Job Summary : Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we’re looking for experienced professionals to join us as we prepare to launch of our newest office in Hyderabad, India . This is more than just a job. It’s an opportunity to be part of something from the very beginning. You’ll play a direct role in shaping the culture, building the team, and influencing how we grow in India. From day one, your work will make a meaningful impact across global projects. Why Join Medpace in Hyderabad? Be a Founding Member : Help establish and lead operations at our newest location. Immediate Impact : Your experience will directly influence Medpace’s growth in the region. Career Growth : As the office grows, so will the leadership and advancement opportunities. Global Reach : Work on cutting-edge clinical trials with international teams and top-tier sponsors. Strong Culture : Join a company known for its stability and commitment to professional development. Support & Infrastructure : While the Hyderabad office is new, you’ll be backed by the global resources and processes of a well-established CRO. If you’re looking for a new challenge, and want to be part of building something meaningful while advancing your career with a company that’s investing in your region — we’d love to hear from you. Help shape the future of Medpace in Hyderabad. Apply today. Responsibilities : The primary role of the Project Manager is to provide tactical management, administration, and leadership to Medpace Core Laboratory’s project teams in order to ensure that the project proceeds on time and within budget; Manage complex studies with multiple modalities and/or primary endpoints related to MCL services. Experienced enough to propose and develop new strategies for overall project management and process improvement. Assists with business development activities such as capabilities presentations, development of scope of work, and bid defence presentations. Utilize study management tools to track: site start-up activities, site performance issues, submission of data, etc.; Responsible for the delivery of Medpace Core Laboratory services to sponsors within expected timelines and budget; Conducts ongoing study team meetings; Performs scheduling of activities and deliverables in conjunction with client and internal customers; Provides timely notification of all appropriate parties with deviations from timelines and/or deliverables; Conducts regular communication with team members, formal and informal, regarding study status or any other changes; Maintain ongoing Sponsor contact for project issues; serve as primary contact for Sponsor, internal project team and external vendors. Qualifications : Bachelor’s degree in life sciences and 5 years related pharmaceutical industry experience A thorough understanding of the clinical research process is required in order to provide leadership Ability to handle multiple projects, issues, and schedules concurrently Prior experience in Core Lab preferred. 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 imaging services are experiencing rapid growth, and we are currently looking for a full-time, office-based Imaging Technologist specializing in MRI or Nuclear Medicine to join our team in Mumbai, India. If you are seeking an exciting career where you can utilize your existing expertise and further enhance your professional growth, this opportunity is tailored for you. As an Imaging Technologist, your responsibilities will include performing quality assurance checks on medical imaging data to ensure compliance with protocol-specific requirements. You will be tasked with executing established image processing techniques across MRI or Nuclear medicine imaging modalities using both proprietary and third-party software. Additionally, you will be responsible for compiling and maintaining project-specific status reports and timelines associated with imaging studies, as well as carrying out project-specific tasks in adherence to Good Clinical Practices (GCP), regulatory requirements (21CFR Part 11), departmental SOPs, and project protocols. To qualify for this role, you should hold a Bachelor's Degree and be a graduate of an accredited school of Radiologic Technology or echocardiography program. Preference will be given to candidates with PET/CT, CNMT (Certified Nuclear Medicine Technologist), or ARRT - R certification. Ideally, you should possess 1-3 years of experience in clinical research or imaging-related fields, with a minimum of 2 years of experience as an Imaging Technologist in a hospital or imaging center. Previous experience in clinical trials or the pharmaceutical environment is considered advantageous. Medpace is a comprehensive clinical contract research organization (CRO) that offers Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our core mission is to expedite the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With headquarters in Cincinnati, Ohio, and a workforce of over 5,000 individuals spanning 40+ countries, we leverage local regulatory and therapeutic expertise across various key areas such as oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. At Medpace, we value People, Purpose, and Passion. Joining our team means making a difference tomorrow. We have positively impacted the lives of numerous patients and families dealing with various diseases over the past 30+ years, and the work we do today will continue to enhance the lives of individuals battling illness and disease in the future. Medpace offers a range of perks, including a flexible work environment, competitive compensation and benefits packages, structured career paths with opportunities for professional advancement, company-sponsored employee appreciation events, and initiatives promoting employee health and wellness. Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024, Medpace has also been consistently acknowledged with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility. If you are interested in this opportunity, a Medpace team member will review your qualifications and reach out with further details on the next steps. Medpace is an Equal Opportunity/Affirmative Action Employer committed to diversity in the workplace.,
