Novo Nordisk Clinical Research Job For Pharma – Apply Online
Clinical Research Associate – Pipeline
Category: Clinical Development
Location: Bangalore, Karnataka, IN
Department: Clinical Medical Regulatory (CMR)
Clinical Research Associate – Pipeline Requisition
You are applying to be part of the Novo Nordisk Talent Pool. We are currently interviewing for this role, but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, please submit your CV.
Joining our pipeline means that you will be considered as a potential match for all current and upcoming CRA roles. By applying, we’ll match your profile on a continuous basis against all suitable positions to ensure you don’t miss out on a life-changing career. When an opportunity arises, we will reach out and invite you for an interview. We will keep your application for six months ensuring the best opportunities to provide a solid match for open positions. If you want to be considered for CRA positions, we look forward to receiving your application.
Do you want to be a part of a high-performing team in Novo Nordisk that plays a critical role in driving the success of the business? Do
you have what it takes: the right drive, a sharp mind, customer orientation, openness, and focus on what matters, and a genuine interest in working with people? If you find challenges inspiring and want to drive innovation within a multifaceted and inspiring working environment, you may be our new CRA for the Clinical Medical Regulatory team based at Pan India. If you have what it takes to be a part of the Novo Nordisk team, Apply now!The position
The Clinical Research Associate (CRA) is the primary point of contact between site staff and Novo Nordisk. In this role, the CRA acts as an ambassador for the company. As a CRA you will be responsible for:
- Taking leadership of site management for the selection (if applicable) and initiation of sites as well as conduction and closing activities of the appointed studies in compliance with local regulations, ICH-GCP, NN procedures, and protocol requirements to ensure data quality and study subject protection.
- The CRA is responsible for recruitment at the site level. The CRA thereby delivers results that have a direct impact on the successful completion of the clinical program.
- Coordinating with CRM and RTM and communicates to them progress and critical issues that may impair trial progress. In some cases, the CRA may have direct contact with the ITM.
- Efficient and accurate site selection visits (as appropriate including analysis of site logistics, site performance/quality indicators).
- Accountability for patient recruitment strategies, including implementation of mitigation actions.
- Visiting trial sites regularly in accordance with the protocol to perform monitoring activities required.
- Proactive use of IT Systems (e.g., IMPACT, EDC) for preparation and conduct of site visits as well as source data verification in collaboration with the data management/logistics team.
Qualifications
To be successful in this role, you should have the following qualifications:
- You should be a graduate in Medicine, Science, Pharmacy, or another relevant field preferred.
- Certified in ICH-GCP trained is preferred.
- Additional qualification in clinical research would be preferred.
- 2 – 4 years of experience as a Clinical Research Associate.
- Experience in 1-2 multinational clinical trials phase 2-3 from site initiation till site closure preferred.
About the department
The Clinical Medical Regulatory (CMR) department is responsible for running all clinical development activities from initial planning of clinical trials towards authority submission. We investigate patients’ reactions to new drugs, compare them to existing products, and run a set of pre-specified trials in human beings. Our department provides resources, processes, and competencies in Biostatistics and Programming, Clinical Reporting, Data Management, Epidemiology/Real World Evidence, and Clinical Pharmacology to all development projects. We support all development projects by providing means for process alignment and optimization, competency development, knowledge sharing, and training with regard to trial planning and trial execution across trial management and medical staff.
Working at Novo Nordisk
Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world, and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and collaboration of our more than 63,000 employees around the world. We recognize the importance of the unique skills and perspectives our people bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk, we’re working toward something bigger than ourselves, and it’s a collective effort. Join us! Together, we go further. Together, we’re life changing.
Contact
To submit your application, please upload your CV and motivational letter online (click on Apply and follow the instructions).
Deadline
12th Aug 2024
Link to Original Notification to apply
Keywords: Clinical Research Associate, Pipeline, Novo Nordisk, CRA, Biostatistics, ICH GCP. Novo Nordisk Clinical Research Job For Pharma – Apply Online. Subscribe to Rasayanika for the latest chemistry and Pharma job openings, follow us on Facebook and Telegram and subscribe to our youtube channel for the latest updates on chemistry and Pharma jobs and much more.
