Responsibilities

• Oversee data management activities for one or more clinical projects, ensuring adherence to project protocols.
• Serve as the primary point of contact for clients and project leads regarding all data management activities.
• Guide team members in applying relevant components of the project protocol to their daily tasks.
• Collaborate with senior team members to manage individual studies, especially those with limited volume or complexity.
• Maintain clear communication with management about all data management activities within the studies.
• Develop and implement data management plans and timelines to ensure project milestones are met.
• Analyze and validate data to ensure accuracy and integrity.
• Provide training and support to team members and stakeholders on data management processes.

Requirements

• Bachelor’s degree in a relevant field; advanced degree preferred.
• Proven experience in clinical data management, ideally within the pharmaceutical or biotech industries.
• Strong understanding of clinical trial processes and regulatory requirements.
• Excellent leadership and team management skills.
• Effective communication skills, both verbal and written.
• Ability to work independently and collaboratively in a fast-paced environment.
• Strong analytical and problem-solving abilities.

Benefits

• Competitive salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance.
• Generous paid time off and holiday policies.
• Opportunities for professional development and career advancement.
• A supportive and inclusive work environment.
• The chance to work on groundbreaking projects that significantly impact the pharmaceutical industry.