Senior Clinical Data Manager – Oncology

Job not on LinkedIn

🔥 19 minutes ago

🇨🇦 Canada – Remote

💵 $130k - $140k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 20%

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Lifelancer

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2020

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Pre Seed Round on 2022-03

Consulting • Healthcare • Logistics

Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.

📋 Description

• Lead clinical data management studies involving healthy volunteer and patient populations, multi-site studies, complex protocols, client management, or reduced timelines • Own data management deliverables from study start-up through database lock • Develop project documentation, system setup, data entry, and data validation procedures • Build timelines with Project Managers or FSP Leads to meet contracted milestones • Lead data-focused internal project team meetings and coordinate deliverables across EDC Design, SAS Programming, Statistics, and PK • Identify risks and mitigations and communicate data-driven discussions to achieve database lock dates • Coordinate receipt and inventory of data from clinical sites and vendors • Ensure projects follow protocols, global harmonized SOPs, GCP standards, DMPs, and scope of work • Maintain client relationships, review satisfaction surveys, and implement action plans and process improvements • Track scope changes and secure Sponsor approval • Provide leadership, mentorship, coaching, training, and performance feedback to data management staff • Reconcile clinical databases against safety, laboratory, and third-party data • Utilize local laboratory systems and batch data load facilities • Support new business opportunities, bid defense meetings, audits, and sponsor-facing Biometrics activities • Contribute to SOP development and maintain accurate work records • Keep stakeholders informed about project progress, budgets, scope changes, and timeline impacts

🎯 Requirements

• University / college degree; relevant work experience equating to a bachelor's degree accepted in lieu • Relevant and equivalent experience may be accepted in lieu of educational requirements • English required for speaking, writing, and reading • 8 years of combined early or late-stage DM experience • Minimum 2 years of direct sponsor management experience • At least 2 years of technical mentoring experience • 3–5 years of Oncology experience • Experience handling customer negotiations and managing Scope of Work and budgets • Thorough knowledge of clinical trial processes, data management, clinical operations, biometrics, and supporting system applications • Working knowledge of CRO regulatory obligations and relationships with pharmaceutical/biotechnology companies • Ability to adhere to project productivity metrics and timelines • Ability to mentor junior department members and provide SME guidance on data management practices • Experience representing data management in bid defense meetings • Four or more years of Electronic Data Capture experience preferred • University / college degree in life sciences, health sciences, information technology, or related subjects preferred • Knowledge of Fortrea’s organization and SOPs preferred

🏖️ Benefits

• Potential travel for cross-site support or training needs, meetings up to 10% of the time, with up to 50% of that time requiring an overnight stay • Compensation considers skills, prior relevant experience, applicable degrees/certifications, internal equity, and market data