Centralized Study Specialist I

Centralized Study Specialist I #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #pharmaindustry #doctor #phd #oncology #drugdevelopment #cra #biotechnology # University/College Degree (Life Science preferred), or certification in an allied health profession from an appropriate accredited institution (Ex: Nursing certification, Medical or laboratory technology) and 05-08 years of work experience in clinical research, including a strong working knowledge of the ICH-GCP guidelines and all other applicable guidelines and regulations. In addition to above, Candidates without life sciences background but with relevant domain knowledge or experience may be considered, if deemed appropriate for specific tasks and activities. Experience Minimum Required: - Years of experience in the job discipline: 05-08 Years - Years of experience in other professional roles: 00-05 Years - Other required work-related experiences: - Demonstrated ability to plan, prioritize, organize and communicate effectively. - Demonstrated ability to pay attention to detail. - Strong interpersonal skills with ability to work well with others. - Ability to deliver consistent high quality of work. - Strong interpersonal skills. - Ability to Influence others. - Ability to facilitate meetings. - Ability to lead process improvement initiatives