Associate Clinical Trial Manager (PhD) - Cardiovascular

Associate Clinical Trial Manager (PhD) - Cardiovascular

Full-Time 30000 - 40000 £ / year (est.) No working from home possible
Medpace, Inc.

At a Glance

  • Tasks: Manage clinical trials and collaborate with global teams on innovative cardiovascular research.
  • Company: Join Medpace, a leader in clinical trial management with a supportive culture.
  • Benefits: Enjoy flexible work, competitive pay, and structured career growth opportunities.
  • Other info: Dynamic international environment with a focus on employee wellness and appreciation.
  • Why this job: Kickstart your career in clinical research with hands-on training and real-world impact.
  • Qualifications: PhD in Life Sciences and strong communication skills required.

The predicted salary is between 30000 - 40000 £ per year.

Medpace is currently seeking candidates with Cardiovascular related PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London 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 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
  • Fluency in English with solid presentation skills
  • 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
Benefits
  • 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

Associate Clinical Trial Manager (PhD) - Cardiovascular employer: Medpace, Inc.

Medpace, Inc. is an excellent employer for those seeking a dynamic role as a Feasibility Data Visualization Analyst in London. With a flexible work environment, competitive compensation, and a strong focus on structured career development, employees are empowered to grow and thrive while collaborating closely with clinical operations and medical teams to enhance data strategies. This supportive culture fosters innovation and meaningful contributions to clinical research.

Medpace, Inc.

Contact Details:

Medpace, Inc. Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Associate Clinical Trial Manager (PhD) - Cardiovascular

Tip Number 1

Network like a pro! Reach out to professionals in the clinical trial management field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of cardiovascular research and clinical trial processes. We recommend practising common interview questions with a friend to boost your confidence and ensure you shine during the real deal.

Tip Number 3

Showcase your analytical skills! During interviews, share specific examples from your PhD or post-doctoral research that highlight your problem-solving abilities. We want to see how you can apply those skills in a clinical setting.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!

We think you need these skills to ace Associate Clinical Trial Manager (PhD) - Cardiovascular

Analytical Skills
Project Management
Communication Skills
Collaboration
Attention to Detail
Quality Control
Regulatory Knowledge

Some tips for your application 🫡

Tailor Your CV:Make sure your CV highlights your PhD and any relevant research experience. We want to see how your background fits with the Associate Clinical Trial Manager role, so don’t be shy about showcasing your skills!

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re excited about the role and how your analytical skills can contribute to our team. Keep it engaging and personal – we love to see your passion!

Showcase Your Communication Skills:Since the role involves collaboration with various teams, make sure to highlight any experiences where you’ve effectively communicated complex ideas. We value clear communication, so let us know how you excel in this area!

Apply Through Our Website:We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and you’ll be one step closer to joining our fantastic team at Medpace!

How to prepare for a job interview at Medpace, Inc.

Know Your Stuff

Make sure you brush up on your cardiovascular knowledge and any relevant research you've done during your PhD. Be ready to discuss how your academic experience can translate into the practical aspects of clinical trial management.

Show Your Team Spirit

Since this role involves a lot of collaboration, be prepared to share examples of how you've worked effectively in teams. Highlight your communication skills and how you can contribute to a dynamic international environment.

Be Organised

Demonstrate your ability to manage multiple tasks and timelines. Bring examples of how you've successfully juggled projects in the past, and be ready to discuss how you would approach project management in this role.

Ask Smart Questions

Prepare thoughtful questions about the company's clinical trial processes and the specific challenges they face. This shows your genuine interest in the role and helps you understand if it's the right fit for you.