Clinical Research Specialist - Remote

Overview

The Clinical Research Specialist plays a crucial role in ensuring that clinical trials are conducted according to regulatory requirements, driving evidence needed to optimize patient outcomes in the field of cardiovascular therapies.

In Short

• Conduct and report clinical trials in compliance with regulatory standards.
• Perform study start-up and management activities.
• Identify and address discrepancies in study documentation.
• Participate in audits to ensure compliance with documentation practices.
• Collaborate with cross-functional teams for data management.
• Manage study progress and communicate with stakeholders.
• Propose solutions to improve process efficiency.
• Travel up to 25% as required.
• Maintain confidentiality and manage competing priorities.
• Work in a team environment to achieve clinical objectives.

Requirements

• Bachelor's Degree in Life Sciences or Nursing.
• 3 years of experience in clinical research or related fields.
• Experience with regulatory compliance and quality assurance.
• Knowledge of cardiovascular physiology preferred.
• Clinical research certification is a plus.
• Proficient in MS Office and clinical systems.
• Strong communication and analytical skills.
• Attention to detail and problem-solving abilities.
• Ability to work under pressure in a fast-paced environment.
• COVID-19 vaccination required for patient-facing roles.

Benefits

• Competitive salary based on experience.
• Performance-based incentives.
• Diverse benefits programs for employees and families.
• Opportunities for professional development.
• Supportive team environment.
• Commitment to employee well-being.
• Global leader in patient-focused medical innovations.
• Focus on improving patient outcomes.
• Collaboration with leading clinicians and researchers.
• Innovative work culture.