Singapore, Singapore · On-site
Medpace is delighted to host a Recruitment Event tailored to candidates studying or holding a PhD in Life Sciences. If you are looking for a transition to the Clinical Trial Industry, this is a perfect chance for your to…
Skills: Clinical Trial Management, Project Coordination, Stakeholder Management, Quality Control, Regulatory Filing
Leuven, Flemish Brabant, Belgium · On-site
We are seeking an Entry-level Sales Associate to join our Business Development team in Europe. This position works closely with internal Business Development Executives and is responsible for communicating both the scien…
Skills: Prospecting, Lead Generation, Market Research, Salesforce, Communication Skills
Lyon, Auvergne-Rhone-Alpes, France · On-site
We are seeking an Entry-level Sales Associate to join our Business Development team in Europe. This position works closely with internal Business Development Executives and is responsible for communicating both the scien…
Skills: Prospecting, Lead generation, Salesforce, Market research, Communication skills
City of London, England, United Kingdom · On-site
We are seeking an Entry-level Sales Associate to join our Business Development team in Europe. This position works closely with internal Business Development Executives and is responsible for communicating both the scien…
Skills: Prospecting, Lead Generation, Salesforce, Market Research, Communication Skills
City of London, England, United Kingdom · On-site
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Data Engineer to join our Information Technology team. This position will work on a team to accomplish tasks and projec…
Skills: Snowflake, ANSI SQL, SQL Server, T-SQL, dbt
United States · Remote OK
Medpace will be hosting a Virtual Networking Event to highlight our exciting Clinical Research Associate opportunites! We are seeking qualified Clinical Research Coordinators and Research Nurses to attend. When: Thursday…
Skills: Clinical Monitoring, Site Qualification, Case Report Form Verification, GCP Compliance, Regulatory Document Review
City of London, England, United Kingdom · On-site
Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team in London. This is a fantastic opportunity t…
Skills: Clinical Trial Management, Site Relationship Management, Feasibility Assessments, GCP Guidelines, Study Start-up
South Yarra, Victoria, Australia · On-site
Medpace is continuing to expand our global Clinical Trial Management team and is seeking an experienced Director, Clinical Trial Management (office base) to lead complex global clinical trials while developing and mentor…
Skills: Clinical Trial Management, Project Management, People Leadership, Operational Execution, Risk Assessment
City of London, England, United Kingdom · On-site
Computer Science or Data Science graduates, considering a career in the clinical trial industry? Medpace is delighted to host a recruitment event tailored to individuals interested in joining the Data Engineering team at…
Skills: Python, SQL, Snowflake, Azure, ETL
City of London, England, United Kingdom · On-site
Informatics or Computer Science graduate, considering a career in the clinical trial industry? Medpace is delighted to host a recruitment event tailored to individuals interested in joining the Clinical Informatics team …
Skills: R, Python, Shiny, Streamlit, PowerBI
City of London, England, United Kingdom · On-site
Medpace is delighted to host a Recruitment Event tailored to candidates studying or holding a PhD in Life Science. This is a rare and exciting opportunity for individuals seeking to make a switch from academia to the Cli…
Skills: Clinical Trial Management, Project Administration, Analytical Skills, Regulatory Filing, Project Timeline Management
Denver, Colorado, United States · Hybrid
Our Site Contracts team is growing, and we are seeking experienced individuals to join our Denver team as a full-time Contract Specialist. This role plays a key role in the study start-up and clinical trial management pr…
Skills: Contract Negotiation, Clinical Trial Management, Budget Negotiation, Risk Identification, Time Management
Cincinnati, Ohio, United States · On-site
Medpace is currently seeking candidates with a PhD in Life Sciences with a focus in Hematology and/or Oncology research for a full-time, office-based Medical Writer position. The Medical Writer will lead development of v…
Skills: Medical Writing, Clinical Study Reports, Protocol Development, Investigator's Brochures, IND Modules
Cincinnati, Ohio, United States · On-site
Medpace is currently seeking candidates with a PhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research for a full-time, office-based Medical Writer position. The Medical Writer will lead development…
Skills: Medical Writing, Clinical Study Reports, Protocol Development, Investigator's Brochures, IND Modules
City of London, England, United Kingdom · On-site
Medpace is delighted to host a Recruitment Event tailored to candidates with a Bachelor of Medicine, Bachelor of Surgery qualification. This is a rare and exciting opportunity for Medical Doctors to make a switch to the …
Skills: Clinical Trial Management, Project Administration, Regulatory Filing, Quality Control, Project Timeline Management
Cincinnati, Ohio, United States · On-site
Medpace is a rapidly growing global Contract Research Organization headquartered in Cincinnati and is seeking a Scientific and Technical Liaison for Medpace Reference Laboratories (MRL). This position is responsible for …
Skills: Technical review, Scientific review, Project management, Laboratory operations, Communication skills
Cincinnati, Ohio, United States · On-site
The Medpace Finance & Accounting Internship Program is a flexible, paid professional development opportunity that offers hands-on finance and accounting experience. Internships are in-person and will vary in scope by dep…
Skills: Financial Analysis, Forecasting, Valuation, Financial Modeling, Budgeting
Navi Mumbai, Maharashtra, India · On-site
Medpace is hosting a career info-session to share more about our SAS Programmer career within India. If you are a Life Science/ Biostatistics fresh graduate or junior clinical research professional looking to grow your c…
Skills: SAS Programming, Clinical SAS Programming, Data Validation, Database Mapping, Edit Checks
Navi Mumbai, Maharashtra, India · On-site
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based IRT Validator to join our Randomization and Study Product Management team in Mumbai, India. This position pla…
Skills: Test Plan Creation, Test Execution, Validation Packaging, Requirement Specification Review, Clinical Trial Management
Navi Mumbai, Maharashtra, India · On-site
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based RSP (Randomization & Study Product) Coordinator to join our team in India. By working with the other RSPM team members,…
Skills: Randomization & Study Product Management, Study Product Management, System Design, Client Requirement Gathering, Documentation
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The Associate Clinical Trial Manager collaborates with internal and external stakeholders to ensure the seamless execution of global clinical trials. Key duties include maintaining project status reports, managing study supplies, and coordinating project meetings.
A PhD in Life Sciences is required, with a background in key therapeutic areas such as Oncology or Cardiovascular being an advantage. Candidates must be fluent in English and capable of working in a fast-paced, international environment.
Medpace is delighted to host a Recruitment Event tailored to candidates studying or holding a PhD in Life Sciences. If you are looking for a transition to the Clinical Trial Industry, this is a perfect chance for your to explore a career in our Clinical Trial Management team. The Associate Clinical Trial Manager role in Medpace offers the unique opportunity in the research of drug and medical device development to accelerate the development of safe and effective medical therapeutics. Meet Medpace current employees and the management face-to-face, and discover the potential opportunities we have!
LOCATION: Medpace Singapore Office
DATE: 23 July 2026, Thursday
APPLICATION CLOSE DATE: 15 July 2026, Wednesday
As an aCTM, you will become an integral part of the operational teams for global clinical trials, collaborating with key internal stakeholders - Project Coordinators, Clinical Research Associates, Medical Monitors - and external stakeholders - Sponsors, Clinical Sites and Vendors - to ensure the seamless execution of studies.
This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the reserach and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).
What to Expect Next:
A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an RSVP.
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.
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
Awards
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