The company's corporate activities are expanding rapidly, and we are currently looking for a full-time SAS Programmer to join our Biostatistics team in Mumbai, India. As a SAS Programmer, you will collaborate with a team to complete tasks vital to the company's success. If you are seeking a dynamic career where you can leverage your existing skills and further enhance your professional growth, this opportunity is tailor-made for you. Your responsibilities will include writing SAS programs to generate analysis datasets, tables, listings, and figures. You will program, validate, and manage mapped databases using SAS. Additionally, you will develop edit checks for external data and liaise with Data Management to address database specifications and data transfers efficiently. To qualify for this role, you should hold a Bachelor's or Master's Degree in math, Statistics, health informatics, data science, computer science, or a life sciences field. A SAS Certification is mandatory, and proficiency in SAS with 1 to 2 years of experience is preferred. Strong written and verbal communication skills in English are essential for this position. Medpace is a comprehensive clinical contract research organization that offers Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to expedite the global advancement of safe and effective medical therapeutics through a scientific and disciplined approach. With expertise in various therapeutic areas such as oncology, cardiology, metabolic disease, and more, we operate in over 40 countries with our headquarters in Cincinnati, Ohio, employing a diverse workforce of over 5,000 individuals. At Medpace, we value People, Purpose, and Passion. By joining our team, you can make a difference today that will positively impact the lives of patients and families dealing with a myriad of diseases. Our work is focused on improving the future well-being of individuals battling illness and disease. As part of the Medpace team, you can enjoy various perks such as a flexible work environment, competitive compensation and benefits package, generous PTO packages, structured career development opportunities, company-sponsored employee appreciation events, and health and wellness initiatives for employees. Medpace has been recognized by Forbes as one of America's Most Successful Midsize Companies from 2021 to 2024. We have also consistently received CRO Leadership Awards from Life Science Leader magazine for our expertise, quality, capabilities, reliability, and compatibility. If you are interested in joining our team, submit your qualifications, and a Medpace team member will review them. If your profile matches our requirements, you will be contacted with further details on the next steps in the recruitment process. Medpace is an Equal Opportunity/Affirmative Action Employer, providing equal employment opportunities to all individuals regardless of gender, disability, or veteran status.,
You are currently seeking a full-time, office-based Data Engineer to join the Information Technology team at our rapidly growing corporate activities. In this role, you will work collaboratively with a team on tasks and projects crucial to the company's success. If you are looking for a dynamic career opportunity to utilize your expertise and further develop and enhance your skills, this position is the perfect fit for you. Your responsibilities will include utilizing your skills in data warehousing, business intelligence, and databases such as Snowflake, ANSI SQL, SQL Server, and T-SQL. You will support programming/software development using ETL and ELT tools like dbt, Azure Data Factory, and SSIS. Designing, developing, enhancing, and supporting business intelligence systems primarily using Microsoft Power BI will be a key part of your role. Additionally, you will be responsible for collecting, analyzing, and documenting user requirements, participating in software validation processes, creating software applications following the software development lifecycle, and providing end-user support for applications. To qualify for this position, you should have a Bachelor's Degree in Computer Science, Data Science, or a related field, along with at least 3 years of experience in Data Engineering. Knowledge of developing dimensional data models, understanding of Star Schema and Snowflake schema designs, solid ETL development and reporting knowledge, and familiarity with Snowflake cloud data warehouse, Fivetran data integration, and dbt transformations are preferred. Proficiency in Python, REST API, SQL Server databases, and bonus knowledge of C#, Azure development is desired. Excellent analytical, written, and oral communication skills are essential for this role. Medpace is a full-service clinical contract research organization (CRO) dedicated to providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. With a mission to accelerate the global development of safe and effective medical therapeutics, Medpace leverages local regulatory and therapeutic expertise across various major areas. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 individuals across 40+ countries. At Medpace, you will be part of a team that makes a positive impact on the lives of patients and families facing various diseases. The work you do today will contribute to improving the lives of individuals living with illness and disease in the future. Medpace offers a flexible work environment, competitive compensation and benefits package, structured career paths for professional growth, company-sponsored employee appreciation events, and employee health and wellness initiatives. Medpace has been recognized by Forbes as one of America's Most Successful Midsize Companies and has received CRO Leadership Awards for expertise, quality, capabilities, reliability, and compatibility. If your qualifications align with the requirements of the position, a Medpace team member will review your profile, and if interested, you will be contacted with further details on the next steps. Join us at Medpace and be a part of a team driven by People, Purpose, and Passion to make a difference tomorrow.,
As an Entry Talent Acquisition Specialist at Medpace, you will play a crucial role in supporting the Talent Acquisition team in the Asia Pacific region from our Mumbai, India office. Your primary responsibility will involve assisting in the hiring process and contributing to talent acquisition efforts. You will spend a significant amount of time on tasks such as sourcing candidates, reviewing CVs, and coordinating hiring events and career fairs. To excel in this role, you must be highly motivated, possess excellent communication skills, and have a strong desire to learn about recruitment in a dynamic industry. Your key responsibilities will include: - Creating compelling and precise job advertisements for various positions to attract high-quality applicants - Establishing and nurturing relationships with candidates to ensure a positive recruitment experience - Screening and interviewing applicants efficiently to assess their skills and cultural fit - Collaborating with hiring managers to define job requirements and align on recruitment activities - Managing requisitions in the applicant tracking system and HRIS - Providing guidance to hiring managers on interview processes and best practices - Conducting market research to stay informed about industry trends and competitor practices - Ensuring compliance with local employment laws and regulations - Contributing to employer branding efforts to attract top talent - Coordinating the employment offer process and facilitating seamless onboarding for new hires - Continuously seeking opportunities to improve and streamline the recruitment process To be successful in this role, you should have a Bachelor's Degree, effective communication skills, attention to detail, the ability to work in a fast-paced environment, and basic knowledge of recruitment processes and tools. Additionally, you