Join Our Dynamic Team as a Clinical Data Manager II at Allucent

At Allucent, we empower small to medium biopharmaceutical enterprises to effectively maneuver through the intricacies of clinical trials, delivering transformative treatments to global communities in need. We are thrilled to announce an opening for a Clinical Data Manager II (DM II) to enhance our dedicated team, offering flexible hybrid or remote working options.

Role Overview

As a Clinical DM II, you will undertake vital responsibilities within the Allucent Data Management department. Your role will span from database design and setup to ensuring data integrity meets stringent quality and regulatory standards for analysis and reporting. This position provides an outstanding opportunity to influence the success of clinical trial processes and improve patient outcomes worldwide.

Main Responsibilities

Your tasks at Allucent will include:

• Assisting in various DM-related tasks and collaborating closely with Lead DMs and other data management professionals.
• Acting as a primary DM contact for all relevant internal and external parties, managing communications and updates effectively.
• Monitoring task progress against budgets and forecasts, and managing resources based on project demands.
• Leading the setup of clinical study databases, including eCRF design and database validation.
• Developing and reviewing project-specific documents like Data Management Plans (DMPs) and data validation plans.
• Ensuring the accuracy and integrity of clinical data through meticulous review and validation processes.
• Spearheading the creation of data cleaning strategies and managing data releases and reconciliations.
• Providing training and support during User Acceptance Testing (UAT) and for new EDC system users.
• Leading Quality Reviews and preparing documentation for audits.

Required Qualifications

To be successful in this role, you will need:

• A background in life sciences or healthcare, supplemented by at least 2 years of experience as a Clinical Data Manager.
• Proficiency in drug development, clinical research, and knowledge of ICH-GCP, GDPR/HIPAA, and other regulatory standards.
• Strong familiarity with EDC systems, IRT, and eCOA, along with a solid understanding of medical terminology and database management.
• Experience with CDISC conventions, particularly CDASH and TAUG models.
• Excellent communication, project management, and analytical skills.

Why Choose Allucent?

Working at Allucent provides numerous benefits:

• A competitive benefits package and salary structured per location.
• Flexible working hours and the option for hybrid or remote work arrangements.
• Opportunities for professional development, leadership, and career advancement.
• Access to internal and external training resources to enhance your skills.

Embark on a rewarding career path with Allucent, where innovative therapies and patient welfare intersect with clinical expertise and career fulfillment. Explore the potential to drive change in a supportive and dynamic environment.

Candidates interested in this impactful role as a Clinical Data Manager II in Canada are invited to apply. Our hybrid work model blends onsite collaboration with remote flexibility, promoting balance and productivity. Join us in transforming patient lives, one trial at a time.

Disclaimer

All recruitment communications and processes are managed directly by Allucent's Talent Acquisition team. Please respect our policy of not accepting unsolicited resumes from third-party recruiters.

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