Job title: Clinical Trial Administrator

Company: Novo Nordisk

Job description: Job description Department – CMR Location – Bangalore Are you experienced Clinical research professional and passionate about clinical trials? Does being part of a growing, yet dynamic environment excite you? If yes, then you may be the one we are

Job description Department – CMR Location – Bangalore Are you experienced Clinical research professional and passionate about clinical trials Does being part of a growing, yet dynamic environment excite you If yes, then you may be the one we are looking as Clinical Trial Administrator (CTA) for Novo Nordisk India, Bangalore. The position As a CTA, you will provide support to the CDC Project Managers and CRAs in relevant aspects of trial activities in CDC-India (start up, execution and closure) and facilitate timely clinical project deliverables of required quality by Novo Nordisk India in accordance with Good Clinical Practice (GCP) guidelines and in line with local regulatory requirements. The scope of CTA activities for a particular clinical trial may vary with respect to countries sponsored. The activities start post country allocation and ends after study documents are sent for central archival post completion of trial. In this role your main responsibilities will be customization and translations of study documents, Health Authority and Ethics Committee submissions, contracts, auxiliary and trial product supplies management, support for arranging global/local investigator meeting and other departmental meeting or related activities, study payments, systems, filing of study documents (electronic and physical copies) and any tasks assigned as per project needs in compliance with local regulations, ICH- GCP, Novo Nordisk procedures and protocol requirements. Qualifications Below are the required skills. Graduate in Science, Pharmacy or Medical. Additional Qualification in Clinical Research would be preferred. At least 1 year of experience in Clinical Research or in similar job profile such as CRC/CTA. You are required to be trained in ICH-GCP guidelines and if applicable certification is also preferred. Should have very good communication skills (both written and oral), able to work efficiently with team and as individual, eagerness to learn and attention to detail. Demonstrated ability to plan, execute and follow-up of trial related activities (applicable for this position). About the department Novo Nordisk is a Denmark based multinational with leadership in diabetes. Novo Nordisk India affiliate office is located in Bangalore & has more than 1400 people working across the country in various functions. The CTA position reports directly to the Clinical Research Manager . Workingat Novo Nordisk At Novo Nordisk, westriveforexcellence.Yousharethesamepassion andcommitmentas ouremployeesin ourjourneytomake adifference to patients’ lives.Inexchange, weofferyouthechanceof alifetimeto work with extraordinary talent and benefit from unmatched opportunities forprofessionaland personal development. Contact To submit your application, please upload your CV and motivational letter online (click on Apply and follow the instructions). Internal candidates are kindly requested to inform their line Manager before applying. Deadline: 15 Jun 2022 We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

Expected salary:

Location: Bangalore, Karnataka

Job date: Sat, 11 Jun 2022 22:41:49 GMT

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