Jobs at Novotech

The core responsibility for this position is as a member of Novotech’s Data Management group. The Senior Clinical Data Manager’s (SCDM’s) role is to control all aspects of data management and to ensure compliance with Good Clinical Data Management Practices (GCDMP). As an experienced CDM, the SCDM provides mentorship to junior staff and can also provide support to the project manager. Expectation of being a leader within the department by leading process improvements, new initiatives as well as training for junior colleagues.

Novotech is a global full-service clinical Contract Research Organization (CRO).

• Determination of project feasibility from a data management perspective. Understand the requirements of the project agreement and scope to ensure that Novotech performs these services as required. If full service, then collaborates with PM to ensure appropriate mitigation and contingencies are initiated
• May act as Project Manager for “stand-alone” data management projects.
• Participates in project team meetings as required.
• Input into the preparation of RFPs in liaison with BD and the clinical team.
• Liaison with the project team and client for preparing and maintaining Data Management Plans.
• Responsible for all aspects of data management including:
• Design and review of database structure, validation rules and consistency checks
• Operation of Clinical Data Management Systems
• All data cleaning/validation tasks
• Development of all key Data Management Documents
• Liaison with client companies / monitoring staff as appropriate, ensuring effective study communication with internal and external stake holders
• Liaison with external service providers on Data Management projects as appropriate
• Assist in the development of protocols as required.
• Supervision and training support for junior and contract Data Management staff as required.
• Adherence to company Quality Policy and procedures as applicable to carrying out job responsibilities.
• Active contribution in Data Management process improvement including identification of and participation in process improvement initiatives.
• Perform accurate study financial projections and maintain monthly project financials.
• Ensure changes in scope are identified and actioned accordingly
• Provide expert assistance and input into internal cross-functional projects including clinical research and regulatory affairs, as assigned.
• Project management of internal IT-based company projects as assigned (e.g. intranet development, client database applications etc.).
• Active contribution to company business development initiatives, including involvement in the implementation of data management plans for business development in the company in general.
• Participation in industry fora (conferences, professional association committee work, etc) as a means of professional development as well as promotion of Novotech’s image in industry.

• Graduate degree in a clinical or life sciences related field
• 8+ years of experience in a similar role within the research, pharmaceutical industry, or a related domain
• Technical Skills: Hands-on experience with EDC systems: Medidata Rave and Veeva CDMS