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BriefCase

Test Job 4 in Test Company 4

Test Job 4

Test Company 4 4+ weeks ago
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Job Summary Job Title: Clinical Research Associate (CRA) Job Type: Full-Time Job Overview: We are looking for a skilled Clinical Research Associate (CRA) to join our team. In this role, you will be responsible for managing and monitoring clinical trials to ensure compliance with regulatory requirements, protocols, and quality standards. The ideal candidate will have experience in clinical research and a strong understanding of GxP (Good Clinical Practice) guidelines. Key Responsibilities: Monitor and manage clinical trials, ensuring that they are conducted in compliance with protocols, regulatory requirements, and ethical standards. Perform site qualification, initiation, monitoring, and close-out visits in accordance with the study plan. Ensure that clinical sites maintain accurate and complete study documentation, including patient records, consent forms, and clinical data. Act as the main point of contact between clinical sites, sponsors, and other stakeholders. Verify that clinical trial sites are following the protocol and regulatory guidelines, addressing any issues or discrepancies that arise. Collaborate with cross-functional teams, including investigators, site staff, and project managers, to ensure smooth trial operations. Ensure the integrity of data and safety of trial participants through continuous oversight and monitoring. Conduct risk assessments and report findings to stakeholders. Provide training and guidance to site staff on study protocols and procedures. Prepare and review clinical trial-related documentation, including informed consent forms, case report forms (CRFs), and progress reports. Contribute to the preparation of clinical trial progress reports for regulatory authorities and other relevant parties. Required Qualifications: Bachelor s degree in Life Sciences, Nursing, Pharmacy, or a related field. 2+ years of experience as a Clinical Research Associate, with a proven track record in monitoring clinical trials. Knowledge of GxP guidelines, ICH (International Council for Harmonisation), and local regulatory requirements. Strong understanding of clinical trial phases and the drug development process. Experience with clinical trial management systems (CTMS), eCRF (electronic case report forms), and other related software. Strong organizational, communication, and interpersonal skills. Ability to manage multiple tasks simultaneously and meet deadlines. Attention to detail and a commitment to ensuring patient safety and data integrity. Preferred Qualifications: Clinical Research Coordinator (CRC) certification or Clinical Research Associate certification (e.g., ACRP or SOCRA). Experience in therapeutic areas such as oncology, cardiology, or neurology. Familiarity with electronic data capture (EDC) systems. Experience with global clinical trials and regulatory submissions. Ability to travel to clinical sites as required by the project. Benefits: Competitive salary and performance-based incentives. Health and wellness programs, including insurance. Opportunities for career development and professional certifications. Collaborative work environment with a focus on personal and professional growth. Flexible working hours and remote work options. How to Apply: If you are passionate about clinical research and want to contribute to the development of groundbreaking therapies, please submit your resume and a cover letter outlining your experience and qualifications.
Salary : ?7,00,000 - ?9,00,000
Skills Required :
Clinical Trials, Data Collection
Qualification :
Bachelor's in Biology
Experience Required :

Minimum 2 Years

Vacancy :

2 - 4 Hires

Skills Required :

Clinical Trials, Data Collection

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