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Medspace

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

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

Posted 5 days ago

StirlingOn-Site

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

Medspace

Permanent
Full-Time
Sign up to unlock the estimation.Sign up to unlock the estimation~£22,000 - £28,000per annum· Meev estimate

Posted 5 days ago

Description

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 Stirling. 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.
  • National 5 (English, Science, Maths A - C), Highers or Advanced Highers – desirable. 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 6,000 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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Medspace

A scientifically driven global CRO accelerating clinical development for biotech and pharma.

CincinnatiContract Research1000+
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Medspace

Contract Research

Shape the future of medicine by embedding deep scientific expertise into the most innovative clinical trials. Work alongside cross functional experts who turn complexity into clarity, trusted by biotech to accelerate treatments that matter.

Click to learn more
Medspace logo

Medspace

Contract Research

Shape the future of medicine by embedding deep scientific expertise into the most innovative clinical trials. Work alongside cross functional experts who turn complexity into clarity, trusted by biotech to accelerate treatments that matter.

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