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.:

Working in an organization that is technologically advanced, creative, and innovative is critical in your assessment of hiring companies. Less important to you are stability of the organization, the length of time an organization has been in business, and the business' plans for the future. You prefer a fast-moving company that will take risks to achieve its goals and objectives. The length of time the company has been in business is irrelevant. Maintaining status quo is unnecessary. You thrive on change, uncertainty and the upside of potential business risks, especially those associated with innovation. Stability for the long haul is not nearly as important as is working in an atmosphere that is charged with a sense of urgency and constant change.

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.: