Sr Central Monitoring Analyst II

Company Name:PPD Development, L.P.Position Title:Senior Central Monitoring Analyst IILocation:929 North Front Street, Wilmington, NC 28401

Summary of Duties: Act as a subject matter expert and interdepartmental and client liaison for data analytics activities. Ensures performance of assigned reviews with high quality, on-time results with more complex analyses or deeper root cause analyses to connect related signal to risks. Leads the design and setup of study specific tools and centralized monitoring plan for data review. Support budget management. Ensures reviews are completed on-time, on-budget, with a high quality. Assists with report development, delivers reports, and leads centralized monitoring meetings. Contributes to risk assessment through the completion of the department risk assessment tools. Participates in the cross-functional risk assessment review meetings and contributes to overall risk planning. Duties may be performed remotely.

Company Name:PPD Development, L.P.Position Title:Senior Central Monitoring Analyst IILocation:929 North Front Street, Wilmington, NC 28401

Summary of Duties: Act as a subject matter expert and interdepartmental and client liaison for data analytics activities. Ensures performance of assigned reviews with high quality, on-time results with more complex analyses or deeper root cause analyses to connect related signal to risks. Leads the design and setup of study specific tools and centralized monitoring plan for data review. Support budget management. Ensures reviews are completed on-time, on-budget, with a high quality. Assists with report development, delivers reports, and leads centralized monitoring meetings. Contributes to risk assessment through the completion of the department risk assessment tools. Participates in the cross-functional risk assessment review meetings and contributes to overall risk planning. Duties may be performed remotely.

Qualifications: Bachelor’s in Life Sciences, Medical Science, or related field and five (5) years’ experience as a Data Liaison, Clinical Review Associate, Clinical Research Associate, or related role. Five (5) years’ experience in: MS Office (Word, Excel, PowerPoint); Extracting pertinent information from standard study documentation; Plan, monitor, and manage demands within a project environment; Advanced Excel skills including macro programming; and SDTM mapping. One (1) years’ experience in: Understanding of project protocol, project documentation, including Centralized Monitoring Plan; and Advanced analytical Spotfire dashboards.

Qualifications: Bachelor’s in Life Sciences, Medical Science, or related field and five (5) years’ experience as a Data Liaison, Clinical Review Associate, Clinical Research Associate, or related role. Five (5) years’ experience in: MS Office (Word, Excel, PowerPoint); Extracting pertinent information from standard study documentation; Plan, monitor, and manage demands within a project environment; Advanced Excel skills including macro programming; and SDTM mapping. One (1) years’ experience in: Understanding of project protocol, project documentation, including Centralized Monitoring Plan; and Advanced analytical Spotfire dashboards.