should be highly organized and capable of managing multiple tasks simultaneously. Medpace is a leading clinical research organization that offers Phase I-IV clinical development services to various industries. Headquartered in Cincinnati, Ohio, we operate in over 40 countries and are dedicated to accelerating the global development of safe and effective medical therapeutics. By joining our team, you will have the opportunity to make a real difference in the lives of patients and contribute to groundbreaking research in key therapeutic areas. At Medpace, we value our employees and offer a range of perks including a flexible work environment, competitive compensation and benefits, structured career paths, employee appreciation events, and health and wellness initiatives. Our commitment to excellence has been recognized by Forbes and Life Science Leader magazine, highlighting our success and industry leadership. If you are ready to take on this exciting opportunity to contribute to our global recruitment efforts and help shape the future of medical research, we encourage you to apply today. A member of the Medpace team will review your qualifications, and if there is a potential match, you will be contacted with further details on the next steps. Join us at Medpace and be part of a team that is dedicated to making a positive impact on the world of clinical research.,
The corporate activities are expanding rapidly, and we are currently looking for a full-time, office-based SAS Programmer to join our Biostatistics team in India, Mumbai. As a SAS Programmer, you will collaborate with a team to complete tasks and projects crucial to the company's success. If you are seeking a dynamic career where you can apply your existing skills and further enhance your professional journey, then this role presents an excellent opportunity for you. Your responsibilities in this role will include writing SAS programs to generate analysis datasets, tables, listings, and figures. You will be required to program, validate, and maintain mapped databases using SAS. Additionally, you will develop edit checks for external data and facilitate communication with Data Management regarding database specifications and data transfers. To qualify for this position, you should hold a Bachelor's or Master's Degree in math, Statistics, health informatics, data science, computer science, or a related life sciences field. A SAS Certification is mandatory, and familiarity with SAS is essential, with 1 to 2 years of experience preferred. Proficiency in written and verbal English communication is also a prerequisite. Medpace is a comprehensive clinical contract research organization (CRO) that delivers Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device sectors. Our mission is to hasten the global advancement of safe and effective medical treatments through a scientific and methodical approach. With expertise in various therapeutic areas such as oncology, cardiology, metabolic disease, and more, we operate globally with a workforce of over 5,000 employees in 40+ countries, headquartered in Cincinnati, Ohio. Joining Medpace offers you the opportunity to work with a team dedicated to making a difference. The impact of our work over the past three decades has been significant in improving the lives of numerous patients and families affected by various diseases. By collaborating with us, you will contribute to enhancing the well-being of individuals living with illnesses and diseases. Working at Medpace comes with several benefits, including a flexible work environment, competitive compensation and benefits package, generous PTO packages, structured career paths with room for professional growth, company-sponsored employee appreciation events, and initiatives promoting employee health and wellness. Medpace has been acknowledged by Forbes as one of America's Most Successful Midsize Companies from 2021 to 2024 and has consistently received CRO Leadership Awards from Life Science Leader magazine for expertise, quality, capabilities, reliability, and compatibility. If you are interested in this position, a Medpace team member will evaluate your qualifications and reach out to you with details on the next steps. Medpace is an Equal Opportunity/Affirmative Action Employer committed to diversity and inclusion.,
You will play a direct role in shaping the culture, building the team, and influencing how Medpace grows in India by joining as a professional in the newest office in Hyderabad. Your work will have a meaningful impact on global projects from day one. As a founding member, you will help establish and lead operations in Hyderabad, contributing to Medpace's growth in the region. There will be ample opportunities for career growth and advancement as the office expands. Working on cutting-edge clinical trials with international teams and esteemed sponsors will give you a global exposure. Despite being a new office, you will have the support of global resources and processes from a well-established Clinical Research Organization (CRO) like Medpace. Your responsibilities will include developing, programming, validating, and maintaining clinical trial databases according to company standards. You will also be tasked with maintaining and preparing data models, acting as the primary programmer contact to the data management team for assigned studies, providing necessary technical support, ensuring quality programming, and adhering to company standards. To qualify for this role, you should hold at least a Bachelor's degree, preferably in a math or information science field. Flexibility, ability to manage multiple priorities effectively, excellent verbal and written communication skills, and meticulous attention to detail are essential. Familiarity with programming languages like C# and SQL would be advantageous. Medpace, a full-service clinical contract research organization, offers Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, with a presence in over 40 countries and employing more than 5,000 people, Medpace aims to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. The company leverages local regulatory and therapeutic expertise across various areas such as oncology, cardiology, metabolic disease, endocrinology, anti-viral, and anti-infective. Medpace values people, purpose, and passion, aiming to make a positive difference tomorrow. The company's work over the past 30+ years has positively impacted the lives of numerous patients and families facing various diseases. By joining Medpace, you can contribute to improving the lives of individuals living with illness and disease in the future. In addition to a flexible work environment, Medpace offers a competitive compensation and benefits package, structured career paths with opportunities for professional growth, company-sponsored employee appreciation events, and employee health and wellness initiatives. The company has been recognized by Forbes as one of America's Most Successful Midsize Companies multiple times and has received CRO Leadership Awards from Life Science Leader magazine for expertise, quality, capabilities, reliability, and compatibility. If interested, a Medpace team member will review your qualifications and reach out to you with details for the next steps. Join Medpace today to be part of a dynamic team that is dedicated to advancing medical research and improving patient outcomes.,
