Medpace
Associate Clinical Trial Manager - PhD - Postdoctoral - Ophthalmology
Medpace, Irving, Texas, United States, 75084
Medpace is currently seeking candidates with
PhDs and/or Post-Doctoral Research experience
related to
Ophthalmology
for a full-time,
office-based
Associate Clinical Trial Manager (aCTM) position in our Dallas, TX office. The aCTM is part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
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 research 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).
Responsibilities
Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
Compile and maintain project-specific status reports within the clinical trial management system
Interact with the internal project team, Sponsor, study sites, and third-party vendors
Provide oversight and quality control of our internal regulatory filing system
Provide oversight and management of study supplies
Create and maintain project timelines
Coordinate project meetings and produce quality minutes
Qualifications
PhD in Life Sciences
Expertise related to
Ophthalmology
Ability to work in a fast-paced dynamic industry within an international team
Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
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.
Dallas Perks
Dallas Campus Overview
Flexible work environment
Competitive PTO packages, starting at 20+ days
Competitive compensation and benefits package
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Community involvement with nonprofit organizations
Structured career paths with opportunities for professional growth
Discounts on local sports games, fitness gyms and attractions
Modern, ecofriendly campus with an on-site fitness center
Free on-site parking
Outdoor seating and workspace
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.
PhD in Life Sciences
Expertise related to
Ophthalmology
Ability to work in a fast-paced dynamic industry within an international team
Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
Compile and maintain project-specific status reports within the clinical trial management system
Interact with the internal project team, Sponsor, study sites, and third-party vendors
Provide oversight and quality control of our internal regulatory filing system
Provide oversight and management of study supplies
Create and maintain project timelines
Coordinate project meetings and produce quality minutes
#J-18808-Ljbffr
PhDs and/or Post-Doctoral Research experience
related to
Ophthalmology
for a full-time,
office-based
Associate Clinical Trial Manager (aCTM) position in our Dallas, TX office. The aCTM is part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
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 research 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).
Responsibilities
Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
Compile and maintain project-specific status reports within the clinical trial management system
Interact with the internal project team, Sponsor, study sites, and third-party vendors
Provide oversight and quality control of our internal regulatory filing system
Provide oversight and management of study supplies
Create and maintain project timelines
Coordinate project meetings and produce quality minutes
Qualifications
PhD in Life Sciences
Expertise related to
Ophthalmology
Ability to work in a fast-paced dynamic industry within an international team
Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
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.
Dallas Perks
Dallas Campus Overview
Flexible work environment
Competitive PTO packages, starting at 20+ days
Competitive compensation and benefits package
Company-sponsored employee appreciation events
Employee health and wellness initiatives
Community involvement with nonprofit organizations
Structured career paths with opportunities for professional growth
Discounts on local sports games, fitness gyms and attractions
Modern, ecofriendly campus with an on-site fitness center
Free on-site parking
Outdoor seating and workspace
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.
PhD in Life Sciences
Expertise related to
Ophthalmology
Ability to work in a fast-paced dynamic industry within an international team
Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
Compile and maintain project-specific status reports within the clinical trial management system
Interact with the internal project team, Sponsor, study sites, and third-party vendors
Provide oversight and quality control of our internal regulatory filing system
Provide oversight and management of study supplies
Create and maintain project timelines
Coordinate project meetings and produce quality minutes
#J-18808-Ljbffr