ACUTA
Providing Regulatory Information Management (RIM) solutions and services to the Life Sciences and related industry.
- Open roles
- 40
- New role every
- ~0.1 days
Company signals
Score: 69Job facts
- Location
- London, England, United Kingdom
- Type
- Full-time
- Posted
- Jun 02, 2026
More roles at ACUTA
- Asistente de Datos Junior · Bogota, Colombia
- Analyst (Consulting) · Mexico City, Mexico
- Clinical Research Coordinator, On-site, Elkhorn, NE · Elkhorn, NE, United States of America
- Site Research Assistant (Rosario) · Buenos Aires, Argentina
- Associate Director, HR · Durham, North Carolina, United States of America
- Regulatory and Start Up Specialist - Portugal · Lisbon, Portugal
Epidemiology Research Associate
at ACUTA
Job Overview
Assist in organizing and managing research projects including contribution to
development of study protocols, reports and data collection methods, arranging
and attendance at project meetings and traveling to client sites as needed.
May assist in preparation of abstracts, manuscripts and oral presentations
along with other related study documents.
Essential Functions
• Organizes and helps manage research projects.
• May serve as project manager for Scientific Affairs-based projects.
• Reviews data and study documents for content and quality control of medical
writing.
• Performs critical, systematic literature review and provides written
summaries as needed.
• Contributes to drafting of sections of study protocol and study reports with
the review and guidance of Project Lead.
• Assists in preparation of abstracts, manuscripts and oral presentations,
including development of slides and posters for presentation of project
results at conferences.
• Provides consistency in overall project team support and act as a resource
for internal team members.
• May participate in client-facing project meetings as a recognized member of
the project team and directly interface with client project team in order to
coordinate deliverables.
• May conduct statistical analysis as needed.
Qualifications
• Bachelor's Degree with 1 year relevant education and experience Req
• Master's Degree Public health, epidemiology, outcomes research, health
economics or a relevant scientific field Pref
• Sound methodological training in epidemiology, outcomes research, health
economics, or related area relevant to observational health research.
• Strong oral and written communication skills, medical writing experience
beneficial.
• Ability to establish and maintain effective working relationships with
coworkers, managers and clients in a global and matrixed environment.
• Exceptional attention to detail and the ability to effectively prioritize
and manage multiple tasks.
• Ability to work independently, both under supervision and as a contributing
team member.
• Must be proficient in Word, Excel, PowerPoint and Internet Explorer;
knowledge of SAS preferred.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.