As a Lead Software Engineer at our Mumbai office, you will play a key role in the modernization of aging applications and administrative systems. Your strong attention to detail, desire for process ownership, and interest in implementing new technology will be highly valued as you contribute to a new team within our fast-growing organization. You will have the opportunity to collect, analyze, and document user requirements, design, modify, develop, and support software applications, and participate in the software validation process. Your responsibilities will also include creating software applications by following the software development life-cycle, communicating with team members, and utilizing skills in areas such as object-oriented programming (C#), databases (SQL), and web applications (ASP.NET). Additionally, there will be potential opportunities for you to lead software development projects. To excel in this role, you should hold a Bachelor's Degree in Computer Science and have at least 8-12 years of software development experience using technologies such as C#, Angular, Webservices, GraphQL, Git, and relational databases. Experience in Entity Framework and Azure DevOps would be advantageous, along with an understanding of the software development life cycle and software release management. Prior experience in modernizing systems to a cloud-based platform (Azure) is a plus. Strong analytical, written, and oral communication skills in English are essential for success. Joining Medpace, a full-service clinical contract research organization, will allow you to be part of a mission to accelerate the global development of safe and effective medical therapeutics. With a focus on various therapeutic areas, including oncology, cardiology, metabolic disease, and more, you will contribute to positively impacting people's lives by developing new treatments and therapeutics. At Medpace, you will have the opportunity to work in a flexible environment with competitive compensation and benefits, including structured career paths for professional growth. Employee health and wellness initiatives, company-sponsored events, and a supportive work culture make Medpace a rewarding place to build your career. If you are looking to make a difference and be part of a team that positively impacts lives, Medpace offers a fulfilling environment where your contributions matter. Join us and be a part of our mission to improve the lives of patients and families facing various diseases across therapeutic areas.,
You are invited to join Medpace as an IT Infrastructure Manager for our Navi Mumbai and APAC team, as part of our expanding global corporate activities. In this role, you will play a crucial part in growing our IT footprint beyond the US and EU, by overseeing various IT teams in Mumbai that focus on Software Development, System Validation, Infrastructure, and IT Support. This is a unique opportunity to contribute to a new team within a fast-growing organization known for its custom software and robust infrastructure that drive success. Your efforts will directly impact the development of new treatments and therapeutics, positively influencing people's lives worldwide. As the IT Infrastructure Manager at Medpace, your key responsibilities will include managing the global IT infrastructure, which encompasses routers, firewalls, servers, storage systems, and more. You will also be in charge of the physical aspects of the global infrastructure, ensuring compliance with technology standards and Medpace procedures. Additionally, you will oversee backup, restore, and archive processes, act as a liaison to various teams when IT infrastructure is involved, research and implement enhancements to meet company objectives, supervise and develop IT staff, and troubleshoot technical issues related to the IT infrastructure. To qualify for this role, you should hold a Bachelor's degree in Information Systems or a related field, possess at least 5 years of experience in IT Infrastructure, have hands-on experience with Microsoft and CISCO equipment, and demonstrate project management skills in IT Infrastructure. Excellent communication skills, both written and oral, are essential, along with the ability to manage IT staff effectively. Knowledge of Azure technologies and experience in a clinical or regulated environment are considered advantageous. Medpace is a leading clinical contract research organization dedicated to accelerating the global development of safe and effective medical therapeutics. With a mission to improve patient outcomes across various therapeutic areas, including oncology, cardiology, metabolic disease, and more, we offer a dynamic work environment where your contributions truly make a difference. Join Medpace today to be part of a team that values people, purpose, and passion. Enjoy a flexible work environment, competitive compensation and benefits, structured career paths with growth opportunities, employee appreciation events, and health and wellness initiatives. Recognized for our success by Forbes and awarded for our expertise and quality in the industry, Medpace offers a rewarding and fulfilling career path for individuals committed to making a positive impact on healthcare. If you are interested in joining our team, a Medpace representative will review your qualifications and reach out to you with further details on the next steps. Make a difference tomorrow by joining us today at Medpace.,
As a rapidly growing global Clinical Research Organization (CRO), Medpace is excited to invite experienced professionals to join as we launch our newest office in Hyderabad, India. This is an opportunity to be part of something from the very beginning by shaping the culture, building the team, and influencing our growth in India. Your work will have a meaningful impact on global projects from day one. Joining Medpace in Hyderabad means being a Founding Member, leading operations at the newest location, and making an immediate impact that will directly influence our growth in the region. As the office expands, you can expect career growth opportunities and the chance to work on cutting-edge clinical trials with international teams and top-tier sponsors. At Medpace, you will be part of a company known for stability, commitment to professional development, and supported by global resources and processes despite the newness of the Hyderabad office. If you are seeking a new challenge and want to contribute to building something meaningful while advancing your career with a company that invests in your region, we would love to hear from you. Help shape the future of Medpace in Hyderabad by applying today. Responsibilities: - Develop, program, validate, and maintain clinical trial databases following