Sr Clinical Data Scientist

Syneos Health

0-2 years

Not Disclosed

Remote

10 Oct. 4, 2025

Job Description

Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

🧑‍💻 Position Title:

Sr Clinical Data Scientist

🌍 Location:

IND-Remote

🆔 Job ID:

25102064

⏰ Shift:

4:30 PM – 1:30 AM IST

🎯 Job Overview:

Responsible for the end-to-end coordination of cross-functional clinical data collection and cleaning activities, ensuring study data deliverables are fit for purpose and meet sponsor expectations and contractual timelines. Serves as Functional Lead for Clinical Data Science and central steward of clinical data quality.

🌟 Key Responsibilities:

🔹 Functional Leadership & Project Oversight

Serve as primary contact for internal liaison between Clinical Data Science, Project Management, Clinical Monitoring, and other functional groups.
Lead and coordinate the Clinical Data Science team on assigned projects.
Mentor and train new or junior team members.
Review and maintain project plans, specifications, and documentation in line with SOPs.
Participate in internal, sponsor, and third-party meetings, audits, and proposal/bid defense meetings.

🔹 Clinical Data Science & Quality

Act as central steward of clinical data quality, monitoring risks using high-level protocol knowledge.
Identify required data elements and data quality oversight steps to support project analysis.
Coordinate cross-functional data cleaning activities to meet quality standards and timelines.
Develop clinical data acquisition plans and data flow diagrams aligned with protocol and regulatory requirements.
Perform analytic reviews, detect unreliable data, and recommend corrective actions.
Maintain compliance with ALCOA++ principles, ICH/GCP guidelines, and SOPs.

🔹 Communication & Reporting

Communicate, address, and resolve data-related questions with cross-functional teams.
Escalate issues impacting patient safety or study analysis.
Monitor project progress and report to sponsors using project status reports and tracking tools.
Maintain Trial Master File (TMF) and other documentation to support internal/external audits.

🔹 Resource & Budget Management

Plan, manage, and request Clinical Data Science resources.
Track budgets and identify out-of-scope activities for necessary change orders.

🎓 Qualifications & Requirements:

Education: BA/BS in Biological Sciences, Computer Sciences, Mathematics, Data Sciences, or related fields; MS preferred.
Clinical Data Science experience or equivalent combination of education and experience.
Proficiency with relational database management and Clinical Data Science systems.
Knowledge of drug development, risk-based approaches, biometrics, and workflow processes.
Strong project management, analytical, and staff leadership skills.
Experience with analytic modeling methods (regression, classification, clustering) preferred.
Proficiency in data analysis/visualization tools: Python, R, Spotfire, SAS.
Strong knowledge of medical terminology, clinical data, and regulatory requirements (ICH/GCP).
Effective oral/written communication and presentation skills.
Ability to multitask, prioritize, and work independently or as part of a multi-disciplinary team.

⚡ Work Environment & Physical Requirements:

Office/remote-based, occasional travel up to 25%.
Stationary for 6–8 hours/day.
Repetitive hand movements, occasional crouching, bending, twisting.
Light to moderate lifting (15–20 lbs).
Regular and consistent attendance; ability to work varied hours.

🌐 Why Syneos Health:

Work across 110 countries with global impact on clinical development.
Engage in a collaborative, innovative, and inclusive culture.
Opportunities for professional growth, career development, and recognition.

⚖️ Additional Information:

Tasks and responsibilities are not exhaustive; company may assign additional duties.
Equivalent experience, skills, and/or education may be considered.
Compliant with Americans with Disabilities Act (ADA); reasonable accommodations provided when appropriate.

📌 Summary:

Responsible for cross-functional data coordination, cleaning, and quality oversight to ensure clinical study deliverables are accurate, compliant, and aligned with sponsor expectations.

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Sr Clinical Data Scientist

Job Description

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