Senior Clinical Data Scientist

Department Icon Data Science Analytics & Machine Learning
149+ Applicants
Posted: 1 hour ago
5-10 years
Hyderabad (Office), India
work from office

Posted: 1 hour ago
|
Applicants: 149+
Job Description
About Company
Similar Jobs
Please verify your account first! Send OTP

Job Description

Summary

-Provide timely & professional ongoing Mgmt of Data Mgmt/Coding/CDDRA-Database Development/DAP deliverables and of clinical trial data with respect to cost, quality and timelines for all assigned trials within Clinical Data Mgmt. Ensure consistently high quality data available for analysis and reporting. Develop content and redefine training modules into engaging & interactive applications. Leverage technology to ensure process simplification and training delivery. Follows Good Clinical Practices (GCP), data-handling procedures and guidelines. Participates in the review of clinical research protocols, reports and statistical analysis plans. Drives participation and input within Data Operations (DO) in the delivery of quality data and programs, processes and documentation -Manage data Load, Transfer and conform of Clinical trial data to NCDS compliant standards. The position is a key contributor with Data Provisioning team in ensuring that pharmaceutical drug-development plans in Novartis Global Drug Development are executed efficiently with timely and high quality deliverables.


 

Major accountabilities:

  • Provides DM leadership across assigned trial (s) and Acts as the Trial Data Manager where needed -Demonstrates a business understanding of the compound (s) profile to identify and assist in successful application of data Mgmt processes.
  • Provides feedback to assure well written protocols and amendments.
  • Recognize and resolve protocol issues that may impact database design, data validation and /or analysis/reporting and that do not make the best use of available standards -Performs DM activities for start up of a study, Data Handling plan , Data Review Plan and performing user acceptance testing (UAT) -Manage local lab set up for the Clinical Database as applicable -Leads process and training deliverables within platform or processes.
  • Accountable for all aspects of the Process and Training within remit to ensure full compliance to all applicable global regulatory requirements is maintained and business objectives are achieved.
  • Accountable for all quality related aspects -Centralizes and aligns DO for audits and inspections.
  • Manages and measures Quality -Coordinates exception requests, deviations and corrective /preventative action plans -Performs DM hands on activities during the course of the study Performs ongoing review of all data generated from the clinical study including Third party and local lab data as well as SAE reconciliation where applicable -Responsible and accountable to ensure consistency of assigned trials with program level standards across DM documentation -Has proven abiity to use the tools available to generate listings for data review and where necessary provides these to the study teams.
  • Generates the study status reports for use at Clinical trial team meetings.
  • Supports and assists Junior staff for assigned trials -Provides effective input into DM initiatives and innovations for quality, efficiency and continuous improvement in scientific and operational excellence -Leads /Coordinates synonym review activities and dictionary version upgrade activities at trial /Program level.
  • Serves as primary study lead ensuring timely and quality deliverables by establishing and maintaining strong working relationships with study teams, and functional lines.
  • Acts as a technical consultant as required.

Minimum Requirements

    Looking to get Placed? Try our Placement Guarantee Plan

  • Ability to work under pressure demonstrating agility through effective and innovative team leadership
  • Excellent interpersonal skills and proven ability to operate effectively in a global environment. Ability to influence and communicate across functions and to external stakeholder
  • Proven ability to interrogate and view data though various programming/GUI techniques
  • Excellent problem-solving skills
  • Ideally 4 years’ experience in Drug Development with at least 3 years in Clinical Data Management
  • Excellent verbal and written skills


 

Skills Desired

Clinical Data Management, Data Governance, Data Integrity, Data Management, Data Quality, Data Science, Waterfall Model

Skills

Data ScienceGCPReconciliationComplianceLeadershipTeamsClinical ResearchClinical Data Management

If a job posting appears fraudulent, asks for payment, contains misleading information, or violates our guidelines, please report it immediately. Our team will review it promptly, Jobaaj does not charge any fee from the applicants.

About Company

Novartis is a global healthcare giant, renowned for its focus on innovative pharmaceuticals and healthcare solutions. Based in Switzerland, the company operates in over 140 countries, striving to address some of the most challenging health issues. Novartis careers offer a plethora of opportunities across research, pharmaceutical development, digital health, and patient support, making it an ideal workplace for those passionate about making a significant impact in healthcare. Employees at Novartis are part of a culture that values high ethical standards, diversity, and professional development, all while working towards reimagining medicine to improve and extend people’s lives.


Read More

Important dates & deadlines?

Application Deadline

25 Nov 26, 12:25 AM IST

Similar Jobs

View All
Loading...
Bag Logo
Jobaaj
Don't Miss out any Updates

Subscribe now for the latest job alerts
and never miss an update

Job Alert
Google hiring for Specific Roles Apply Now!
1 min ago
New Opportunity
Amazon is hiring freshers Apply Now!
5 min ago
Featured Jobs
Microsoft opening 50+ positions Apply Now!
10 min ago

Senior Clinical Data Scientist

Share with