PHARMAFull-time
Clin Data Assoc II/Senior Clin Data Assoc
By Admin · Clinical Data Management
REMOTE (IN)REMOTEPOSTED: 9/12/2026
PHARMAFull-time
HIRING ORGANIZATIONTHERMO FISHER SCIENTIFICLife Sciences / Scientific Instruments / Biotechnology
ROLE OVERVIEW
Clinical Data Associate II/Senior Clinical Data Associate role supporting high-quality, analysis-ready clinical trial data through advanced data review, cleaning, reconciliation, query management, and inspection readiness.
ROLE DEFINITION & RESPONSIBILITIES
- •Identify, resolve, and update clinical data discrepancies
- •Generate, track, and resolve data clarifications and queries
- •Implement CRF design in identified graphic design packages when required
- •Review data listings for accuracy and consistency
- •Analyze and resolve data validation and other data management reports
- •Produce project-specific status reports for CDM management and clients
- •Perform SAE and third-party vendor reconciliations
- •Support end-to-end clinical study delivery, data quality, risk management, and inspection readiness
Reporting Hierarchy: Works within the PPD Clinical Research/FSP Data Management team and collaborates with global client data science teams, CDM management, clients, CROs, vendors, and country operations.
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's degree or equivalent relevant formal academic qualification
- 4+ years of experience in Clinical Data Management
- Experience with RAVE or Veeva EDC
- Knowledge of clinical trial terminology and study protocols
- Understanding of Data Validation Manuals
- Strong English communication, organization, analytical, and problem-solving skills
PREFERRED QUALIFICATIONS
- •Experience in global clinical studies across phases and therapeutic areas
- •Experience working within an FSP/CRO environment
- •Exposure to AI-enabled clinical trial technologies
- •Experience with project management, financial tracking, risk management, or data standards/programming
REQUIRED VERIFIED SKILLS
Clinical Data Management
RAVE
Veeva EDC
clinical trial data review
data cleaning
data reconciliation
SAE reconciliation
third-party vendor reconciliation
data validation
CRF design
GCP
SOPs
Data Validation Manual
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Global exposure, continuous learning, tailored learning pathways, stretch assignments, mentorship, end-to-end study ownership, and exposure to modern clinical data management and AI-enabled workflows.
No salary, bonus, or equity information is explicitly disclosed in the provided posting.
ORGANIZATION CONTEXT & CULTURE
Thermo Fisher Scientific is a global science and healthcare company providing technologies, services, and solutions for life sciences research, diagnostics, clinical development, and pharmaceutical manufacturing.
TEAM SIZE: 90,000+ employees
INDUSTRY: Life Sciences / Scientific Instruments / Biotechnology
Culture: Science-driven, collaborative, quality-focused environment with emphasis on customer impact, continuous learning, global teamwork, and innovation.
EXPECTED CAREER ROADMAP
Potential progression through the Clinical Data Management track into Senior CDM, Clinical Data Team Lead, or CDM Project Manager roles, with alternative pathways into Data Standards or Programming based on skills and business needs.
APPLICATION ADVISORY
Emphasize 4+ years of clinical data management experience and hands-on RAVE/Veeva EDC expertise; highlight SAE and vendor reconciliation, data cleaning, query management, validation reporting, GCP/SOP compliance, and global study experience; demonstrate strong analytical and stakeholder communication skills.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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