Senior Analyst - Clinical Data Management

Join Stryker: Leading the Future of Stroke Care as a Staff Biostatistician

Work Flexibility: Hybrid or Onsite

About Stryker

Stryker is a global leader in medical technology, dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. Our diverse array of innovative medical technologies—including reconstructive, medical and surgical, neurotechnology, and spine products—enable people to lead more active and satisfying lives. We are currently seeking a Staff Biostatistician to join our Neurovascular division in Gurgaon, Haryana.

About the Neurovascular Division

Stryker’s Neurovascular division is focused on advancing less invasive stroke therapies through its Complete Stroke Care solutions. Our innovative stroke products and services for ischemic and hemorrhagic stroke are complemented by our commitment to providing clinical education and support to help physicians deliver better patient outcomes. Our product portfolio includes stent retrievers, detachable coils, stents, balloons, guidewires, and microcatheters. We are proud to be named one of the FORTUNE 100 Best Companies to Work For, ranking 11th in 2016.

If you join our organization, you will be working to “Make Stroke History.” Stroke is a devastating condition responsible for 1 in 20 deaths, according to the CDC. Watch how Stryker is making a difference:

Who We Want

• Detail-oriented process improvers: Critical thinkers who naturally see opportunities to develop and optimize work processes—finding ways to simplify, standardize, and automate.
• Strategic thinkers: Individuals who enjoy analyzing data or trends for planning, forecasting, advising, budgeting, reporting, or sales opportunities.
• Collaborative partners: People who build and leverage cross-functional relationships to bring together ideas, data, and insights to drive continuous improvement.
• Analytical problem solvers: Experts who go beyond just fixing issues by identifying root causes, evaluating optimal solutions, and recommending comprehensive upgrades.
• Dedicated achievers: Individuals who thrive in a fast-paced environment and will stop at nothing to ensure a project meets regulations and expectations.

Qualifications and Experience

• 6 to 12 years of relevant experience
• Preferred: Experience in Medical Devices
• Preferred: Pharmacy, Nursing, or Medical Graduation/Post-graduation
• Preferred: Any Graduation with Clinical Research post-graduation
• Preferred: Knowledge of clinical trial design and analysis
• Preferred: Knowledge of regulatory guidelines (FDA/CFR; ISO14155)
• Preferred: Experience supporting publication of analysis results (e.g., abstracts, posters, manuscripts)
• Preferred: Experience with electronic data capture (EDC) systems
• Excellent oral and written communication skills
• Ability to explain basic statistical concepts to non-statisticians
• Good organizational and time management skills

What You Will Do

Data Review and Data Medical Review

• Identify data discrepancies such as missing data, potentially discrepant, and mismatching data with other fields
• Identify potential data discrepancies from medical and clinical perspectives
• Collaborate with Medical Sciences for medical and product coding review and approval

Data Querying and Integrity Management

• Lead the data querying and completion process during data review
• Generate data discrepancy criteria and associated queries during data review
• Develop and publish data entry metrics periodically
• Analyze data fields to detect suspicious data activities

Data Cleaning

• Address non-standard data identified during the review process
• Coordinate with CRAs for data completion and correction
• Develop complex status reports to determine follow-up actions

Base Data Management Process

• Coordinate Case Report Form (CRF)