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Please Note:We have flexibility to hire at either DML I OR DML II level for this role!Job Purpose:The Data Management Lead l provides leadership in all aspects of Data Management.
Manages timelines for study data deliveries, including Go-Live, Interim Deliveries, and Final DB Lock.
Collaboration with the relevant functions (Clinical, Biostatistics, Database Programming, Medical, Medical Writing etc.)
across all geographies.
Data Management's single point of contact to ensure that the contracted Data Management deliverables are being met – specifically in terms of timeliness, financial management and quality.The Data Management Lead l works under the guidance of their Line Manager and may receive additional direction/support from an experienced Data Management Lead or Subject Matter Experts.
They may work as a co-DML with an experienced DML or work independently on less complex trials.Key Accountabilities:Cross-functional DM Leadership through Database Set up, Conduct and Study Close-Out• Manage and coordinate the integration and utilization of all ancillary systems as appropriate.• Highlight issues/risks to delivery by understanding interdependencies.
Support mitigations and drive to resolution with cross-functional stakeholders as part of Risk Management Plan.• Review and analyze metrics to derive meaningful summary of study health and trends.• Review of the Master Services Agreement, Service Level Agreement, and/orcontract to manage toward sponsor-specific metric targets/Key PerformanceIndicators.• Host and attend cross-functional meetings.
Prepare Meeting Agendas andMinutes, comply to action and decision logs.Bid Pursuits and Proposals• Support experienced DML in Bid Pursuit preparation meetings.• Provide input on DM slides, as appropriate.Project Quality Management and Compliance• Ensure compliance to Standard Operating Procedures, ICH/GCP Guidelines.• Maintain inspection-ready Trial Master File.• Identification of quality issues, ensuring they are raised in relevant systemand closed according to requirements.• Prepare for and participate in audits and inspections for internal, sponsor,and regulatory agencies.• Support and implement Corrective/Preventive actions for study, and worktoward alignment across Parexel as appropriate.Project Financial and Resource Management• Ensure appropriate project level resourcing of staff and staff assignments.Identify and request functional staff necessary for the project team.• Regular review and update of DM resources to ensure alignment withcontracted budget, project resource forecast, actuals, and demand, utilizingthe necessary systems and tools.• Determine and resolve the root cause of DM-related project variance in atimely manner, including negotiating/raising changes in scope.Company Initiatives• May provide Data Management functional input, considering the impact ofthe initiative and the impact on Data Management and Parexel as a whole.• May support other functions as appropriate to provide meaningful functionalfeedback on the initiative.• Ensure Parexel-requested information entered into management systems isaccurate and regularly updated.Training• Maintain training compliance as per Job Roles assigned, including On-the-Job training.• Deliver Project Specific Training to internal DM team.• Address training needs, as per Development Goal/s identified.Required Knowledge and Experience:• Experience in clinical research industry or similar field (Clinical Data Management specific experience / skills preferred)• Proven record of coordinating and supporting project teams• Basic understanding or willingness to learn and apply Parexel financial tools, reports and processes for management of project financials with regards to forecasting, revenue recognition, scope of work and department budget for assigned projects• Understanding of or willingness to learn Clinical Study Team roles outside of Data Management• Full understanding or willingness to learn and apply relevant ICH-GCP Guidelines, local regulatory requirements and Parexel SOPs and study specific procedures• Awareness of/or willingness to learn SDTM/CDISC/CDASH standards• Awareness/potential prior experience in Clinical Trial/Data Management Systems (e.g.
InForm, Rave, Veeva, DataLabs) and Microsoft Office products.• Demonstrates technical aptitudeEducation:Bachelor's degree and /or other qualifications in a science or clinical related industry.Skills:• Ability to lead and collaborate with global teams.
Motivate/guide virtual teams across multiple time zones and cultures to work effectively• Negotiation skills and ability to influence, in order to achieve mutually beneficial results• Good interpersonal, oral and written communication skills, using concise phrasing tailored for the audience with a diplomatic approach• Learning ability and knowledge sharing approach; swift understanding of technologies and new processes• A flexible attitude with respect to work assignments and new learning; ability to adjust rapidly to changing environments• Basic presentation skills• Customer focus to interact professionally and respectfully within Parexel and all external colleagues to build rapport and trust• Commitment to first-time quality, including a methodical and accurate approach to work activities• Time management and prioritization skills, in order to meet objectives and timelines• Evidence of strong problem-solving skills, including capability to make appropriate decisions in ambiguous situations, ability to conduct root cause analyses• Ownership and accountability relative to Key Accountabilities in Job Description• Ability to travel as required• Written and oral fluency in English
