Full-Time

Senior Lead Data Manager

Updated on 7/21/2026

Altasciences

Altasciences

1,001-5,000 employees

Integrated CRO for early-phase drug development

Compensation Overview

$65.7k - $87.5k/yr

Laval, QC, Canada + 1 more

More locations: Overland Park, KS, USA

Remote

Remote in the United States (Overland Park, KS) or Canada (Laval, Quebec).

Category
Biology & Biotech (1)
Required Skills
Word/Pages/Docs
Excel/Numbers/Sheets
PowerPoint/Keynote/Slides

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Requirements
  • Bachelor's Degree in programming, health-related sciences, or relevant field and 5-8 years of Data Management experience. Experience may be considered in lieu of education.
  • Excellent verbal and written communication skills.
  • Professional attitude and strong interpersonal skills.
  • Ability to work well with a multi-disciplinary team of professionals.
  • Client-focused approach to work.
  • Flexible attitude with respect to work assignments and new learning.
  • Ability to prioritize workload.
  • Superior attention to detail.
  • Understanding of clinical research and the relationship of Data Management in the clinical study process.
  • Proven history of continuous improvement.
  • Strong technical aptitude and ability to adapt to multiple data management platforms.
  • Strong knowledge of electronic data capture (EDC) clinical data management systems.
  • Good computer skills (Microsoft Word, Excel, and Power Point) and ability to understand and adapt to various information technology (IT) systems.
  • Fluency in English is an essential requirement for the position.
Responsibilities
  • Follow department and company standard operating procedures (SOPs), forms, templates and policies. Provide feedback and update these guidelines as needed.
  • Act as the primary Data Management contact for the client and project team, proactively managing sponsor and interdepartmental expectations.
  • Develop strong client relationships that are driven by consistent study delivery in terms of quality and timeliness.
  • Develop, review, and maintain all study Data Management documentation.
  • Coordinate with Database Developers to ensure effective database build and timely go-live to meet the needs of the project.
  • Ensure the clinical database adheres to Clinical Data Acquisition Standards Harmonization guidelines allowing for optimal SDTM dataset programming. Suggest design for standard and non-standard data collection, identify any gaps in data collection, and challenge collection of unnecessary data.
  • Define electronic case report form (eCRF) and edit check specifications to support data collection and analysis required per protocol.
  • Take responsibility for and guide effective quality control (QC) review and user acceptance testing (UAT) of the clinical database prior to its release into production, including oversight of staff performing these tasks.
  • Delegate and collaborate with Data Managers on data management cleaning activities including listing review, issuing and closing queries, and external vendor data reconciliation per protocol, department and client standards, and International Conference on Harmonisation (ICH)
  • Good Clinical Practice (GCP) guidelines within the timelines expected by the client and project team.
  • Ensure data are properly reviewed in accordance with the Data Management Plan (DMP) and department and sponsor guidelines and that cleaning is effective and timely.
  • Track eCRFs to ensure appropriate updates and that all missing or discrepant data are queried appropriately. Monitor key study metrics and provide status reports to the sponsor and project team.
  • Maintain the Data Management documentation for the trial master file (TMF) according to department and Project Management processes.
  • Provide input on study timelines, identify risks, and communicate mitigation strategies to the Project Manager.
  • Provide input into improving the efficiency of data management tasks.
  • Lead and participate in intradepartmental or interdepartmental process and quality improvement initiatives.
  • Oversee direct reports as assigned.
  • Mentor and train other team members and/or develop training materials as needed.

Altasciences provides an integrated CRO that handles the full early‑phase drug development path, from preclinical testing through clinical proof of concept and into manufacturing. Its approach combines discovery support, safety testing, clinical trial execution, and in‑house manufacturing to run programs under one roof. This contrasts with competitors that require pharma and biotech clients to source services from multiple vendors, adding complexity and risk; Altasciences streamlines the process by coordinating all steps. The company aims to help innovator drug programs move quickly and efficiently, delivering integrated data to de‑risk decisions and speed progression to later stages.

Company Size

1,001-5,000

Company Stage

Early VC

Total Funding

$6.7M

Headquarters

Laval, Canada

Founded

1976

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Simplify Jobs

Simplify's Take

What believers are saying

  • Strategic Certara partnership embeds biosimulation to enable earlier proof of mechanism and refined dosing.
  • RegulatoryFlow AI from Evidence Matters automates one-third of nonclinical reports to expedite timelines.
  • 258 active hiring postings in 2025 signal capacity expansion supporting integrated model and growth.

What critics are saying

  • Certara integration enables sponsors to make go/no-go decisions earlier, reducing later-phase trial volume and revenue.
  • AI tools like RegulatoryFlow and Instill erode preclinical consulting margins and program management revenue by 20–30%.
  • Smaller CROs expanding early-phase with lower pricing may force loss of 15–25% of Phase I contracts in 6–12 months.

What makes Altasciences unique

  • Fully integrated CRO/CDMO spans preclinical to clinical proof of concept under one supplier.
  • Proprietary Acceleration Platform reduces timelines by 25–40% via parallel execution and single-point contact.
  • Eight global facilities and 1,800+ employees deliver 98% on-time delivery for early-phase trials.

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Benefits

Health Insurance

Dental Insurance

Vision Insurance

401(k) Company Match

Paid Vacation

Paid Sick Leave

Paid Holidays

Employee Assistance & Telehealth Programs

Remote Work Options

Growth & Insights and Company News

Headcount

6 month growth

4%

1 year growth

4%

2 year growth

8%
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