Ppd Inc. Work Values

Daily Duties at Ppd Inc.:

• Monitored investigator sites, with particular ability of managing complex studies and/or challenging sites, ensured the accuracy and validity of eCRF entries • Performed and coordinated assigned aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of investigational products. • Identify, compose, and execute Corrective and Preventive Action plans (CAPAs) at site level as appropriate. • Recommend processes to Clinical Management that optimize the use of project resources • Provided mentoring and support to less experienced members of the project team and advice on training and quality issues. • As a certified accompanier, conducted Routine Performance Visits and Training Authorization Visits for new/experienced PPD CRAs. • Assisted colleagues with site visits and site calls, when needed. • Served as resource to team members with protocol, source document, CTMS, regulatory, data entry, and query resolution questions and issues. • Reviewed and approved team member monitoring visit reports for submission to Sponsor. • Developed collaborative relationships with investigative sites and Sponsor company personnel. • Developed study specific training materials for team members and sites.

What they like about Ppd Inc.:

Organizations with strong, centralized leadership are particularly attractive to you. You require a work environment with leadership that aggressively seeks to expand and grow the business and does so in a visible and decisive manner. In general you prefer to work in an environment in which there is a strong link between leadership, its actions, and a strong set of company-wide values.

Tags

CCRA, Florida, southeast, oncology, manager, IMPACT, RAVE, Phase I, Phase II, Phase III, CTMS, audit, CRA, clinical, research, associate, senior, experienced, management

Skills

Clinical Trial Management, Audit Response, Clinical Trial Management Systems, Electronic Data Capture, Contracts and Budgets - Creation and Management, Monitoring, Pharmacokinetics and Pharmacogentics, Investigator Payments - Schedule and Management, Data Lock Timelines, Recruitment Plans and Contingencies, Monitoring Plan Development and Execution, Corrective and Preventive Action Plan(s) - CAPA(s), Blinded Trial Management, Oral and IV Drug Accountability, Informed Consent Development

These are some of the questions we asked our climbers about their experiences with Ppd Inc.: