Clinical Process Specialist

Clinical Process Specialist #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 # Qualifications Bachelor's Degree Bachelor s degree in clinical, life sciences, mathematical sciences, or related field, or nursing qualification. Req Requires minimum of 2 years of relevant work experience or equivalent combination of education, training and experience. Fresher with Medical or Allied medical degree. Experience in clinical research field preferred. Experience level may vary based on customer specific requirements. Advanced knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements. i.e. International Conference on Harmonisation - Good Clinical Practice (ICH GCP) and relevant local laws, regulations and guidelines, towards clinical trial conduct. Good Clinical system expertise. Strong written and verbal communication skills including good command of English language. Results and detail-oriented approach to work delivery and output. Understanding of clinical/medical data. Good motivational, influencing, coaching skills. Ability to work on multiple projects and manage competing priorities. In depth therapeutic and protocol knowledge. Strong organizational and problem-solving skills. Effective presentation skills. Demonstrated ability to deliver results to the appropriate quality and timeline metrics. Ability to work across cultures and geographies with a high awareness and understanding of cultural differences and maintain effective working relationships with coworkers, managers and clients.