PhD Career Event: Clinical Trial Management – Medpace London
PhD Career Event: Clinical Trial Management – Medpace London

PhD Career Event: Clinical Trial Management – Medpace London

City of London Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join our team as an Associate Clinical Trial Manager, managing clinical trial activities.
  • Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics.
  • Benefits: Enjoy flexible work, competitive pay, and structured career growth opportunities.
  • Why this job: Make a real impact in healthcare while transitioning from academia to industry.
  • Qualifications: PhD in Life Sciences required; experience in oncology or cardiology is a plus.
  • Other info: Attend our recruitment event on 18th September 2024 in Central London!

The predicted salary is between 36000 - 60000 £ per year.

Job Summary

Medpace is delighted to host a Recruitment Event tailored to candidatesstudying 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 Clinical Trials Industry!

LOCATION: Central London

DATE: Thursday 18th September 2024

APPLICATION CLOSE DATE: Monday 14th September

Associate Clinical Trial Manager

At this event, Medpace is seeking to meet candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) role to join our global Clinical Operations team. The aCTM will be working closely 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 accelerate 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).

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an RSVP.

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
  • A background in one of our key therapeutic focus areas is of advantage, but not a must: Oncology, Cardiovascular, Endocrine/metabolic,Nuclear Medicine, or Radiopharmaceuticals
  • Fluency in English with solid presentation skills
  • Ability to work in a fast-paced dynamic industry within an international team

Medpace Overview

Medpace is a full-service clinical contract research organisation (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.

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PhD Career Event: Clinical Trial Management – Medpace London employer: Medpace

Medpace is an exceptional employer, offering a unique opportunity for PhD graduates to transition from academia to the dynamic field of Clinical Trial Management in the heart of Central London. With a strong commitment to employee growth, Medpace provides structured career paths, comprehensive training, and a supportive work culture that values flexibility and wellness, all while making a meaningful impact on global health through innovative research and development.
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Contact Detail:

Medpace Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land PhD Career Event: Clinical Trial Management – Medpace London

✨Tip Number 1

Network with professionals in the clinical trial management field. Attend industry events, webinars, or local meetups to connect with people who work at Medpace or similar organisations. This can give you insights into the role and potentially lead to referrals.

✨Tip Number 2

Prepare to discuss how your academic skills translate to the clinical trials industry. Think about specific examples from your PhD or post-doctoral research that demonstrate your analytical abilities and project management experience.

✨Tip Number 3

Familiarise yourself with the clinical trial process and key terminology. Understanding the basics of clinical operations will help you engage in meaningful conversations during the event and show your genuine interest in the field.

✨Tip Number 4

Follow up after the event with a thank-you email to the recruiters you meet. Express your appreciation for their time and reiterate your interest in the Associate Clinical Trial Manager position. This can help keep you on their radar as they review candidates.

We think you need these skills to ace PhD Career Event: Clinical Trial Management – Medpace London

Analytical Skills
Project Management
Communication Skills
Attention to Detail
Collaboration Skills
Regulatory Knowledge
Time Management
Problem-Solving Skills
Presentation Skills
Ability to Work in a Fast-Paced Environment
Quality Control
Report Compilation
Adaptability
Teamwork

Some tips for your application 🫡

Understand the Role: Before applying, make sure to thoroughly understand the Associate Clinical Trial Manager role. Familiarise yourself with the responsibilities and qualifications listed in the job description to tailor your application accordingly.

Highlight Relevant Experience: In your CV and cover letter, emphasise any relevant experience you have, particularly in project management or research. If you have worked on clinical trials or have experience in a related therapeutic area, be sure to mention it.

Craft a Strong Cover Letter: Write a compelling cover letter that explains your motivation for transitioning from academia to the clinical trials industry. Highlight your analytical skills and how they can benefit Medpace in managing clinical projects.

Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial in clinical trial management.

How to prepare for a job interview at Medpace

✨Understand the Clinical Trial Landscape

Familiarise yourself with the basics of clinical trial management and the specific role of an Associate Clinical Trial Manager. Knowing how your academic skills can translate into this industry will impress the interviewers.

✨Showcase Your Analytical Skills

Prepare to discuss how your PhD research has equipped you with strong analytical skills. Be ready to provide examples of how you've used these skills in project management or data analysis, as they are crucial for the role.

✨Demonstrate Team Collaboration

Since the role involves working closely with various teams, be prepared to share experiences where you successfully collaborated with others. Highlight any interdisciplinary projects or teamwork during your studies.

✨Ask Insightful Questions

Prepare thoughtful questions about Medpace's projects, culture, and training opportunities. This shows your genuine interest in the company and the role, and it helps you assess if it's the right fit for you.

PhD Career Event: Clinical Trial Management – Medpace London
Medpace
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  • PhD Career Event: Clinical Trial Management – Medpace London

    City of London
    Full-Time
    36000 - 60000 £ / year (est.)

    Application deadline: 2027-08-01

  • M

    Medpace

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