Senior Manager, Clinical Data Management

Scorpion Therapeutics; United States; Remote; USD 140,000 - 200,000; Full time

Job summary

Takeda is seeking a Senior Manager, Clinical Data Management to lead a multidisciplinary team focused on clinical trial data management. The role aims to ensure trials are compliant with GxP and regulatory standards while achieving quality benchmarks.

You will oversee timelines and budgets, provide strategic guidance, and engage with internal and external stakeholders at various management levels. Remote role based in Massachusetts with flexible scheduling.

Qualifications

• Bachelor’s or Master’s degree with relevant CRO/pharma experience.
• Experience in clinical data management under GxP standards and regulatory compliance.
• Proven ability to lead cross‑functional teams and manage budgets/timelines.

Responsibilities

• Lead a multidisciplinary team in data management for clinical trials.
• Oversee project timelines, budgets, and stakeholder communications.
• Drive process improvements and present findings to senior management.

Skills

Data management

Regulatory compliance

GxP experience

CRO experience

Education

Bachelor's degree

Master's degree

Tools

SAS

SQL

EDC systems

Job description

Senior Manager, Clinical Data Management at Takeda

Overseeing a team responsible for developing and optimizing clinical data management processes.

Primary objectives include ensuring clinical trials are conducted efficiently, compliant with regulatory standards, and aligned with quality benchmarks.

Responsibilities

• Responsibilities involve managing a multidisciplinary team, overseeing project timelines and budgets, providing strategic guidance, and engaging with internal and external stakeholders at various management levels.
• The role also entails process improvement, training, and presenting findings.

Qualifications

• Qualifications include a bachelor's degree with 6+ years or a master's with 3+ years in CRO or pharmaceutical settings, with proficiency in complex clinical trial data management, GxP, and regulatory compliance.
• High-value specifics include work in clinical trials for pharmaceutical or biotech products, focusing on data management within regulated environments.

Location

The role is based remotely in Massachusetts with potential for flexible scheduling; no travel requirements specified.