Ppd In Office And Remote Work Values

Daily Duties at Ppd In Office And Remote:

Managed the operations of the clinical administration team, coordinated the clinical administrative functions of projects, and provided regulatory document technical expertise to multiple clinical research trials Allocated personnel hours and coordinated clinical research responsibilities in accordance with the company’s goals and objectives, managed and maintained Clinical Administration budgets, including out of scope tasks, adhered to project budget, and escalated potential project financial impacts to appropriate management Coordinated review of regulatory documents for proper and accurate content prior to submission to the Project Manager, central IRB, Regulatory Affairs, and/or the client Ensured clinical research management timelines and deliverables were met as specified by the Project Manager and client Assisted in ensuring audit ready files and contributed to company, client, and federal regulatory requirements and audit responses as needed Assisted in determining training needs and implementation of the clinical administration department Provided input in performance appraisals and reviews as requested

What they like about Ppd In Office And Remote:

Working for a company with an emphasis on social values and helping society is a clear and important priority for you - a critical factor in who you choose to work for. In contrast to other factors, you place an organization's reputation for fairness and concern for the community above most other aspects of the company. As you search for a new job opportunity, it is usually possible to find out if the company is involved in the community and/or if it is addressing problems and issues in society. Pay special attention to non-profit organizations and those specifically involved in social action. Moreover, speaking with current and former employees should enlighten you to perceptions of the fairness of the company's leaders and the treatment of employees.

Tags

Clinical Research, Business Management, Clinical Trials, Study Start Up, Sponsor Collaboration, Site Activation, Regulatory IRB/ EC, CLinTrak, goBalto, CTMS, Regulatory Submissions Manager

Skills

Lean Six Sigma Yellow Belt, Line Manager 10 years, Global Regulatory Submissions, Sponsor/ Client Facing, Drive Study Start Up Timelines, Problem solve to fast site activation, Postive Team Leader, Participate with Bid Defense , Kick Off, Investigator and Face 2 Face Meetings, Risk escalation and mitigations

These are some of the questions we asked our climbers about their experiences with Ppd In Office And Remote: