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Sr. Clinical Data Manager

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

United Kingdom, Canada

Offer summary

Qualifications:

1-2 year post-secondary certification, 3-5 years in Clinical Data Management.

Key responsabilities:

Lead data management activities for projects
Oversee day-to-day data management operations

Alimentiv SME https://alimentiv.com/

201 - 500 Employees

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Job description

JOB SUMMARY:

Responsible for leading, planning and execution of all data management activities for assigned projects, ensuring focus on data integrity, validity, reliability in accordance with standard processes, sponsor guidelines, industry best practices and regulatory standards. Act as coach, mentor and/or Subject Matter Expert within the department, aiding Manager in process improvements, issue escalation and training development and delivery. Support the department and company in achieving objectives and strategic goals.

Project Support

Serve as the Lead Data Manager and primary contact responsible for overseeing day-to-day data management activities from study start-up through final database lock, including, but not limited to:

Creation and maintenance of the Data Management Plan

Development and design of Case Report Forms (CRFs)

Develop Database Build specifications and coordinate database build and testing activities with database programmers

Define and test edit checks

Perform data review and query generation/resolution

Track study progress and issue periodic status reports

Process/reconcile electronic data received from other data sources, e.g. CIMS, Safety database, labs, IRT

Oversee database lock and transfer process.

Coordinate and supervise the day-day work of Data Management (DM) staff assigned.

Train and mentor assigned employees on data management procedures and guidelines.

Participate/lead internal/sponsor meetings as required, working directly with the assigned project manager and team to provide data management support.

Ensure approved study documentation is maintained and properly stored in the trial master files.

Manage project resources per budget and within expected timeframes.

Develop or assist with the project training development and delivery, for investigators, clinical sites, project teams and sponsors on data collection processes, tools and/or equipment as required.

Act as point of escalation for data related issues and queries.

Department Support

Contribute to the continuous improvement of DM and the wider organization through information sharing, training and education.

Promote and be an advocate of DM internally and externally.

Coach, mentor and/or train peers, contribute to peer selection, performance evaluation, peer orientation and project communications.

May participate in and/or lead the development, review and implementation of processes, policies, SOPs/WI’s and associated documents affecting DM.

May participate in and/or lead DM and cross functional working groups.

May supervise Data Management staff.

QUALIFICATIONS

Applicants should have a minimum of a one to two year post-secondary certification in a relevant field of study, and 3-5 years of related work experience in Clinical Data Management with ongoing training. CCDM designation is considered an asset.

WORKING CONDITIONS

Home-based