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- Tasks: Join our team to manage clinical trials and collaborate on global study activities.
- Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics.
- Benefits: Enjoy flexible work, competitive pay, professional growth opportunities, and wellness initiatives.
- Why this job: Kickstart your career with intensive training in a dynamic, impactful environment.
- Qualifications: PhD in Life Sciences required; no prior industry experience needed but advantageous.
- Other info: Be part of a company recognised as one of America's Most Successful Midsize Companies.
The predicted salary is between 36000 - 60000 £ per year.
Overview Medpace is currently seeking candidates with gastrointestinal related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a 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.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 managerEnsure timely delivery of recurrent tasks consistently with a high degree of accuracyCompile and maintain project-specific status reports within the clinical trial management systemInteract with the internal project team, Sponsor, study sites, and third-party vendorsProvide oversight and quality control of our internal regulatory filing systemProvide oversight and management of study suppliesCreate and maintain project timelinesCoordinate project meetings and produce quality minutesQualifications PhD in Life SciencesFluency in English with solid presentation skillsAbility to work in a fast-paced dynamic industry within an international teamPrior experience within the CRO or pharmaceutical industry not required but will be advantageousMedpace 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 environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesAwards Recognized by Forbes as one of America\\\’s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat To Expect Next A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Trial Manager (PhD) - Gastrointestinal
✨Tip Number 1
Network with professionals in the clinical trial management field. Attend industry conferences or webinars where you can meet people from Medpace or similar organisations. Building these connections can give you insights into the company culture and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest trends and technologies in clinical trial management. Being knowledgeable about current practices will not only boost your confidence but also demonstrate your commitment to the role during interviews.
✨Tip Number 3
Prepare to discuss how your PhD research can be applied to clinical project management. Think of specific examples where your analytical skills and academic experience can contribute to the responsibilities outlined in the job description.
✨Tip Number 4
Showcase your communication and collaboration skills. Since the role involves working closely with various teams, be ready to provide examples of how you've successfully worked in team settings or managed projects during your academic career.
We think you need these skills to ace Associate Clinical Trial Manager (PhD) - Gastrointestinal
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your PhD and any relevant research experience. Emphasise skills that align with clinical trial management, such as analytical abilities and project coordination.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your desire to transition into the industry. Mention specific experiences from your academic background that demonstrate your suitability for the role.
Highlight Relevant Skills: In your application, focus on skills that are crucial for the Associate Clinical Trial Manager position, such as communication, collaboration, and attention to detail. Provide examples of how you've used these skills in your previous work or research.
Prepare for Potential Interviews: While this step comes after your application, it's good to prepare by thinking about common interview questions related to clinical trial management. Be ready to discuss how your academic background can contribute to Medpace's mission.
How to prepare for a job interview at Medpace
✨Showcase Your Analytical Skills
As a candidate with a PhD, it's crucial to highlight your analytical and academic skills during the interview. Be prepared to discuss specific examples from your research that demonstrate your ability to analyse data and solve complex problems, as these skills are essential for the Associate Clinical Trial Manager role.
✨Understand Clinical Trial Management
Familiarise yourself with the basics of clinical trial management and the specific responsibilities of the role. Research Medpace's approach to clinical trials and be ready to discuss how your background can contribute to their mission of developing safe and effective therapeutics.
✨Prepare for Team Collaboration Questions
Since the role involves working closely with project coordinators and clinical trial managers, expect questions about teamwork and collaboration. Think of examples where you've successfully worked in a team setting, especially in an international or fast-paced environment, to illustrate your ability to communicate effectively.
✨Ask Insightful Questions
At the end of the interview, take the opportunity to ask thoughtful questions about the company culture, training programmes, and career progression within Medpace. This shows your genuine interest in the position and helps you assess if the company aligns with your career goals.
