Clinical Data Manager

The Clinical Data Manager, will participate in various clinical data management activities required to ensure that data captured in a few clinical trials undertaken, or managed by Innovaderm, are collected, managed and reported clearly, accurately and securely. In addition, this position is required to conduct all these activities in conformance with applicable regulatory requirements, industry guidelines, and Innovaderm standard operating procedures (SOPs) while respecting Innovaderm’s commitment to sponsor’s requirements and timelines.


This role will be perfect for you if:


  • You enjoy working with a Canadian-owned mid-sized CRO where you can build professional relationships with your colleagues at all levels
  • You bring previous experience in managing data management
  • Dermatology is a therapeutic area you enjoy or want to learn more about




  • Develops the electronic case report form (eCRF) specifications (including data capture screens and edit check specifications) needed to build a study-specific clinical database/electronic data capture (EDC) system.
  • Programs and maintains the clinical database.
  • Is responsible for the validation and testing of the clinical database (e.g. User Acceptance Testing).
  • Is responsible for the development of eCRF completion guidelines and other training material required to train site users and monitors.
  • Conducts training for site users/monitors on the clinical database.
  • Develops data transfer agreements and specifications with vendors providing external data (e.g. laboratory results).
  • Conducts reconciliation between external data and data in the EDC system to ensure consistency, including reconciliation with sponsor safety databases for adverse events/serious adverse events data (if needed).
  • Provides support to study team in the development of external systems capturing clinical data, e.g. ePRO or IWRS, and ensuring that any data transfer requirements between these systems and EDC are documented and tested appropriately.
  • Develops the development of the data management plan (DMP), and other clinical data management related documentation. 
  • Ensures ongoing data review/cleaning during study conduct and also during preparation for database lock/close.
  • Codes medical terms in the clinical database, as required.
  • Generates data listings and reports needed for data review by the project manager (or other study team members) in preparation for database close/lock.
  • Monitors study status (e.g. enrollment, CRFs monitored/approved, etc.) on an ongoing basis and provides data status reports to the project team, as needed.
  • Ensures that data management documentation is complete and up-to-date in the trial master file (TMF).
  • Activates/de-activates new users in the clinical database in response to requests from the project manager and maintains records of such requests.
  • Responds to users requiring assistance with the EDC system.
  • Archives the clinical database and related documents.
  • Mentors and trains a Clinical Data Coordinator.
  • Oversees the vendor to ensure timelines and deliverables meet sponsor, protocol and regulatory requirements



  •  B.Sc. or in a related field of study;
  • M. Sc. Or in a related field of study is an asset;



  • At least 2 years of clinical data management experience in clinical research in the biotechnology, pharmaceutical, or contractual research organization (CRO) industry;
  • Understanding of the drug development process and of applicable regulations, including Good Clinical Practices, ICH Guidelines;
  • Extensive experience working with clinical trial EDC systems (Medrio, Rave, Inform), and/or database structures, including demonstrated skills in database programming;


Knowledge and skills

  • Good understanding of CDISC SDTM/CDASH standards;
  • Highly organized and detail-oriented with effective project planning and time management skills.
  • Excellent problem solving abilities;
  • Strong verbal and written communication skills in English; French is an asset.
  • Ability to work in a fast-paced environment with demonstrated agility to juggle and prioritize multiple competing demands;
  • Knowledge of MedDRA and WHODrug dictionaries.
  • Good knowledge of good clinical practices, and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines.


The work environment 


At Innovaderm, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability and responsiveness. We offer a stimulating work environment and attractive advancement opportunities. 


In this position, you will be eligible for the following perks: 

  • Flexible work schedule 
  • Permanent full-time position 
  • Complete benefits (medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, social activities) 
  • Offices near public transportation (Sherbrooke metro station or Saint-Laurent metro station) 
  • Possibility of working from home in accordance with company policies and public health directives 
  • Ongoing learning and development 


About Innovaderm  

Innovaderm is a contract research organization (CRO) specialized in dermatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Innovaderm continues to grow and expand in North America and Europe. 


Innovaderm is committed to providing equitable treatment and equal opportunity to all individuals. As such, Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request. 

Innovaderm only accepts applicants who can legally work in Canada. 

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