Clinical Research Associate
- Novartis
- 1 - 2 Years
- Hyderabad
- 3 years ago
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Job Description
Job Description :With over 400 active trials in 5 hub countries, Novartis GDO Trial Monitoring (TMO) is committed to delivering end-to-end clinical operations within country to make the clinical trial process more efficient and patient-friendly. We bring together and manage all aspects of clinical trial operations to meet milestones in terms of quality, cost, and delivery time in order to better serve our patients. We develop strategies to optimally deploy resources as well as manage performance, budgets, and contractors. TMO is a proactive learning organization focused on collaboration and individual development to foster a synergistic environment. We rise to meet the challenges of the future by utilizing the latest digital technologies and data while optimizing risk to transform trials and improve lives. TMO is in search of those who are passionate about applying their experience to reimagine clinical trial operations and ultimately improve the lives of patients.
Position Purpose:
Experienced specialists performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of assigned clinical trials.
Is responsible to deliver data within timelines and required quality standard, responsible for adherence to monitoring procedures in accordance with GCP and ICH, local regulations and SOPs.
Major Accountabilities:
Monitors patient data and study-related information related to clinical study sites and clinical trial participation.
Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into data validation plan.
Provides timely and accurate monitoring of patient data and study-related information from source documents, research records, and site visits where applicable.
May monitor study sites and audit facility selection.
Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial
Performs site Initiation Visit, ensures site personnel is fully trained on all trial related aspects
Applies company policies and procedures to resolve a variety of issues
Frequent internal company and external contacts.
Represents organization on specific projects
Contributes to some cost center goals and objectives
Is the frontline liaison between Novartis and sites to ensure successful collaboration, site engagement and meeting Novartis expectation on milestone and deliveries
Deliver customer satisfaction results for internal and external customers
Delivery of Clinical Trials to quality standards and agreed timelines
Adherence to Novartis policy and guidelines and external regulations
How this role will Impact our purpose:
This role will be responsible for overseeing & monitoring trial related activities at the site, thereby ensuring robust site management and overall quality & data integrity at the clinical trial sites.
Minimum requirements :
Operations Management and Execution Project Management Cross Cultural Experience
Bachelors degree in any specialization. (Desirable) Bachelors in Pharma/ Life Science.
Minimum 1 to 2 years of relevant experience as CRA.
Fluent in both written and Spoken English.
Why consider Novartis
799 million. Thats how many lives our products touch. And while were proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more peoples lives
We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where youre given opportunities to explore the power of digital and data. Where youre empowered to risk failure by taking smart risks, and where youre surrounded by people who share your determination to tackle the worlds toughest medical challenges.
Imagine what you could do at Novartis!
Commitment to Diversity & Inclusion:
Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential.
Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network
Click below link to apply
https://jobs.brassring.com/TGnewUI/Search/home/HomeWithPreLoadPageType=JobDetails&partnerid=13617&siteid=5260&Areq=326850BR
Employement Category:
Employement Type: Full timeIndustry: Pharmaceutical
Functional Area: Pharmaceutical
Role Category: Clinical Research Associate
Role/Responsibilies: Clinical Research Associate
Contact Details:
Company: Novartis HealthcareLocation(s): Hyderabad
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Novartis
A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes us one of the most rewarding employers in our field.
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