Senior Analyst, Data Quality

Calyx • Needham, MA

4d • $75,000 - $90,000 • Onsite

About The Position

The Senior Analyst, Data Quality is a highly detail-oriented and collaborative individual who ensures the integrity, consistency, and accuracy of pre-clinical data across multiple modalities. This person plays a key role in supporting the Senior Data QC Analyst Manager by providing leadership within the QC Analyst team, ensuring high-quality data review across modalities, and collaborating cross-functionally to meet project goals. This role focuses on process improvements to enhance efficiency and data accuracy. The Senior Analyst, Data Quality will collaborate cross-functionally with the Project Management (PM), Image Analysis (IA), Lab, and Study Director (SD) teams to ensure high quality pre-clinical data for sponsors/clients.

Requirements

• Confidence with nuclear medicine-related modalities
• Confidence with documentation related to animal handling, radiochemical procedures, and study design
• Strong analytical, organizational skills, and attention to detail
• Exceptional communication abilities in both written and verbal formats
• Ability to troubleshoot and resolve issues in a cross-functional environment
• Ability to manage multiple priorities with precision, and meet specified timelines
• Must be able to work effectively both independently and as a team
• Proven experience managing and leading mentoring colleagues.
• Proven line management and leadership management
• Experience using tools to communicate progress to Stakeholders.
• Master's degree with several years of experience in imaging or pharmaceutical project management, or bachelor’s degree (BS or BA) in a relevant field (e.g., Biomedical Engineering, Medical Physics, Chemistry, or Pharmacology) with 5+ years of equivalent experience
• Knowledge and experience in pre-clinical in vivo imaging applications (MRI, PET, SPECT, or CT) including understanding of theory and familiarity with data acquisition, analysis techniques, and quality control
• English: Fluent

Responsibilities

• Support the team by resolving complex scientific data integrity issues that may arise
• Provide guidance to QCA I, and QCA II team members in scientific training; support the training of new hires
• Identify issues and as needed, work with team member(s) to resolve issues affecting project scope, quality, effort, risk, and timelines
• Implement best practices in quality control and review of raw, pre-processed, and analyzed data of all modalities and therapeutic areas for accuracy, consistency, and completeness in alignment with internal standards and project requirements
• Review reporting to ensure consistency in data presentation across studies within a Sponsor Program or Alliance Agreement
• Identify QC bottlenecks and gain insights into data generation processes
• Collaborate with the Analysis and Software teams to streamline and automate manual QC workflows, increasing throughput and reducing human error
• Contribute to the development of SOPs, templates, and internal guidelines for quality control processes
• Carryout any other reasonable duties as requested.

Benefits

• Medical, Dental and Vision benefits for you and your family, including Flexible Spending Accounts (FSA)
• Paid time off policy including holidays and sick time
• Internal growth and development programs & trainings
• 401(k) program, life & accident insurance and disability insurance

What This Job Offers

• Job Type: Full-time
• Career Level: Senior