Clinical Trial Administrator

Clinical Trial Administrator #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 # About Novotech Novotech is internationally recognized as the leading independent and fullservice contract research organization CRO in the Asia Pacific region. We provide a wide range clinical development services across all research phases and therapeutic areas and have been instrumental in the success of hundreds of Phase I IV clinical trials throughout the Asia Pacific. Our people are one of our key strengths. We value our people and recognize the work they do. We are lucky to have the best people and talent from across the Asia Pacific region work together to deliver to clinical trial success for our clients. About the position We have an exciting new opportunity and are seeking a committed, adaptable and driven individual looking to build a career as a Clinical Trials Administrator CTA based in Bangalore. This role has been designed specifically for an individual interested in building a career in clinical trials project administration and coordination. The Clinical Trial Administrator is a key member of the project team and the role has an established professional career path for high performers. Core Responsibilities On a day to day basis the CTA provides pivotal inhouse administrative and operational support to Clinical Research Associates and Project Managers on Novotech clinical trials. Key responsibilities include assisting clinical staff in the collection and maintenance of essential documents, management of the trial master file, attending meetings and taking minutes, tracking of study progress and management of the distribution of studies supplies. Required Professional Experience and Qualifications 12 years clinical research experience having CTA knowledge and an interest in life sciences or healthcare experience working in the pharmaceutical, CRO or healthcare industry would be preferable Superior written and verbal communication skills Highly proficient in computer programs including Microsoft Office and experience with managing multiple databases Excellent attention to detail with a strong focus on reaching a quality outcome Demonstrated ability to meet deadlines and manage time and workflow effectively A proactive approach to work and a willingness to help improve inefficiencies An ability to work flexibly as part of a team and with a variety of internal and external customers Qualifications in business or administration would also be advantageous Opportunities and benefits At Novotech, we seek and nurture people with exceptional talent. We are committed to providing our people with regular internal and external training, a competitive bonus structure and a supportive work environment. We are also focused on providing our people with a wide variety of career growth and development opportunities. For more information about where your next career step at Novotech might take you, visit http:novotechcro.comnovotechcareers