Cra Ii
1 week ago
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That’s our vision. We’re driven by it. And we need talented people who share it. If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP. The role: - Independent, proactive work to set up and monitor studies, complete reports and maintain documentation - Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions - Balancing sponsor generated queries - Taking responsibility for study cost efficiency - Preparation and review of study documentation and feasibility studies for new proposals - Potential to assist in training and mentoring fellow CRAs You will need: - 18 months+ of monitoring experience in phase I-III trials as a CRA - College degree in medicine, science, or equivalent - Previous monitoring experience in medium-sized studies, including study start-up and close-out - Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data - Excellent written and verbal communication - Ability to work to tight deadlines - Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license Benefits of Working in ICON: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know
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Clinical Research Associate Ii
18 hours ago
Bengaluru, Karnataka, India Emmes Global Full timeOverview: **CRA II** **India Remote/Ahmedabad/Bengaluru/New Delhi** Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical...
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Clinical Research Associate Ii
1 week ago
Bengaluru, Karnataka, India Emmes Global Full timeOverview: **Job Posting Title** **India Remote/Bangladesh** Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research...
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Clinical Research Associate I
1 week ago
Bengaluru, Karnataka, India Emmes Global Full timeOverview: **Clinical Research Associate** **India Remote/Bengaluru** Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical...
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Centralised Clinical Team Lead II
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Bengaluru, Karnataka, India Fortrea Full time ₹ 12,00,000 - ₹ 36,00,000 per year. Individual Contributor Trip Report Review responsibilities: Reviews trip reports and works closely with project teams towards implementation of best trip report practices; revising applicable project plans where needed. Proactively identifies risks in the trip reports and communicates any trends, outstanding issues, safety concerns to the study team....
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Frontend Sde I
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Bengaluru, India BigShyft Full time**What will you do**: - Strong knowledge of JavaScript fundamentals, Object-oriented programming, and Web concepts. - Experience with React.js, and build tools like Web pack. - Follow code quality and best practices at Newton School. - Take end-to-end ownership of products. Ideate product requirements with the team and drive them from design to...
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Clinical Research Associate Ii
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Bengaluru, Karnataka, India Fortrea Full time**Summary of Responsibilities**: - Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. - Conducts site monitoring responsibilities for clinical trials according to Fortrea’s...
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Centralized Study Spec Ii
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Bengaluru, India Labcorp Full timeFollow all applicable departmental Standard Operating Procedures and Work Instructions. Complete required trainings according to required timelines. Complete day-to-day tasks ensuring quality and productivity. Manage project and technical documentation in an appropriate manner. Provide administrative and technical support to internal departments and teams as...
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Centralized Trip Report Reviewer-ii
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Bengaluru, India Labcorp Full timeManagement of complex projects under direction of a Project Manager / Director as assigned. Ensure site monitoring responsibility for clinical studies are conducted according to Covance Standard Operating Procedures, ICH Guidelines and GCP. Work Closely with project teams in implementation of best TRR practices & applicable project plans as assigned...
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Prm Associate Ii
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Bengaluru, India ICON plc Full timeAt ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives. ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing...
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Centralized Study Associate Ii
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Bengaluru, Karnataka, India Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
