavaria, Germany · Hybrid
This position is office based in Munich, Germany. What can Medpace offer you? Flexible working conditions – Hybrid working model and flexible working hoursCompetitive employee benefitsAnnual Merit increasesCasual D…
Skills: Line Management, Clinical Research, Recruitment, Training and Development, Resource Allocation
South Yarra, Victoria, Australia · On-site
We are currently seeking a full-time, office based Experienced Regulatory Submissions (Study Start up) Coordinator to join our Clinical Operations team in the Australia, Melbourne office. This role is a vital part of the…
Skills: Regulatory Submissions, TGA Applications, Medsafe Submissions, Clinical Trial Activation, ICH-GCP Guidelines
China · Remote OK
Our clinical activities are growing rapidly, and we are currently seeking a full-time, home-based Clinical Research Associate to join our Clinical Operations team in China. If you want an exciting career where you use yo…
Skills: Clinical Monitoring, Source Document Verification, Case Report Form Review, Regulatory Document Review, Drug Inventory Management
Singapore, Singapore · On-site
Our laboratory is growing rapidly and we are currently seeking a full-time Laboratory Assistant to join our team. This position will work with a team to accomplish tasks and projects that are instrumental to the company&…
Skills: Specimen Inspection, Data Entry, Inventory Management, Sample Shipment Coordination, Vendor Management
Cincinnati, Ohio, United States · On-site
The Medpace Analytics Business Intelligence team is quickly growing and needs support establishing and maintaining processes for strong governance of BI reports, Automated workflows, micro apps, and AI solutions. As a Ju…
Skills: Data Governance, Business Systems Analysis, Agile, Scrum, Process Control
Cincinnati, Ohio, United States · On-site
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Project Assistant to join our Clinical Safety team. This position will work on a team to accomplish tasks and projects …
Skills: Database Entry, Document Filing, Organizational Skills, Prioritization, Microsoft Office
City of London, England, United Kingdom · On-site
Do you have a passion for Artificial Intelligence (AI) and are looking to make a difference in how the latest clinical trials progress into the market? Are you pursuing a degree in data science and/or computer science wi…
Skills: Machine Learning, Large Language Models, Python, TensorFlow, PyTorch
Copenhagen, Capital Region of Denmark, Denmark · Hybrid
The Clinical Research Associate role 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 …
Skills: Clinical Monitoring, Regulatory Document Review, GCP Compliance, Medical Record Verification, Patient Recruitment
Denmark · Remote OK
Our clinical activities are growing rapidly, and we are currently seeking full-time, home-based Clinical Research Associates to join our Clinical Operations team in Denmark (candidates can be based anywhere in Denmark). …
Skills: Clinical Monitoring, Source Document Verification, Case Report Form Review, Regulatory Document Review, Study Drug Inventory
Cincinnati, Ohio, United States · Hybrid
The Compensation Analyst is a critical role at Medpace, responsible for supporting complex compensation projects and serving as a compensation representative for global leaders within HR and operations. You will be part …
Skills: Compensation Analysis, Salary Surveys, Market Intelligence, Microsoft Excel, Microsoft Power BI
South Yarra, Victoria, Australia · On-site
We are currently seeking a full-time, office based Entry level Regulatory Submissions (Study Start up) Coordinator to join our Clinical Operations team in the Australia, Melbourne office. This role is a vital part of the…
Skills: Regulatory Submissions, TGA Applications, Medsafe Submissions, ICH-GCP Guidelines, Clinical Trial Activation
Stirling, Scotland, United Kingdom · On-site
Our Safety activities are growing rapidly, and we are currently seeking a full-time, Clinical Safety Coordinator to join our team in Stirling, Scotland. This position plays a key role in the pharmacovigilance process at …
Skills: Pharmacovigilance, Quality Control, Microsoft Office Suite, Good Clinical Practice (GCP), Medical Terminology
Navi Mumbai, Maharashtra, India · On-site
Medpace is growing rapidly, and we are currently seeking full-time, Junior Software QA Test Engineers (Validation Engineer) to join our growing Information Technology (IT) team in Mumbai office. Responsibilities Work clo…
Skills: Manual Testing, Automated Testing, Exploratory Testing, Test Case Creation, Test Planning
Cincinnati, Ohio, United States · On-site
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Entry Level Project Coordinator to join our Internal Data Monitoring team. This position will work on a team to accompl…
Skills: Administrative support, Logistical coordination, Meeting scheduling, Document maintenance, Written communication
Leuven, Flemish Brabant, Belgium · On-site
Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Office Assistant to join our team. If you want an exciting career where you use your previous expertise and can develop an…
Skills: Office Management, Reception, Facilities Management, Invoice Processing, Health And Safety
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The role involves end-to-end management of the clinical trial agreement process for global multi-site trials. Key duties include developing CTA strategies, creating country-specific templates, and negotiating budgets directly with sites.
Candidates must have a bachelor's degree in a legal or business field and over 8 years of direct Clinical CRO experience. Additionally, at least 4 years of management or oversight experience and proficiency in Microsoft Office are required.
We are growing rapidly, and currently seeking a full-time, office or remote-based Site Contract Manager to join our Clinical Operations team (CRO experience required for remote-based). 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!
Travel: minimal
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.
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
Collaborative Culture
Continuous Growth & Development
Other Employee Benefits
Cincinnati Headquarters Experience
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.
Accelerating Drug, Biologic and Medical Device Clinical Development
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 6,300 people across 46 countries.
Offices: 5375 Medpace Way, Cincinnati, OH 45227, US
Accelerating Drug, Biologic and Medical Device Clinical Development
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 6,300 people across 46 countries.
Offices: 5375 Medpace Way, Cincinnati, OH 45227, US
