Project Assistant - Clinical Safety & Pharmacovigilance (office based in London)
Project Assistant - Clinical Safety & Pharmacovigilance (office based in London)

Project Assistant - Clinical Safety & Pharmacovigilance (office based in London)

London Full-Time 28800 - 43200 £ / year (est.) No home office possible
Go Premium
M

At a Glance

  • Tasks: Support the Clinical Safety team with project management and case processing tasks.
  • 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 on patient lives while developing your skills in a supportive environment.
  • Qualifications: No degree required; administrative experience and attention to detail are key.
  • Other info: Join a company recognised by Forbes for its success and commitment to quality.

The predicted salary is between 28800 - 43200 £ per year.

Job Summary
Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Project Assistant to join our Clinical Safety & Pharmacovigilance team in London . This position will work on a team to accomplish tasks and projects that are instrumental to the company\’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities

  • Provide day to day project support to the clinical safety department.
  • Support safety coordinators and managers with follow-up on cases.
  • Manage and maintain main mailbox and assist with triage.
  • Create and maintain project-related trackers and status reports.
  • Assist with case processing and reporting activities as delegated.
  • Conduct quality control reviews of departmental documents.
  • Perform other tasks as needed.

Qualifications

  • Administrative experience is beneficial.
  • Excellent organizational and prioritization skills are needed.
  • Knowledge of Microsoft Office required.
  • Knowledge of medical terminology, and an interest in clinical trials/drug development – desirable.
  • Applicants should have great attention to detail and excellent oral and written communication skills in English. Knowledge of Turkish language would be a plus.
  • University degree not required.

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.
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. #J-18808-Ljbffr

Project Assistant - Clinical Safety & Pharmacovigilance (office based in London) employer: Medpace, Inc.

Medpace is an exceptional employer that fosters a dynamic and supportive work culture in London, where employees are encouraged to grow their careers within the clinical safety and pharmacovigilance sector. With a flexible work environment, competitive compensation, and structured career paths, Medpace prioritises employee well-being and professional development, making it an ideal place for those looking to make a meaningful impact in the healthcare industry.
M

Contact Detail:

Medpace, Inc. Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Project Assistant - Clinical Safety & Pharmacovigilance (office based in London)

✨Tip Number 1

Familiarise yourself with clinical safety and pharmacovigilance concepts. Understanding the basics of drug development and safety protocols will help you engage in meaningful conversations during interviews.

✨Tip Number 2

Network with professionals in the clinical research field. Attend industry events or join online forums to connect with people who work at Medpace or similar organisations, as they can provide valuable insights and potentially refer you.

✨Tip Number 3

Demonstrate your organisational skills by preparing a project tracker or status report as a sample. This shows initiative and gives you a practical example to discuss during your interview.

✨Tip Number 4

Brush up on your Microsoft Office skills, especially Excel. Being proficient in creating and managing spreadsheets will be crucial for the role, and showcasing this ability can set you apart from other candidates.

We think you need these skills to ace Project Assistant - Clinical Safety & Pharmacovigilance (office based in London)

Organisational Skills
Prioritisation Skills
Attention to Detail
Excellent Oral Communication
Excellent Written Communication
Microsoft Office Proficiency
Knowledge of Medical Terminology
Project Tracking and Reporting
Quality Control Review
Case Processing Support
Email Management and Triage
Team Collaboration
Adaptability
Interest in Clinical Trials and Drug Development

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience, especially any administrative roles or skills that align with the responsibilities of a Project Assistant in Clinical Safety & Pharmacovigilance. Emphasise your organisational skills and attention to detail.

Craft a Compelling Cover Letter: Write a cover letter that showcases your enthusiasm for the role and the company. Mention your interest in clinical trials and drug development, and how your previous experiences make you a suitable candidate for this position.

Highlight Relevant Skills: In your application, specifically mention your proficiency in Microsoft Office and any knowledge of medical terminology. If you have experience with project management tools or trackers, be sure to include that as well.

Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. Clear and concise communication is key, so ensure your written English is polished and professional.

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

✨Showcase Your Organisational Skills

As a Project Assistant, you'll need to demonstrate excellent organisational and prioritisation skills. Be prepared to discuss specific examples from your past experiences where you successfully managed multiple tasks or projects simultaneously.

✨Familiarise Yourself with Medical Terminology

Having knowledge of medical terminology is desirable for this role. Brush up on relevant terms and concepts related to clinical trials and pharmacovigilance, as this will show your genuine interest and preparedness for the position.

✨Highlight Your Attention to Detail

Attention to detail is crucial in this role. Prepare to provide examples of how you've ensured accuracy in your previous work, whether through quality control reviews or meticulous case processing.

✨Demonstrate Communication Skills

Excellent oral and written communication skills are essential. Practice articulating your thoughts clearly and concisely, and be ready to discuss how you've effectively communicated with team members or stakeholders in past roles.

Project Assistant - Clinical Safety & Pharmacovigilance (office based in London)
Medpace, Inc.
Go Premium

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

M
  • Project Assistant - Clinical Safety & Pharmacovigilance (office based in London)

    London
    Full-Time
    28800 - 43200 £ / year (est.)

    Application deadline: 2027-08-11

  • M

    Medpace, Inc.

Similar positions in other companies
UK’s top job board for Gen Z
discover-jobs-cta
Discover now
>