company standards - Maintain and prepare data models like electronic CRFs and program editing checks - Serve as the primary programmer contact to the data management team for assigned studies, offering necessary technical support, ensuring programming quality, and adhering to company standards Qualifications: - Bachelor's degree required, preferably in a math or information science field - Flexibility and ability to manage multiple priorities concurrently - Strong verbal and written communication skills to collaborate with various team members - Attention to detail is crucial - Familiarity with programming languages such as C# and SQL is preferred Medpace Overview: Medpace is a full-service clinical CRO providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With expertise in various therapeutic areas, we are headquartered in Cincinnati, Ohio, and employ over 5,000 people across 40+ countries. Why Medpace: Join a team driven by People, Purpose, and Passion, making a difference tomorrow. Our work positively impacts the lives of patients and families facing various diseases across key therapeutic areas. At Medpace, you can expect a flexible work environment, competitive compensation and benefits, structured career paths, employee appreciation events, and health and wellness initiatives. 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 awarded 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 the next steps.,
As a Software Engineer at our fast-growing organization, you will play a crucial role in the modernization of aging applications and the development of new software applications. Your strong attention to detail, passion for process ownership, and interest in implementing new technology will be highly valued in our Information Technology team. In this role, you will have the opportunity to work on Administrative Systems, collaborate with a dynamic team, and contribute to shaping the future of our organization. Your work will have a direct impact on people's lives as you participate in the development of new treatments and therapeutics. Your responsibilities will include collecting, analyzing, and documenting user requirements, designing, modifying, developing, and supporting software applications. You will also participate in the software validation process, create software applications following the software development life cycle, and communicate effectively with team members. Additionally, you will utilize your skills in areas such as object-oriented programming (C#), databases (SQL), and web applications (ASP.NET), with potential opportunities to lead software development projects. To excel in this role, you should possess a Bachelor's Degree in Computer Science, along with at least 2 years of software development experience using technologies like C#, Angular, Webservices, GraphQL, Git, and relational databases. Experience in Entity Framework and Azure DevOps is advantageous, and familiarity with the software development life cycle and software release management is essential. Prior experience in modernizing systems to a cloud-based platform (Azure) is a plus, and excellent analytical, written, and oral communication skills in English are required. Medpace is a full-service clinical contract research organization (CRO) dedicated to accelerating the global development of safe and effective medical therapeutics. Our mission is to positively impact patients" lives through scientific and disciplined approaches. With headquarters in Cincinnati, US, and a presence in over 40 countries, we offer a collaborative and rewarding work environment. At Medpace, we value people, purpose, and passion. By joining our team, you will have the opportunity to make a real difference in the world of healthcare. We offer a flexible work environment, competitive compensation and benefits packages, structured career paths, employee appreciation events, and health and wellness initiatives. Recognized by Forbes as one of America's Most Successful Midsize Companies and honored with CRO Leadership Awards, Medpace is committed to excellence and innovation in clinical research. If you are interested in joining us, a Medpace team member will review your qualifications and reach out with details for the next steps. Join us today and be part of a team that is dedicated to improving the lives of patients worldwide.,
Job Summary : Our imaging services are growing rapidly, and we are currently seeking a full-time, office-based Medical Physicist to join our team in Mumbai. If you want an exciting career where you will use your previous education and expertise to develop and grow your career even further, then this is the opportunity for you. You will work as part the Medpace Imaging Core Laboratory team. Responsibilities : Advice and review relating to radiation dosimetry and nuclear imaging on clinical trial protocols proposed by sponsors Design of imaging and dosimetry measures for use with diagnostic or therapeutic radionuclides Perform quality assurance checks on nuclear imaging and dosimetry data to ensure protocol specific requirements are met Scanner calibration by the analysis of phantom scans and calculation of the dosimetry conversion factor Image reconstruction and analysis (PET/CT, SPECT/CT and/or planar nuclear imaging) Dosimetry calculation (%ID/g, biological half-life, TIAC, estimated dose) in normal organ and tumor tissues using off the shelf and proprietary software Ensure compliance with MIRC and ICRP guidelines for radiation safety protection Compile and maintain project-specific status reports and project timelines associated with imaging components of clinical trials Perform project specific tasks in compliance with Good Clinical Practices (GCP), regulatory requirements (21CFR Part 11), applicable departmental and companywide SOPs, and project specific protocols. Qualifications : PhD or Master degree in physics or in other relevant field with at least 5 years’ experience in dosimetry calculation for internal radiotherapy (PRRT) Or PhD degree in physics or in other relevant field with at least 2 years’ experience in dosimetry calculation for internal radiotherapy (PRRT) Expertise in quantitative image reconstruction (nuclear medicine images) Expertise in internal radiotherapy and dosimetry calculation using MIRD S-values, 3D-RD and/or OLINDA/EXM 1.0 software Experience with internal radiation dosimetry for gamma, positron and alpha emitting radionuclides would be favored Experience working with clinical trials or within the pharmaceutical environment is preferred. Compensation A target salary range of $90,000-$150,000/year, dependent. Your compensation will be based on your skills and experience. Medpace offers the following benefits for eligible positions: medical, dental, vision, 401(k), vacation policy, sick days, paid holidays, work from home flexibility, short-term disability, long-term disability, health savings and flexible savings accounts, life and AD&D insurance, and pet insurance. For more details, please discuss with your recruiter. 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.
