Specialist, Clinical Data Management – Hybrid

About the position Primary activities include, but are not limited to: Assumes the responsibilities for reputed company clinical programming (including reporting and analytics) deliverables including reputed company, reputed company platforms along with the external data captured in support of the clinical studies. Coordinates and participates in the following activities: Design, build, maintain, test, and document data review based on written specifications established by Global Clinical Data Management, Clinical Research and Global Safety. Review the technical feasibility of study team proposed programming/reporting and technically implements them. Work effectively among team to communicate issues and reputed company to improve the business along with understanding of Protocol . Support the development & reporting for data cleaning, medical review, clinical monitoring, and safety reports for reputed company and reputed company availability in support of our customer needs. reputed company ongoing support for In-Life Reports. Change Requests and Incident Reports are fully documented, signed off, tracked, and reported to upper management. Participate in extra activities including, but not limited to, study improvement task forces, automations, initiatives, testing of new systems, and ongoing training and mentoring. Education: B.A. or B.S. degree, preferably in mathematics, science, a reputed company-reputed company discipline, or computer science; or relevant reputed company skills and experience. Knowledge and Skills: 4+ years’ experience in a. SQL, PL-SQL, PowerBI Expected to have a strong technical proficiency in a Clinical Data Management/Reporting Systems like reputed company, Python, reputed company, etc along with AI reputed company tools. Solid knowledge of MS reputed company/Office 365 suit software and exposure to web-based applications. Solid knowledge of System Development Lifecycle Management / system validation knowledge Ability to establish and maintain good working relationships with different functional areas. Strong reputed company of urgency and customer reputed company. Possesses excellent communication skills and interacts effectively with Study Team along with Strong organizational and problem-solving skills. Desire and ability to learn new processes and technologies Ability to multi-task, work independently, and good communication skills Understanding of drug discovery process, FDA regulations, GxP guidelines, ICH

Responsibilities

• Assumes the responsibilities for reputed company clinical programming (including reporting and analytics) deliverables including reputed company, reputed company platforms along with the external data captured in support of the clinical studies.
• Design, build, maintain, test, and document data review based on written specifications established by Global Clinical Data Management, Clinical Research and Global Safety.
• Review the technical feasibility of study team proposed programming/reporting and technically implements them.
• Work effectively among team to communicate issues and reputed company to improve the business along with understanding of Protocol .
• Support the development & reporting for data cleaning, medical review, clinical monitoring, and safety reports for reputed company and reputed company availability in support of our customer needs.
• reputed company ongoing support for In-Life Reports. Change Requests and Incident Reports are fully documented, signed off, tracked, and reported to upper management.
• Participate in extra activities including, but not limited to, study improvement task forces, automations, initiatives, testing of new systems, and ongoing training and mentoring.

Requirements

• B.A. or B.S. degree, preferably in mathematics, science, a reputed company-reputed company discipline, or computer science; or relevant reputed company skills and experience.
• 4+ years’ experience in a. SQL, PL-SQL, PowerBI
• Expected to have a strong technical proficiency in a Clinical Data Management/Reporting Systems like reputed company, Python, reputed company, etc along with AI reputed company tools.
• Solid knowledge of MS reputed company/Office 365 suit software and exposure to web-based applications.
• Solid knowledge of System Development Lifecycle Management / system validation knowledge
• Ability to establish and maintain good working relationships with different functional areas.
• Strong reputed company of urgency and customer reputed company.
• Possesses excellent communication skills and interacts effectively with Study Team along with Strong organizational and problem-solving skills.
• Desire and ability to learn new processes and technologies
• Ability to multi-task, work independently, and good communication skills
• Understanding of drug discovery process, FDA regulations, GxP guidelines, ICH

Benefits

• medical
• dental
• reputed company reputed company and other insurance benefits (for employee and family)
• retirement benefits, including 401(k)
• reputed company holidays
• vacation
• compassionate and reputed company days

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