Clinical Trial
6 months ago
As a Clinical Research Associate, you will be responsible for managing and monitoring clinical trials. You will work closely with investigators to ensure that all aspects of the study are conducted according to protocol and in compliance with regulatory requirements. Your tasks will include preparing and reviewing study documents, ensuring adherence to timelines, conducting site visits to monitor safety data, and coordinating communication between study sites and sponsors. You must have excellent attention to detail as well as strong organizational skills in order to manage multiple studies simultaneously. Additionally, you must possess the ability to analyze complex medical data accurately while maintaining complete confidentiality at all times. The role of a Clinical Research Associate is crucial in ensuring the success of clinical trials by upholding ethical research standards while obtaining accurate results that can lead us closer towards discovering new treatments or cures for diseases.
**Job Types**: Full-time, Permanent, Fresher
**Salary**: ₹121,676.13 - ₹502,091.59 per year
**Benefits**:
- Health insurance
- Provident Fund
- Work from home
Schedule:
- Day shift
- Morning shift
- Rotational shift
Supplemental pay types:
- Commission pay
- Performance bonus
- Yearly bonus
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Clinical Trials Assistant
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Lead SAS Programmer for Clinical Trials
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Operational Excellence Manager
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Clinical Trial Veeva Tech Lead: IT Expertise
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Clinical Research Associate
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Clinical Research Associate
6 months ago
Pune, Maharashtra, India Ascentrik Research Pvt Ltd Full time**Job Type - Fresher or Internship level** Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe. **Responsibilities**: **1. Assist in Protocol Development**: -...
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Clinical Research Associate
6 months ago
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Clinical Research Trainer
2 months ago
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Clinical SAS Programmer
6 months ago
Hinjawadi, Pune, Maharashtra, India BridgeOceans Technologies Inc Full timeAs a **Clinical SAS Programmer **you will Ssupport all programming activities which will required for the data analysis of the clinical trials and create standard datasets (SDTM) and analysis datasets (ADaM) and generate reports of the form Tables, Graphs and Listings as applicable. - Planning and working with the clinical programming group to schedule...