Clinical Data Analyst III

About This Opportunity

We are representing a confidential clinical research organization seeking an experienced Clinical Data Analyst III to join their team in India. Our client is looking for a seasoned professional who can independently lead clinical data validation and data management activities while serving as a subject matter expert and mentor to junior team members.

Responsibilities

• Independently perform and lead clinical data validation, cleaning, review, and reconciliation activities throughout study conduct and database lock
• Manage data queries and conduct manual and SAS-generated listing reviews
• Perform reconciliation of external vendor data and ensure data integrity across systems
• Identify project risks, highlight delivery concerns, and support mitigation planning
• Lead User Acceptance Testing (UAT) activities for clinical database setups
• Review study protocols, EDC screens, and database configurations
• Provide input into data management timelines and coordinate operational activities during study start-up
• Perform quality control reviews and ensure compliance with SOPs, ICH-GCP guidelines, and regulatory requirements
• Act as a mentor and provide on-the-job training to Clinical Data Analysts
• Serve as a Subject Matter Expert for data management tools, systems, and processes
• Support continuous improvement initiatives and implementation of project-specific tools and efficiencies
• Act as backup to the Data Management Lead when required

What We're Looking For

Education & Experience:

• Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or a related healthcare discipline
• Relevant experience in Clinical Data Management within the clinical research or CRO industry

Technical Requirements:

• Strong experience with Clinical Data Management Systems such as Medidata Rave, Oracle InForm, Veeva, DataLabs, or ClinBase
• Advanced understanding of clinical data management processes, including data cleaning, reconciliation, and database lock activities
• Expertise in database setup activities and data validation specifications
• Knowledge of MedDRA and WHODrug coding dictionaries
• Understanding of CDISC standards
• Basic knowledge of SAS and programmed listings
• Strong knowledge of ICH-GCP guidelines, clinical research regulations, and industry best practices
• Experience leading virtual data management teams across global studies

Professional Skills:

• Strong leadership and collaboration skills with the ability to coordinate global and virtual teams
• Ability to independently interact with sponsors and stakeholders regarding data issues and study requirements
• Strong negotiation, influencing, and stakeholder management skills
• Advanced problem-solving and root cause analysis capabilities
• Exceptional attention to detail and commitment to first-time quality
• Strong organizational, prioritization, and time-management skills
• Excellent written and verbal communication skills
• Effective presentation and knowledge-sharing abilities
• Strong mentoring and coaching skills

How We Work With You

When you apply through Get A Job.ai, our experienced recruiting team will review your qualifications and conduct an initial screening. If there's a strong match, we will submit your profile to our client for consideration. Please note that all applications must go through Get A Job.ai—do not contact the client directly.

Pay

Compensation details will be discussed during the screening process based on experience and qualifications.

Equal Employment Opportunity: Get A Job.ai is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.