senior analyst II

Project Farma (PF); Bengaluru; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Precision Medicine Group is seeking a Senior Analyst II to develop and maintain Tableau dashboards and SQL programs supporting clinical data management. You will analyze CRFs and protocol details to ensure accurate data handling across studies, while collaborating with clinical teams to drive data-driven decisions.

The role requires a strong technical background, knowledge of clinical trial domains, and a focus on data quality, discrepancy resolution, and documentation.

Qualifications

• Bachelor's degree or equivalent with healthcare/clinical domain preferred.
• 5+ years in a similar clinical/healthcare data role.
• Proficient in Tableau and Excel for visualization.
• Strong SQL knowledge for data management and queries.
• Good understanding of clinical trial domains and data management principles.
• Excellent analytical and problem-solving abilities.
• Strong verbal and written communication to collaborate with teams.
• High attention to detail and data accuracy.

Responsibilities

• Design, develop, and maintain Tableau dashboards for clinical data visualization.
• Create, manage, and optimize SQL databases and queries for trial data analysis.
• Analyze study requirements, CRFs, and protocol information for accurate data capture.
• Identify, investigate, and resolve data discrepancies to ensure data integrity.
• Collaborate with clinical teams to understand data needs and provide analytical support.
• Ensure data quality through validation and QC processes.

Skills

Tableau

Excel

SQL

Discrepancy management

Communication

Education

4-year college degree

Tools

Power BI

Python

R

Job description

Job Description

Position Summary

The Senior Analyst II will be responsible for developing and maintaining Tableau dashboards and SQL programming to support clinical data management and analysis. This role requires a strong technical background, a good understanding of various clinical trial domains, and expertise in data management, including discrepancy management. The successful candidate will analyze dashboard requirements based on Case Report Forms (CRFs) and protocol information to ensure accurate and efficient data handling for clinical studies. Essential functions of the job include but are not limited to:

Essential Functions of the job include but are not limited to

• Tableau Dashboard Development:Design, develop, and maintain interactive Tableau dashboards to visualize clinical trial data and support decision-making processes.
• SQL Programming:Create, manage, and optimize SQL databases and queries to store, retrieve, and analyze clinical trial data efficiently.
• Requirements Analysis:Analyze study requirements, Case Report Forms (CRFs), and protocol information to ensure accurate data capture and reporting.
• Discrepancy Management:Identify, investigate, and resolve data discrepancies to ensure data accuracy and integrity.
• Collaboration:Work collaboratively with clinical teams to understand their data needs and provide analytical support.
• Data Quality Assurance:Ensure the accuracy, integrity, and consistency of clinical trial data through rigorous data validation and quality control processes.
• Technical Documentation:Develop and maintain comprehensive technical documentation for all data management and analysis processes.
• Troubleshooting:Identify and resolve data-related issues promptly to ensure uninterrupted data flow and analysis.
• Continuous Improvement:Stay updated with the latest trends and best practices in data visualization, database management, and clinical data management.

Qualifications

Minimum Required:

• 4-year college degree or equivalent combination of education and experience, ideally in a business, scientific or healthcare discipline.
• 5-years proven experience in a similar role, preferably in a clinical or healthcare setting.
• Proficiency in Tableau and Excel for data visualization.
• Strong knowledge of SQL for database management and programming.
• Good understanding of various clinical trial domains and data management principles.
• Excellent analytical and problem-solving abilities.
• Strong verbal and written communication skills to effectively collaborate with clinical teams and stakeholders.
• High level of attention to detail and commitment to data accuracy

Other Required

• Established experience and fluency in the Microsoft Office package of programs (Outlook, Word, Excel, and PowerPoint)

Preferred

• Experience with other data visualization tools (e.g., Power BI).
• Knowledge of programming languages such as Python or R.
• Familiarity with clinical trial data and regulatory requirements.
• Certification in data management or related fields

Skills

• Demonstrates solid interpersonal skills.
• Demonstrates, or can be trained and retain a working knowledge of ICH-GCP, and relevant Precision SOPs and regulatory guidance.

Competencies

• Exhibits strong self-motivation, is detail-oriented and able to work and plan independently as well as in a team environment.
• Demonstrates professionalism, as evidenced by punctuality, ability to deliver on commitments, and maintain positive interactions with internal and external stakeholders.
• Communicates both verbally and in written form in an efficient and professional manner.
• Demonstrates values and a work ethic consistent with Precision Values and Company Principles.

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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [e-mail].