Senior Clinical Data Coordinator – Catalyst Clinical Research (Remote)
Job Summary:
Catalyst Clinical Research is hiring a Senior Clinical Data Coordinator (Sr. CDC) to lead data management activities in support of global clinical trials. This fully remote opportunity is ideal for experienced data professionals skilled in EDC, SAS, and clinical trial standards who want to drive high-impact projects across oncology and multi-therapeutic studies. The Sr. CDC will ensure the integrity, consistency, and timely availability of clinical data for regulatory submissions and publications.
Key Responsibilities:
Perform and document user acceptance testing (UAT) of eCRF builds and edit checks
Develop, validate, and manage clinical data per protocol and regulatory standards
Create and peer-review data management documentation and processes
Support SAE reconciliation and ensure consistency with safety databases
Collaborate with coding specialists to maintain quarterly coding reviews
Review manual data listings, raise and resolve queries, and assist with query management
Coordinate data transfers and perform vendor data reconciliation (e.g., PK/PD, labs, imaging)
Review blind data and assist with blind data review meetings
Perform final patient data review and database lock
Support and mentor Clinical Data Coordinators; provide peer review on CRF design
Participate in cross-functional team meetings; document meeting minutes
Serve as backup to Lead Data Manager (LDM) as needed
Required Skills & Qualifications:
Bachelor's degree in a life science or related discipline with 3+ years of clinical data experience
(or high school diploma with 4+ years of relevant experience)
Expertise in EDC systems and SAS for clinical data processing
Strong knowledge of ICH-GCP and data quality standards in clinical trials
Proficient in Microsoft Office Suite
Exceptional written, verbal, and presentation communication skills
Highly organized with strong analytical and time-management abilities
Proven ability to manage multiple clinical projects and shifting priorities
Strong judgment, problem-solving, and interpersonal skills
Experience in oncology trials or global CRO settings is a plus
Perks & Benefits:
Remote work flexibility with global collaboration
Opportunity to work on cutting-edge oncology and multi-therapeutic trials
Collaborative and inclusive work culture
Competitive compensation based on experience
Career advancement opportunities in a growing CRO
Access to training, mentoring, and continuous learning initiatives
Company Overview:
Catalyst Clinical Research is a global contract research organization (CRO) offering flexible, scalable solutions to the biopharma industry. Through Catalyst Oncology and Catalyst Flex, the company supports a wide range of therapeutic areas, empowering clinical development with innovation, global expertise, and operational excellence.
Work Mode: Remote
Job Type: Full-time
Ready to Shape the Future of Clinical Data?
If you are passionate about ensuring data accuracy in global clinical trials and are ready to grow with a dynamic CRO, apply now and join Catalyst Clinical Research in advancing life-saving therapies.
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