Senior Clinical Research Associate - Romania - Remote

## About the Role As a Senior Clinical Research Associate at Worldwide, you will be responsible for managing research activities at sites participating in clinical research projects. This will involve identifying potential sites, performing study start-up activities, and training sites to collect data properly. You will work closely with a team of experts across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. The role requires a strong understanding of clinical research principles, as well as excellent interpersonal and organizational skills.

The Clinical Operations team at Worldwide is committed to advancing clinical research and improving patient outcomes. As a Senior Clinical Research Associate, you will play a critical role in this mission, working alongside brilliant minds to drive study success. You will have the opportunity to work on a wide range of projects, from registries to non-interventional studies, and will be supported by a team of experienced professionals.

Worldwide is a global, mid-size CRO that prides itself on its innovative approach to clinical research. The company is committed to enabling professionals from all backgrounds and experiences to succeed, and prioritizes cultivating a diverse and inclusive environment.

## What You Will Do - Manage research activities at sites participating in clinical research projects - Identify potential sites and perform study start-up activities - Train sites to collect data properly and report potential safety-related events - Conduct study initiation visits (SIVs) - Ensure compliance with regulatory requirements and obtain informed consent - Manage site activities during study maintenance and close-out - Collaborate with cross-functional teams, including data management and biostatistics - Develop and implement study protocols and amendments - Manage and maintain accurate and complete study records - Participate in internal audits and quality assurance activities

## What We Are Looking For - 2+ years of experience as a Clinical Research Associate - 4-year university degree or RN/BSN in Nursing - Experience in Hematology, Oncology, and Cardiometabolic (Obesity, T1D/T2D, GLP) - Excellent interpersonal, oral, and written communication skills in English - Superior organizational skills with attention to detail - Proficiency in Microsoft Office, CTMS, and EDC Systems - Ability to work with little or no supervision - Willingness to travel (up to 25%)

## Nice to Have - Experience with electronic data capture (EDC) systems - Knowledge of ICH-GCP and regulatory requirements - Certification in clinical research (e.g., CCRA, CCRP) - Experience in project management and team leadership

## Benefits and Perks - Competitive salary and benefits package - Opportunity to work on diverse and challenging projects - Collaborative and dynamic work environment - Professional development and training opportunities - Flexible work arrangements, including remote work options - Access to cutting-edge technology and tools - Recognition and reward for outstanding performance

- Tip: Make sure your resume is tailored to the job description, highlighting your experience in clinical research and relevant skills.

• Tip: Prepare to talk about your experience with Excel and other tools, and be ready to provide specific examples of how you've used them in previous roles.
• Tip: Research the company and the therapeutic areas they work in, and be prepared to discuss your knowledge and interest in these areas.
• Tip: Be prepared to discuss your experience working independently and managing multiple projects simultaneously.
• Tip: Consider obtaining certification in clinical research (e.g., CCRA, CCRP) to demonstrate your expertise and commitment to the field.