Clinical Research Associate
- Rianshi Developers
- 99 Positions
- Bengaluru
- 4 days ago
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Job Description
- Monitoring Clinical Trials: CRAs conduct site visits to verify that trials are following the study protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
- Data Management: They oversee the collection, documentation, and entry of data into electronic data capture (EDC) systems, ensuring accuracy and completeness.
- Participant Safety: CRAs are responsible for ensuring the safety and well-being of trial participants.
- Regulatory Compliance: They ensure that trials adhere to all relevant regulations and guidelines, including those from regulatory bodies like the FDA.
- Communication and Liaison: CRAs serve as a primary point of contact between the sponsor, investigators, and other stakeholders, facilitating communication and resolving issues.
- Site Management: They may be involved in identifying and qualifying potential investigators, setting up research sites, and managing study supplies.
- Report Preparation: CRAs contribute to the preparation of reports, including interim monitoring reports, and may be involved in the development of publications based on trial data.
A Clinical Research Associate (CRA) plays a crucial role in clinical trials, ensuring they are conducted ethically and in accordance with regulations. CRAs monitor trials, manage data, and ensure participant safety. They act as a key liaison between sponsors, research sites, and other stakeholders.
Key Responsibilities:
Employement Category:
Employement Type: Full timeIndustry: Pharma / BiotechRole Category: Medical TranscriptionFunctional Area: Not SpecifiedRole/Responsibilies: Clinical Research AssociateContact Details:
Company: Rianshi DevelopersLocation(s): Bengaluru+ View Contact
Keyskills: research procedures communication problem-solving coordinating
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