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Sr Clinical Data Coordinator

3+ years
Not Disclosed
10 July 29, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

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.