Job Summary : Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we’re looking for experienced professionals to join us as we prepare to launch of our newest office in Hyderabad, India . This is more than just a job. It’s an opportunity to be part of something from the very beginning. You’ll play a direct role in shaping the culture, building the team, and influencing how we grow in India. From day one, your work will make a meaningful impact across global projects. Why Join Medpace in Hyderabad? Be a Founding Member : Help establish and lead operations at our newest location. Immediate Impact : Your experience will directly influence Medpace’s growth in the region. Career Growth : As the office grows, so will the leadership and advancement opportunities. Global Reach : Work on cutting-edge clinical trials with international teams and top-tier sponsors. Strong Culture : Join a company known for its stability and commitment to professional development. Support & Infrastructure : While the Hyderabad office is new, you’ll be backed by the global resources and processes of a well-established CRO. If you’re looking for a new challenge, and want to be part of building something meaningful while advancing your career with a company that’s investing in your region — we’d love to hear from you. Help shape the future of Medpace in Hyderabad. Apply today. Responsibilities : Collect, analyze and document user requirements; Design, modify, develop and support software applications; Participate in software validation process through development, review, and/or execution of test plan/cases/scripts; Create software applications by following software development life-cycle, which includes requirements gathering, design, development, testing, release, and maintenance; Communicate with team members regarding projects, development, tools, and procedures; Utilize skills in development areas including object oriented programming (C#), databases (SQL) web applications (ASP.NET); and Potential opportunities to lead software development projects. Qualifications : Bachelor's Degree in Computer Science; Familiarity of technologies such as C#, Angular, Webservices, Git, relational databases; Experience in Entity Framework, Azure DevOps is advantageous; Understanding of software development life cycle (SDLC) and software release management; Prior experience modernizing systems to a cloud-based platform (Azure) is a plus; Excellent analytical, written and oral communication skills in English; and Prior experience developing mobile application (iOS/Android) is 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. EO/AA Employer M/F/Disability/Vets
As a Clinical Research (CRA) Manager at Medpace, you will play a crucial role in the clinical trial management process within our growing clinical operations team in Navi Mumbai, India. Your responsibilities will include line management of Clinical Research Associates (CRAs), overseeing recruitment, training, and development of CRAs, ensuring CRAs meet core monitoring responsibilities, managing CRA resourcing and allocation, as well as addressing turnover and retention to align with company objectives. To excel in this role, you should hold a Bachelor's degree with 4-6 years of experience in the pharmaceutical industry, specifically in clinical monitoring or study management. Ideally, you should have spent at least 3 years as a CRA and 1-2 years as a CRA Manager. Advanced knowledge of Good Clinical Practice is essential, along with strong leadership, mentoring, and communication skills. Proficiency in Microsoft Office software is required, and occasional travel for evaluating CRAs is expected (approximately 10% of the time). Medpace is a renowned full-service clinical contract research organization dedicated to accelerating the global development of safe and effective medical therapeutics. With expertise in various therapeutic areas such as oncology, cardiology, and central nervous system disorders, we operate in over 40 countries with a team of over 5,000 professionals. At Medpace, you will find a supportive work environment that values People, Purpose, and Passion. We offer competitive compensation and benefits packages, flexible work arrangements, structured career paths for professional growth, and employee appreciation events. Our commitment to employee health and wellness initiatives underscores our dedication to creating a positive workplace culture. Join us at Medpace and be part of a team that has been recognized by Forbes as one of America's Most Successful Midsize Companies multiple times. Our continuous receipt of CRO Leadership Awards speaks to our expertise, quality, reliability, and compatibility in the industry. If you are looking to make a real difference in the field of healthcare and contribute to improving the lives of patients worldwide, submit your qualifications for review. A member of the Medpace team will reach out if there is interest in moving forward with the next steps.,
Job Summary : Medpace, a rapidly growing global Clinical Research Organization (CRO), is excited to announce that we’re looking for experienced professionals to join us as we prepare to launch of our newest office in Hyderabad, India . This is more than just a job. It’s an opportunity to be part of something from the very beginning. You’ll play a direct role in shaping the culture, building the team, and influencing how we grow in India. From day one, your work will make a meaningful impact across global projects. Why Join Medpace in Hyderabad? Be a Founding Member : Help establish and lead operations at our newest location. Immediate Impact : Your experience will directly influence Medpace’s growth in the region. Career Growth : As the office grows, so will the leadership and advancement opportunities. Global Reach : Work on cutting-edge clinical trials with international teams and top-tier sponsors. Strong Culture : Join a company known for its stability and commitment to professional development. Support & Infrastructure : While the Hyderabad office is new, you’ll be backed by the global resources and processes of a well-established CRO. If you’re looking for a new challenge, and want to be part of building something meaningful while advancing your career with a company that’s investing in your region — we’d love to hear from you. Help shape the future of Medpace in Hyderabad. Apply today. Responsibilities : Responsibilities: Product Vision & Strategy: Develop and communicate a clear product vision and strategy for Core Lab’s solutions, aligning with Medpace's overall objectives. Product Development: Drive end-to-end project execution, including planning, sprint management, and release cycles. Requirements Gathering & Prioritization: Collaborate with radiologists, clinical trial sponsors, and internal stakeholders to gather user needs and translate them into detailed product requirements. Prioritize features based on impact, feasibility, and alignment with business goals. Agile Methodology: Utilize Agile methodologies to manage product development, ensuring iterative progress and timely delivery of features. Cross-functional Collaboration: Work closely with software engineering, quality assurance, regulatory affairs, and other teams to ensure successful product development and launch. Regulatory Compliance: Ensure all Core Lab solutions comply with relevant regulatory standards and quality procedures Stakeholder Management: Effectively communicate product updates and gather feedback from internal and external users. Qualifications : Bachelor's degree in Computer Science, or a related field. Good experience as a Product Manager in the health care domain is preferred. Proven track record of launching successful applications. Experience with Agile/Scrum methodologies and tools like JIRA, Confluence, or Azure DevOps. Excellent communication and stakeholder management skills. Ability to translate complex user needs into clear and actionable requirements. Nice-to-have Strong understanding of medical imaging technologies and workflows in clinical trials. Knowledge of regulatory standards and quality procedures for medical devices and software Experience with SQL databases, Angular, C#.NET 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. EO/AA Employer M/F/Disability/Vets
