Aimee Wang Email & Phone Number

Singapore, Sg

Singapore, Sg

朝阳区, 北京市, Cn

Process management，staff management，trial management

Rahway, New Jersey, Us

-Develops career plans for direct reports, makes work assignments, conducts periodic skill assessments as well as annual performance appraisals, coaches for performance, provides ongoing feedback on performance, provides rewards and recognition, and sets priorities-Provides developmental opportunities for direct reports, including challenging growth assignments. Prepares promotion recommendations. Ensures direct reports receive appropriate training and mentoring to be successful in their assignments-Participates in the recruitment process -Maximizes staff effectiveness by working with direct reports to ensure a realistic workload that supports value-added work and work-life balance, estimating length and difficulty of tasks and projects, anticipating and adjusting for obstacles and setbacks, and elevating issues to the appropriate management level -Assume specific functional leadership responsibilities for business deliverables assigned to direct reports and supervised staff on project-Increases team and functional effectiveness by supporting functional efforts to simplify and standardize procedures to the greatest extent possible, sharing best practices and leading continuous improvement efforts under the direction of Associate Director-Manages performance -Conducts management and functional area meetings, contributing expertise when necessary through formal or informal presentations.-Keeps abreast of process and technology changes both within and outside of Merck that may impact staff.-May participate in initiatives beyond functional area (e.g. cross-functional initiatives, etc.).

Rahway, New Jersey, Us

The main point of contact to the study team, representing the end to end data management perspective at the trial level and accountable for all deliverables. Develops detailed project plans for the collection, review, and cleaning of all clinical data for assigned trials within a specific drug / vaccine program. Serves as project manager of all clinical data management activities for trials as assigned and performs and manages the following tasks: -Project planning, initiation, execution, change control, and closing. -Project team development, project team leadership, meeting management, and resource coordination. -Risk management planning (i.e., risk identification, analysis, response planning, monitoring, and control), including escalation as necessary. -Management of customer/stakeholder expectations; facilitation of cross-functional decisions.Defines trial-level requirements for quality data collection and validation at the trial level. -Reads and interprets the clinical protocol from a clinical data management perspective. -Engages with key stakeholders and subject matter experts to assess complexity, define trial-level data management requirements and inputs (including timing), and confirm all data management deliverables and services required for a trial. -Creates and maintains key DM deliverables such as eCRF, Data validation plan, eCRF entry guideline, Data Management Plan, etc.Manages trial-level data quality and completion of database lock and post-lock activities: -Monitors overall status and quality of data being collected during in-life. -Ensures activities required to achieve database lock (or data extraction) are completed by appropriate, responsible functional area. -Ensures timely archival of trial data and documentation.

Rahway, New Jersey, Us

Coordinates protocol-specific DPL mentoring, leads the protocol-specific DPL Network, works with the Data Management Services (DMS) Lead and Project Data Manager (PDM) to ensure that the data review plan is correctly implemented and DMC status is communicated to the project team. Coordinates and mentors the DMC protocol data review team. Communicates with sites and country CRAs to ensure visits are promptly entered and queries are promptly escalated and resolved. Responsible for ensuring protocol-level compliance of standard key performance indicators according to process expectations.Operates within a data management center (DMC); reviews data entered by investigational site staff. Uses exception reports to identify data inconsistencies or departures from eCRF Entry Guidelines. raises queries with site and confirms resolution.

Master, Pharmaceutics

Bachelor, Pharmacy