Clinical Data Manager, External Site Studies
💰 $80,000 – $130,000/yr
Job Description
About This Opportunity
Celerion is seeking a skilled Clinical Data Manager for External Site Studies to join our remote team. This is a full-time position dedicated to ensuring the highest standards of data integrity and regulatory compliance across external site clinical trials. If you're passionate about accelerating life-saving treatments to market and thrive in a fast-paced research environment, this role offers a meaningful opportunity to make a direct impact.
About Celerion
Celerion is committed to enabling swift, exceptional clinical research through translational medicine. Every day, our experienced team leverages agility and innovative research strategies to help get critical drugs to market faster. We support a business dedicated to creating treatments that save lives, and our employees are at the heart of that mission.
The Role: Clinical Data Manager, External Site Studies
As a Clinical Data Manager, you will provide expert oversight of end-to-end data management for external site clinical trials. Your responsibilities will include:
- Data Integrity & Compliance: Ensure data integrity, regulatory compliance, and timely delivery of high-quality datasets across all assigned studies
- EDC System Management: Leverage both Celerion-provided and Sponsor-provided Electronic Data Capture (EDC) systems to maintain accurate and complete clinical datasets
- Database & Software Proficiency: Utilize various database systems and specialized software tools to efficiently manage, organize, and clean clinical data throughout the entire study lifecycle
- Cross-Functional Collaboration: Work seamlessly with internal teams and external partners to coordinate data management activities and resolve issues
- Sponsor Communication: Maintain direct communication with Sponsors to provide updates, address inquiries, and ensure alignment on project objectives
- Project Timeline Management: Actively manage and track project timelines to ensure all deliverables meet agreed-upon deadlines
- Quality Assurance: Conduct thorough data validation, quality checks, and cleaning procedures to maintain regulatory and study protocol compliance
- Issue Escalation: Identify, document, and appropriately escalate data-related issues and discrepancies
Ideal Candidate Profile
This role is perfect for a proactive data management professional who possesses:
- Strong ownership mentality for assigned studies and deliverables
- Sound judgment in making day-to-day operational decisions
- Excellent prioritization skills when managing multiple concurrent projects
- Ability to communicate effectively with both internal teams and external stakeholders
- Demonstrated capacity to escalate issues appropriately and facilitate timely resolution
- Detail-oriented approach to ensuring data accuracy and completeness
- Familiarity with clinical trial operations and regulatory requirements
- Experience with EDC systems and database management tools
Why Join Celerion?
This is a fully remote position, offering flexibility while being part of a mission-driven organization. You'll work on meaningful projects that directly contribute to bringing innovative treatments to patients. The role provides opportunities to develop expertise in clinical data management, work with diverse therapeutic areas, and collaborate with industry-leading Sponsors and research teams.
Key Work Environment Details
Location: 100% Remote - United States
Employment Type: Full-Time
Travel: Minimal to none (fully remote)
💰 Compensation not publicly listed. Market estimate for similar roles: from $80K, varying by experience and location.