The clinical operations activities at our organization are expanding rapidly, and we are currently looking for a full-time Clinical Research (CRA) Manager to join our Clinical Monitoring team in Navi Mumbai, India. In this role, you will play a crucial part in the clinical trial management process at Medpace. If you are seeking a challenging career where you can utilize your existing expertise and further develop and advance your professional journey, then this opportunity is perfect for you. Your responsibilities will include: - Managing a team of Clinical Research Associates (CRAs) - Recruiting, providing initial and ongoing training, and fostering the development of CRAs - Overseeing and managing CRAs to ensure they fulfill their core monitoring responsibilities effectively - Tracking and managing CRA resourcing and assignment allocation - Handling turnover and retention of CRAs to align with company objectives To qualify for this position, you should have: - A Bachelor's degree with 4-6 years of experience in the pharmaceutical industry, specifically in clinical monitoring or study management, with at least 3 years as a CRA and 1-2 years as a CRA Manager preferred - Advanced knowledge of Good Clinical Practice - Strong leadership, mentoring, and motivational skills - Effective written and verbal communication abilities - Proficiency in Microsoft Office software - Willingness to travel occasionally for evaluating CRAs (approximately 10% of the time) Medpace is a comprehensive clinical contract research organization (CRO) that offers Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. Our mission is to expedite the global advancement of safe and effective medical therapeutics through a scientific and disciplined approach. With headquarters in Cincinnati, Ohio, we have a workforce of over 5,000 individuals spread across 40+ countries. At Medpace, we believe in People, Purpose, and Passion. By joining us, you can make a difference tomorrow. The work we have accomplished in the past three decades has positively impacted numerous patients and families dealing with various diseases across key therapeutic areas. The work we undertake today will enhance the lives of individuals living with illness and disease in the future. In addition to a fulfilling work environment, we offer: - Flexible work arrangements - Competitive compensation and benefits package - Generous PTO packages - Structured career paths with prospects for professional growth - Company-sponsored employee appreciation events - Employee health and wellness initiatives Medpace has been honored with several awards, including being recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024. We have also consistently received CRO Leadership Awards from Life Science Leader magazine, acknowledging our expertise, quality, capabilities, reliability, and compatibility. If you are interested in this opportunity, a Medpace team member will review your qualifications and reach out to you with further details on the next steps.,
You will be joining Medpace as a full-time Software QA Test Engineer (Validation Engineer) in the Mumbai office. Your main responsibility will be to collaborate with developers and end users to ensure that software applications meet user requirements throughout their life cycle. This will involve conducting various testing methodologies like manual, exploratory, and automated testing. In addition, you will be tasked with creating and maintaining test cases, test plans, and other project documentation. Your role will also include participating in peer reviews of test cases, identifying software defects, and ensuring comprehensive test coverage by reviewing and analyzing requirement specifications. Furthermore, you will assist in the execution of acceptance test scripts by end users. To qualify for this position, you must have a minimum of a Bachelor's degree and at least 1 year of experience in software testing, ideally in an agile-like environment. Proficiency in writing and executing manual tests for complex software applications is required, with experience in automated testing considered a bonus. Strong communication skills are essential as you will be working closely with cross-departmental teams comprising software developers, department leads, and end users. Additionally, a background in the regulated healthcare industry would be advantageous. Medpace is a leading clinical contract research organization offering Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries. The company is committed to accelerating the global development of safe and effective medical therapeutics by leveraging its scientific expertise and disciplined approach. With headquarters in Cincinnati, Ohio, and a presence in nearly 40 countries, Medpace employs over 5,000 professionals. Joining Medpace means becoming part of a team focused on driving positive change for patients worldwide. You will have the opportunity to work on impactful projects that contribute to the advancement of medical research and the improvement of patient outcomes. In addition to a flexible work environment, you can expect competitive compensation and benefits, generous PTO packages, structured career advancement opportunities, company-sponsored events, and employee health and wellness initiatives. Medpace has been recognized by Forbes as one of America's Most Successful Midsize Companies for multiple consecutive years, as well as receiving CRO Leadership Awards from Life Science Leader magazine for expertise, quality, capabilities, reliability, and compatibility. After submitting your application, a member of the Medpace team will review your qualifications. If your profile aligns with the requirements of the position, you will be contacted with further details on the next steps in the recruitment process.,
As a Project Coordinator at our Mumbai office, you will play a crucial role in supporting the success of our global activities. Working alongside a dedicated team, you will be responsible for compiling and maintaining project-specific status reports and timelines for Imaging studies. Your role will also involve engaging in Quality Assurance and Process Improvement activities on a day-to-day basis, ensuring the smooth flow of operations. Additionally, you will be tasked with managing the inventory of imaging supplies for study sites and facilitating communication between study sites and internal associates. To excel in this role, you must hold a Bachelor's Degree, with a Master's in Biomedical Engineering or Biotechnology being highly preferred. Previous experience in Quality Assurance and handling Quality Audits is essential, while a background in research-related activities would be advantageous. Strong computer skills, exceptional organizational abilities, and effective communication capabilities are key attributes that will contribute to your success in this position. Medpace, our esteemed clinical contract research organization, is dedicated to accelerating the global development of safe and effective medical therapeutics. With a focus on Phase I-IV clinical development services for the biotechnology, pharmaceutical, and medical device industries, we are committed to making a positive impact on patients" lives. Our diverse expertise spans various therapeutic areas, including oncology, cardiology, metabolic disease, and central nervous system disorders, among others. Headquartered in Cincinnati, Ohio, we operate in over 40 countries, with a team of more than 5,000 professionals. At Medpace, we believe in the power of people, purpose, and passion to drive meaningful change. By joining our team, you will have the opportunity to contribute to groundbreaking research that transforms the lives of individuals affected by a wide range of diseases. Our commitment to employee well-being is reflected in our flexible work environment, competitive compensation and benefits package, generous PTO offerings, and structured career development pathways. We also organize company-sponsored events to show appreciation for our dedicated staff and promote employee health and wellness initiatives. Recognized by Forbes as one of America's Most Successful Midsize Companies multiple times, Medpace has consistently received accolades for our expertise, quality, and reliability in the clinical research industry. As we continue to grow and innovate, we invite talented individuals like you to be part of our dynamic team and contribute to our ongoing success. If you are interested in joining us on this exciting journey, a Medpace representative will review your qualifications and reach out to you with further details on the next steps. As an equal opportunity employer, we welcome individuals from diverse backgrounds to apply and be a part of our inclusive workforce dedicated to advancing medical research and improving patient outcomes.,
