Clinical Research Job at IQVIA, Europe
Are you looking for a career as a Clinical Research Associate? This Clinical Research Job at IQVIA Careers in Europe offers an opportunity to work on clinical trials, ensuring studies are conducted in accordance with regulatory guidelines and protocols. Join a global healthcare company and contribute to advancing medical research and patient outcomes.
About the Company:
IQVIA is a leading global provider of clinical research services, healthcare intelligence, and commercial insights. The company supports life sciences organizations in accelerating the development and commercialization of innovative treatments to improve patient health worldwide.
Job Details:
- Job Title: Clinical Research Associate
- Location: Sofia, Bulgaria
- Job Type: Full Time
- Work Mode: Field-Based
- Job ID: R1536756
- Industry: Clinical Research / Healthcare
Key Responsibilities:
- Perform site monitoring visits, including initiation, monitoring, and close-out in this Clinical Research Job at IQVIA Careers
- Ensure compliance with Good Clinical Practice (GCP) and ICH guidelines
- Support subject recruitment planning and tracking
- Conduct site training and maintain communication with study sites
- Evaluate the quality and integrity of clinical trial processes in this Clinical Research Job
- Track study progress, including submissions, enrollment, and data management
- Maintain Trial Master File (TMF) and Investigator Site File (ISF) at IQVIA Careers
- Prepare monitoring reports and follow-up documentation
- Collaborate with study teams for project execution in this Clinical Research Associate Role.
- Manage site financials and clinical trial agreements where applicable
Educational Requirements for this Job:
- Bachelor’s degree in a scientific or healthcare discipline preferred
- An equivalent combination of education, training, and experience may be considered
Skills Required:
- Minimum 1 year of on-site monitoring experience
- Knowledge of Good Clinical Practice (GCP) and ICH guidelines
- Strong understanding of clinical trial protocols
- Proficiency in Microsoft Word, Excel, and PowerPoint
- Good communication skills in English (written and verbal)
- Organizational and problem-solving abilities
- Time and financial management skills
- Ability to build effective professional relationships
Benefits of the Clinical Research Job:
- Opportunity to work with a global leader in clinical research
- Exposure to international clinical trials and regulatory processes
- Career growth in the healthcare and life sciences industry
- Hands-on experience in site monitoring and study management
- Contribution to improving global patient health outcomes
