Clin Data Mgr I - Lisbon

Clin Data Mgr I - Lisbon
Empresa:

Covance


Lugar:

Lisboa


Clin Data Mgr I - Lisbon

Detalhes da Vaga

Job Overview:

Covance is currently looking to recruit experienced Project Data Managers for our Biometrics group. Candidates with significant prior experience and a proven track record in delivering on projects will be considered for the Project Data Manager role. Home based or Office based role.
Serve as the technical leader on all data management aspects for project(s) including stait-up, maintenance, and completion activities.
Develop [Global] Data Management Plans and Quality Management (QM) Plans that will deliver accurate, timely, consistent, and quality clinical data.
Identify and implement solutions to project data management issues and concerns, including proactive prevention strategies based on metrics and forecasts.
Coordinate and participate i n the development of the clinical data model and/or database design and annotate the CRF (eCFR) according to these specifications.I monitoring conventions.
Interact and collaborate with other project and specialty team members (clinical, programming, statistics, CDM technical suppo1t, drug safety, etc.) to support the set-up, maintenance, and closure of the data management aspects of the project to ensure consistent, cohesive data handling and quality.
Coordinate the development and testing of data management systems edit I data validation checks) diagnostics) and special listings I procedures used as tools for the data review and discrepancy management activities.
Review data acquisition conventions and data review guidelines I diagnostic specifications consistent with the clinical data model, [statistical] analysis plans, and CRF (eCRF) completion
Serve as the project and client liaison including management and provision of project specific data management status, cycle time, and productivity metrics.
Advanced planning and risk management for projects (issue escalation, resource management).
Assist with goal creation and performance review assessment for data review project staff.
Ensure project staff are trained and adhere to project-specific, global, standardized data management processes.
Support achievement of project revenue and operating margin for data management activities to agreed targets.
Identify areas for process and efficiency improvement and implement solutions on assigned projects.
Maintain technical data management competencies via pa1ticipation in internal and external training seminars.
Oversee the technical pe1formance of the data review project staff on achieving client satisfaction through delivery of quality data, on-time and on-budget.
Develop and maintain strategic client relationships and receive client satisfaction surveys and implement appropriate action plans as necessary.
Support business development for data management time and cost estimates and prepare and present to potential clients on global data management capabilities.
Perform other duties as assigned by management.
Review literature and research technologies/procedures for improving global data management practices.
REQUIREMENTS:
University/college degree (life science, pharmacy or related subject preferred), or certification
In a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
Additional relevant work experience will be considered in lieu of formal qualifications.
Broad knowledge of drug development processes.
Understanding of global clinical development budgets and relationship to productivity targets.
Knowledge of effective clinical data management practices.
Knowledge of time and cost estimate development and pricing strategies.
Thorough knowledge of TCH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing
Relevant work experience in data management with technical supervisory experience to include data management, clinical operations, and knowledge of several therapeutic areas.
Demonstrated skills for technical management of staff exceeding 5 employees.
Financial management of gross revenues
Excellent oral and written communication and presentation skills.
In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical I biotechnological companies.
Ability to lead by example teams on project strategies and achievement of department goals, objectives, and initiatives and to encourage team members to seek solutions.
Demonstrated managerial and interpersonal skills
Education/Qualifications:

University/college degree (l ife science, pharmacy or related subject preferred), or certification
in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
Additional relevant work experience will be considered in lieu of formal qualifications.
Broad knowledge of drug development processes.
Understanding of global clinical development budgets and relationship to productivity targets.
Knowledge of effective clinical data management practices.
Knowledge of time and cost estimate development and pricing strategies.
Thorough knowledge of TCH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing
Experience:

Minimum five (5) years relevant work experience in data management with approximately one (1)year technical supervisory experience to include data management, clinical operations, and knowledge of several therapeutic areas.
Demonstrated skill for technical management of staff exceeding 5 employees.
Financial management of gross revenues in excess of $250K per year.
Excellent oral and written communication and presentation skills.
In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
Working knowledge of the relationshi p and regulatory obligation of the CRO industry with pharmaceutical I biotechnological companies.
Ability to lead by example teams on project strategies and achievement of depa11ment goals, objectives, and initiatives and to encourage team members to seek solutions.
Demonstrated managerial and interpersonal skills


Fonte: Neuvoo1_Ppc


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