You will be joining our Clinical Operations team in India, Mumbai as a full-time office-based Experienced Study Start-up Submissions Coordinator. Your role will be crucial in accomplishing tasks and projects that are essential for the success of our company. If you are seeking a rewarding career where you can utilize your expertise and further develop and grow professionally, this opportunity is perfect for you. At Medpace, we foster a culture of expertise and empowerment, allowing our teams to leverage their unique talents and experiences to approach research and problem-solving assertively, thereby supporting our business partners effectively. Our employees embody our values and commitment to serving our clients, working diligently, meeting high expectations, and embracing challenges. In return, they receive engaging projects, opportunities for career advancement, and exposure to our international presence. These are some of the reasons why talented individuals choose to be part of the Medpace team. Your responsibilities will include: - Performing necessary activities within the country to activate investigative sites for clinical trials across all phases. - Preparing, reviewing, and submitting documents to Regulatory Agencies. - Communicating with global study teams and personnel to update them on study progress. - Identifying and mitigating risks related to site activations effectively. - Providing expertise and guidance to global study teams regarding ethics and regulatory submissions. - Reviewing and finalizing essential documents required for site activation. - Serving as the main contact for Ethical and Regulatory submission-related activities. - Engaging directly with investigative sites during the study start-up and activation process. - Ensuring that submissions comply with relevant regulations and guidance documents. - Advising sponsors on changing regulations and compliance requirements. - Tracking submissions and ensuring timely filing of documents. Qualifications required: - Bachelor's degree in a scientific field or equivalent education and experience. - Minimum of 4 years of relevant work experience at a CRO, Pharmaceutical Company, or investigative site. - Strong organizational and communication skills. - Proficiency in Microsoft Office, ICH-GCP guidelines, and regulatory guidelines. - Hands-on experience in preparing, reviewing, and submitting regulatory documentation to Ethics Committees and Regulatory Agencies, including responding to queries. - Proficiency in English language. About Medpace: Medpace is a full-service clinical contract research organization (CRO) offering 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 a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise in various major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. With headquarters in Cincinnati, Ohio, we have a workforce of over 5,000 employees spread across 40+ countries. Why Choose Medpace: At Medpace, we believe in People, Purpose, and Passion. We offer a flexible work environment, competitive compensation and benefits package, structured career paths for professional growth, company-sponsored employee appreciation events, and health and wellness initiatives for employees. Our work has been recognized by Forbes as one of America's Most Successful Midsize Companies and we have received numerous CRO Leadership Awards for expertise, quality, capabilities, reliability, and compatibility from Life Science Leader magazine. What to Expect Next: If your qualifications align with our requirements, a Medpace team member will review your profile and contact you with further details regarding the next steps in the process. Thank you for considering a career with us.,
As a SQL Database Administrator at our rapidly growing corporate, you will be an integral part of the Information Technology team. Your primary responsibility will be to manage and secure the databases used by our critical enterprise applications. Working closely with Software Development teams, System Owners, and Business Owners, you will ensure that database solutions are optimized for performance, regularly updated, appropriately backed up, and aligned with compliance objectives. The ideal candidate for this role will possess extensive knowledge in database management, a strong background in MSSQL Database Solutions, and a forward-looking approach towards cloud-based database solutions. Your key responsibilities will include managing and optimizing the performance of databases for our critical systems, overseeing backup, restore, and archive procedures of database servers, and upgrading/installing database-related clustered and stand-alone servers in physical and virtual environments. Additionally, you will monitor SQL environments for health and performance, ensure the security and data integrity of all database environments, and troubleshoot and resolve any database-related issues that may arise. To qualify for this role, you should hold a Bachelor's degree in Information Systems or an equivalent field, have at least 5 years of experience in database administration, and demonstrate a thorough understanding of all features in current versions of Microsoft SQL Server. Experience with cloud-based technologies and Oracle is preferred, along with knowledge of database design and performance tuning. Familiarity with HADR (High Availability / Disaster Recovery), always On, and Failover Clusters will be beneficial. Medpace, a full-service clinical contract research organization, is dedicated to accelerating the global development of safe and effective medical therapeutics through a scientific and disciplined approach. With headquarters in Cincinnati, Ohio, and a presence in over 40 countries with more than 5,000 employees, we specialize in Phase I-IV clinical development services for the biotechnology, pharmaceutical, and medical device industries. Joining Medpace means being part of a team that is driven by People, Purpose, and Passion to make a Difference Tomorrow. Our work has positively impacted the lives of countless patients and families facing various diseases across key therapeutic areas. We offer a flexible work environment, competitive compensation and benefits packages, structured career paths with opportunities for professional growth, company-sponsored employee appreciation events, and employee health and wellness initiatives. Recognized by Forbes as one of America's Most Successful Midsize Companies in multiple years and consistently awarded CRO Leadership Awards from Life Science Leader magazine, Medpace is committed to excellence in expertise, quality, capabilities, reliability, and compatibility. If you are interested in joining our team, a Medpace representative will review your qualifications and reach out to you with details on the next steps. Make a meaningful impact on the future of healthcare by becoming a part of Medpace today.,