Senior Data Scientist Role
We are seeking a Senior Data Scientist to join our team. As a key contributor, you will be responsible for managing data management and ensuring timely delivery of clinical trial data. Your primary focus will be on providing high-quality data for analysis and reporting, while also developing and implementing processes to improve efficiency and quality.
* Key Responsibilities:
* Data Management Leadership: Provide leadership across assigned trials, acting as the Trial Data Manager where needed.
* Data Provisioning: Ensure that pharmaceutical drug-development plans are executed efficiently with timely and high-quality deliverables.
* Process Improvement: Identify and implement process improvements to enhance data management and quality.
* Collaboration: Work closely with study teams and functional lines to ensure successful delivery of clinical trials.
* Technical Expertise: Leverage technical skills to drive innovation and improvement in data management and quality.
About the Role:
* Main Accountabilities:
* Provide DM leadership across assigned trials.
* Act as the Trial Data Manager where needed.
* Demonstrate business understanding of compounds profile to identify and assist in successful application of data management processes.
* Provide feedback to assure well-written protocols and amendments.
* Recognize and resolve protocol issues that may impact database design, data validation, and/or analysis/reporting.
* Perform DM activities for start-up of a study, data handling plan, data review plan, and user acceptance testing (UAT).
* Manage local lab setup for the Clinical Database as applicable.
* Lead 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.
Requirements:
* Experience:
* At least 4 years' experience in Clinical Data Management.
* Skills:
* Strong collaboration and organizational skills.
* Proven ability to successfully manage simultaneous trials and meet deadlines.
* Excellent understanding of clinical trials methodology, GCP, and medical terminology.
* Proven ability to interrogate and view data through various programming/GUI techniques.
Benefits:
* Commitment to Diversity & Inclusion: We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
* We offer a competitive salary and benefits package, including opportunities for professional growth and development.